<?xml version="1.0" encoding="utf-8"?>
<XML>
		<JOURNAL>
<YEAR>2015</YEAR>
<VOL>9</VOL>
<NO>3</NO>
<MOSALSAL>3</MOSALSAL>
<PAGE_NO>73</PAGE_NO>
<ARTICLES>


				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>مقایسه متابولیت های وابسته به انرژی در دوره حوالی زایش در میش های آبستن تک قلو و دوقلو از نژاد لری-بختیاری</TitleF>
				<TitleE>Comparison of energy related metabolites during peri-parturition period in single and twin-bearing Lori-Bakhtiari ewes</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55282.html</URL>
                <DOI>10.22059/ijvm.2015.55282</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: The Lori-Bakhtiari sheep breed is one of the most common native breed in the south-western parts of Iran. The peri-parturition period (2 weeks before to, 2 weeks after parturition), is generally of critical importance regarding the health, production and profitability of the ewes. OBJECTIVES: This study was carried out to compare the serum concentrations of glucose, non-esterified fatty acid (NEFA), β-hydroxybutyrate (BHBA), cholesterol, blood urea nitrogen (BUN) and calcium (Ca) during peri-parturition period in 30 single and 30 twin-bearing Lori-Bakhtiari ewes. METHODS: All blood profiles were determined in healthy ewes on days 14, 7 prepartum, and days 7 and 14 postpartum. RESULTS: Serum glucose levels were lower in twin-bearing ewes, compared to single-bearing ewes on prepartum and day 7 after lambing. Serum NEFA, BHBA and cholesterol levels were higher in twin-bearing ewes compared to single-bearing ewes during the peri-parturition period. Lower serum Ca levels were recorded 7 days before and after parturition in twin-bearing ewes, compared to single-bearing ewes. CONCLUSIONS: The results showed that NEFA and BHBA recorded significant (p&lt;0.05) changes during the peri-parturition period in twin-bearing ewes. These significant differences could be related to increased metabolic demands of the fetuses in twin-bearing ewes. </CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه: نژاد لری-بختیاری یکی از متداولترین نژادهای بومی گوسفند در بخش‌های جنوب غربی ایران است. به طور کلی دوره حوالی زایش (از 2 هفته قبل تا 2 هفته بعد از زایمان) از نظر سلامتی، تولید و سودآوری میش‌ها اهمیتی بحرانی دارد. هدف: این تحقیق با هدف مقایسه غلظت سرمی گلوکز، اسیدهای چرب غیراستریفیه (NEFA)، بتا هیدروکسی بوتیرات (BHBA)، کلسترول، نیتروژن اوره خون (BUN) و کلسیم در دوره حوالی زایش در 30 رأس میش آبستن تک قلو و 30 رأس میش آبستن دوقلو از نژاد لری-بختیاری انجام گردید. روش کار: تمامی پارامترهای خونی در میش‌های سالم و در روزهای 14 و 7 قبل از زایمان و روزهای 7 و 14 بعد از زایمان اندازه گیری شد. نتایج: میزان گلوکز سرم در میش‌های با آبستنی دوقلو در مقایسه با میش‌های با آبستنی تک قلو در قبل از زایمان و روز 7 بعد از زایمان کمتر بود. مقادیر سرمی NEFA، BHBA و کلسترول در میش‌های آبستن دوقلو در دوره حوالی زایش بیشتر از میش‌های آبستن تک قلو بود. میزان کلسیم سرم در روزهای 7 قبل و بعد از زایمان در میش‌های با آبستنی دوقلو کمتر از میش‌های آبستن تک قلو بود. نتیجه گیری نهایی: نتایج نشان داد که تغییرات در میزان NEFA و BHBA در دوره حوالی زایش در میش‌های آبستن دوقلو معنی‌دار (05/0&gt;p) هستند. این تفاوت‌های معنی‌دار می‌تواند ناشی از افزایش نیازهای متابولیک جنین‌ها در میش‌های آبستن دوقلو باشد.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>149</FPAGE>
						<TPAGE>154</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>افشین</Name>
						<MidName></MidName>		
						<Family>رئوفی</Family>
						<NameE>Afshin</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Raoofi</FamilyE>
						<Organizations>
							<Organization>Department of  Internal Medicine, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>raoofi@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محسن</Name>
						<MidName></MidName>		
						<Family>جعفریان</Family>
						<NameE>Mohsen</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Jafarian</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Pathology, Faculty of Specialized Veterinary Sciences, Sciences and Research Branch, Islamic Azad University, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>m.jafariand@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>شهاب الدین</Name>
						<MidName></MidName>		
						<Family>صافی</Family>
						<NameE>Shahabeddin</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Safi</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Pathology, Faculty of Specialized Veterinary Sciences, Sciences and Research Branch, Islamic Azad University, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>safishahab@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمود</Name>
						<MidName></MidName>		
						<Family>وطنخواه</Family>
						<NameE>Mahmoud</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Vatankhah</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, Agriculture and Natural Resources Center, Shahre-Kord, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>vatankhah_mah@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Energy metabolites</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Lori-Bakhtiari sheep</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>peri-parturition period</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>twin-bearing</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Balıkcı, E., Yıldız, A., Gurdogan, F. (2007) Blood metabolite concentrations during pregnancy and postpartum in Akkaraman ewes. Small Rumin Res. 67: 247-251.##Edmondson, M.A., Pugh, D.G. (2009) Pregnancy toxemia in sheep and goats. In: Current Veterinary Therapy Food Animal Practice 5. Anderson, D. E., Rings, D. M.  (eds.). Saunders Elsevier, St. Louis, USA. p. 144-145.##El-Sherif, M.M.A., Assad, F. (2001) Changes in some blood constituents of Barki ewes during pregnancy and lactation under semi arid conditions. Small Rumin Res. 40: 269-277.##Fırat, A., Özpınar, A. (2002) Metabolic profile of pre-pregnancy, pregnancy and early lactation in multiple lambing Sakiz ewes 1. Changes in plasma glucose, 3-hydroxybutyrate and cortisol levels. Ann Nutr Metab. 46: 57-61.##Goff, J.P. (2009) Calcium, magnesium, and phosphorus: in Large Animal Internal Medicine, (4th ed.) Smith B.P.  (ed.). Mosby Elsevier, St. Louis, USA. p. 1369-1377.##Hamadeh, M.E., Bostedt, H., Failing, K. (1996) Studies on relevant metabolism parameters in blood plasma of highly pregnant and nonpregnant ewes. Berl. Munch. Tierärztl. Wochenschr. 109: 81–86.##Harmeyer, J., Schlumbohm, C. (2006) Pregnancy impairs ketone body disposal in late gestating ewes: Implications for onset of pregnancy toxemia. Res Vet Sci. 81: 254-264.##Henze, P., Bickhardt, K., Fuhrmann, H. (1994) The influences of insulin, cortisol, growth hormone and total oestrogen on the pathogenesis of ketosis in sheep. Deutsch. Tierärztl. Wochensch. 101: 61–65.##Moallem, U., Rozov, A., Gootwine, E., Honig, H. (2012) Plasma concentrations of key metabolites and insulin in late-pregnant ewes carrying 1 to 5 fetuses. J Anim Sci. 90: 318-324.##Moghaddam, G., Hassanpour, A. (2008) Comparison of blood serum glucose, beta hydroxybutyric acid, blood urea nitrogen and calcium concentrations in pregnant and lambed Ewes. J Anim Vet Adv. 7: 308-311.##Nazifi, S., Saeb, M., Ghavami, S.M. (2002) Serum lipid profile in Iranian fat-tailed sheep in late pregnancy, at parturition and during the post-parturition period. J Vet Med Ser A. 49: 9-12.##Radostits, O.M., Gay, C.C., Hinchcliff, K.W., Constable, P.B. (2007) Veterinary Medicine, (10th ed.) Saunders, Edinburgh, UK.##Rodriguez, M.N., Tebot, I., Bas, A., Niievas, C., Leng, L., Cirio, A., Le Bas, A. (1996) Renal functions and urea handling in pregnant and lactating Corriedale ewes. Can J Anim Sci. 76: 469-472.##Schlumbohm, C., Harmeyer, J. (2003) Hypocalcemia reduces endogenous glucose production in hyperketonemic  sheep. J Dairy Sci. 86: 1953- 1962.##Schlumbohm, C., Harmeyer, J. (2004) Hyperketonemia impairs glucose metabolism in pregnant and nonpregnant ewes. J Dairy Sci. 87: 350-358.##Schlumbohm, C., Harmeyer, J. (2008) Twin- pregnancy increases susceptibility of ewes to hypoglycemic stress and pregnancy toxemia. Res Vet Sci. 84: 286-299.##Schlumbohm, C., Sporleder, H.P., Gurtler, H., Harmeyer, J. (1997) The influence of insulin on metabolism of glucose, free fatty acids and glycerol normo- and hypocalcemic ewes during different reproductive states. Deutsch. Tierärztl. Wochenschr. 104: 359-365.##Shadnoush, G.H., Ghorbani, G.R., Edris, M.A. (2004) Effect of different energy levels in feed and slaughter weights on carcass and chemical composition of Lori-Bakhtiari ram lambs. Small Rumin Res. 51: 243-249.##Sigurdsson, H. (1988) The effects of flock, number of fetuses and age on some biochemical blood constituents in ewes in late pregnancy under field conditions.  J Vet Med Ser A.  35: 417-423.##Takarkhede, R.C., Gondane, V.S., Kolte, A.Y., Rekhate, D.H. (1999) Biochemical profile during different phases of reproduction in ewes in comparison to rams. Indian Vet J. 76: 205–207.##Vatankhah, M., Zamani, F. (2007) Phenotypic and genetic characteristics of longevity in Lori-Bakhtiari sheep. Biotechnol Anim Husb. 23: 323-329.##Vernon, R.G., Clegg, R.A., Flint, D.J. (1981) Metabolism of sheep adipose tissue during pregnancy and lactation. Biochem J. 200: 307-314.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>تآثیر تغذیه روغن کنجد بر عملکرد، فراسنجههای خون و تخمیر شکمبهای برههای پرواری</TitleF>
				<TitleE>Effect of sesame oil feeding on performance, plasma lipids and ruminal fermentation of growing lambs</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55283.html</URL>
                <DOI>10.22059/ijvm.2015.55283</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: In recent years, dietary fat supplementation has become a common practice and fat supplemented diets have had variable effects on animal performance and carcass characteristics. OBJECTIVES: This study was conducted to determine the effect of  increasing the levels of sesame oil on performance, rumen parameters and plasma lipid profile in finishing Chal lambs. METHODS: Eighteen male lambs were fed with control (C; without sesame oil) and the diets contained low level (LSO; 2.5%) and high level (HSO; 5%) of sesame oil. RESULTS: The addition of fat had no effect on dry matter intake (DMI), average daily gain (ADG), feed conversion ratio (FCR) and carcass weight. Treatments with sesame oil had no effect on rumen ammonia concentration and total protozoal count. Ruminal pH was numerically smaller (p=0.14) for control compared to lambs fed diets containing 2.5 and 5% sesame oil. Treatments had no effect on total VFA, acetate, butyrate, valerate and isovalerate concentrations. The propionate concentration decreased (p=0.04) by supplementation of sesame oil compared with the control. Total cholesterol (TC) and HDL increased and the tendency for VLDL and triglyceride (p=0.13) to increase was observed by treatment groups when compared with the control. Glucose concentration and LDL were not affected by treatment. CONCLUSIONS: Sesame oil had no effect on the performance and carcass weight of lambs but there was decrease in blood cholesterol concentration.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  در سالیان اخیر استفاده از مکمل‌های غذایی در جیره نشخوارکنندگان گسترش یافته است. در این زمینه استفاده از مکمل‌های چربی بر عملکرد تأثیرات متفاوتی داشته است. هدف: این مطالعه به منظور بررسی تأثیر سطوح مختلف روغن کنجد بر عملکرد، فراسنجه‌های خون و تخمیر شکمبه در بره‌های پرواری نژاد شال انجام شد. روش کار: هیجده رأس بره نر شال با  سه جیره آزمایشی حاوی مقادیر صفر (شاهد)، 5/2 و 5٪ روغن کنجد در طول دوره پروار تغذیه شدند. نتایج: افزودن مکمل چربی تأثیری بر میانگین خوراک مصرفی، میانگین افزایش وزن روزانه، ضریب تبدیل غذایی و وزن لاشه نداشت. همچنین اعمال تیمارهای آزمایشی تأثیری بر غلظت آمونیاک شکمبه و جمعیت پروتوزایی آن نداشت. افزودن روغن کنجد تأثیر معنی‌داری بر غلظت کل اسیدهای چرب فرار و همچنین غلظت اسیدهای چرب فرار استات، بوتیرات، والرات و ایزووالرات شکمبه نداشت. امام غلظت پروپیونات در جیره‌های حاوی روغن کنجد کمتر از تیمار شاهد بود (04/0=p). غلظت کلسترول و HDL در بره‌هایی که از جیره‌های حاوی روغن استفاده کردند، نسبت به بره‌های تیمار شاهد کمتر بود. غلظت گلوکز و LDL تحت تأثیر تیمارهای آزمایشی قرار نگرفت. نتیجه‌گیری‌نهایی: افزودن روغن کنجد تأثیری بر عملکرد و وزن لاشه بره‌های شال نداشت اما باعث کاهش معنی‌دار غلظت کلسترول خون شد.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>155</FPAGE>
						<TPAGE>161</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>هادی</Name>
						<MidName></MidName>		
						<Family>غفاری</Family>
						<NameE>Hadi</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Ghafari</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, College of Abouraihan, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>hadighafari@alumni.ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>علی اکبر</Name>
						<MidName></MidName>		
						<Family>خادم</Family>
						<NameE>Ali Akbar</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Khadem</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, College of Abouraihan, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>akhadem@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمد</Name>
						<MidName></MidName>		
						<Family>رضائیان</Family>
						<NameE>Mohammad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Rezaeian</FamilyE>
						<Organizations>
							<Organization>Department of Animal Health and Nutrition, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mrezaee@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>احمد</Name>
						<MidName></MidName>		
						<Family>افضل زاده</Family>
						<NameE>Ahmad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Afzalzadeh</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, College of Abouraihan, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>aafzal@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>داود</Name>
						<MidName></MidName>		
						<Family>شریفی</Family>
						<NameE>Davood</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Sharifi</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, College of Abouraihan, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>sdsharifi@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمدعلی</Name>
						<MidName></MidName>		
						<Family>نوروزیان</Family>
						<NameE>Mohammad Ali</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Norouzian</FamilyE>
						<Organizations>
							<Organization>Department of animal Science, College of Abouraihan, University of Tehran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>manorouzian@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>animal performance</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>cholesterol</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>finishing lamb</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>sesame oil</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>VFA concentration</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Beaulieu, A.D., Drackley, J.K., Merchen, N.R. (2002) Concentrations of conjugated linoleic acid (cis-9, trans-11-octadecadienoic acid) are not increased in tissue lipids of cattle fed a high- concentrate diet supplemented with soybean oil. J Anim Sci. 80: 847–861.##Castro, T., Manso, T., Mantecón, A.R.,  Guirao, J., Jimeno, V. (2005) Fatty acid composition and carcass characteristics of growing lambs fed diets containing palm oil supplements. Meat Sci. 69: 757–764.##Clinquart, A., Micol, D., Brundseaux, C., Dufrasne, I., Istasse, L. (1995) Utilisation des matieres grasses chez les bovinsa lengraissement. INRA Production Animal 8: 29–42.##Demirel, G., Wachira, A.M., Sinclair, L.A., Wilkinson, R.G., Wood, J.D., Enser, M. (2004) Effects of dietary n-3 polyunsaturated fatty acids, breed and dietary Vitamin E on the fatty acids of lamb muscle, liver and adipose tissue. British J Nutr. 91: 551–565.##Dohme, F., Machmuller, A., Estermann, B.L., Pfister, P., Wasserfallen, A., Kreuzer, M. (1999) The role of the rumen ciliate protozoa for methane suppression caused by coconut oil. Lett Appl Microbiol. 29: 187–192.##Doreau, M., Ferlay, A. (1995) Effect of dietary lipids on nitrogen metabolism in the rumen: A review. Livest Prod Sci. 43: 97–110.##Duckett, S.K., Andrae, J.G., Owens, F.N. (2002) Effect of high oil corn or added corn oil on ruminal biohydrogenation of fatty acids and conjugated linoleic acid formation in beef steers fed finishing diets. J Anim Sci. 80: 3353–3360.##Haddad, S.G., Younis, H.M. (2004) The effect of adding ruminally protected fat in fattening diets on nutrient intake, digestibility and growth performance of Awassi lambs. Anim Feed Sci Technol. 113: 61–69.##Hristovm, A.N., Vander Pol, M., Agle, M., Zaman, S., Schneider, C., Ndegwa, P., Vaddella, V.K., Johnson, K., Shingfield, K.J., Karnati, S.K.R. (2009) Effect of lauric acid and coconut oil on ruminal fermentation, digestion, ammonia losses from manure, and milk fatty acid composition in lactating cows. J Dairy Sci. 92: 5561–5582.##Ivan, M.,  Mir, P.S.,  Koenig, K.M.,  Rode, L.M., Neill, L.,  Entz, T.,  Mir, Z. (2001) Effects of dietary sunflower seed oil on rumen protozoa population and tissue concentration of conjugated linoleic acid in sheep. Small Rumin Res. 41: 215–227.##Kott, R.W., Hatﬁeld, P.G., Bergman, J.W., Flynn, C.R., Van Wagoner, H., Boles, J.A. (2003) Feedlot performance, carcass composition, and muscle and fat CLA concentration of lambs fed diets supplemented with safﬂower seeds. Small Rumin Res. 41: 11–17.##Lough, D.S., Solomon, M.B., Rumsey, T.S., Kahl, S., Slyter, L.L. (1993) Effects of high-forage diets with added palm oil on performance, plasma lipids, and carcass characteristics of ram and ewe lambs. J Anim Sci. 71: 1171–1176.##Manso, T., Castro, T., Mantecon, A.R., Jimeno, V. (2006) Effects of palm oil and calcium soaps of palm oil fatty acids in fattening diets on digestibility, performance and chemical body composition of lambs. Anim Feed Sci Technol. 127: 175–186.##Manso, T., Bodas, R., Castro, T., Jimeno, V., Mantecon, A.R. (2009) Animal performance and fatty acid composition of lambs fed with different vegetable oils. Meat Sci. 83: 511–516.##Marinova, P., Banskalieva, V., Alexandrov, S., Tzvetkova, V., Stanchev, H. (2001) Carcass composition and meat quality of kids fed sunflower oil supplemented diets. Small Rumin Res. 42: 219.##National research council (1985) Nutrient requirements of sheep. (6th ed.) National research council, National academy of sciences. Washington, DC, USA.##Saqhir, S., Jamal Abo, O., Omar, N., Ibrahim, G., Jihad, A. (2012) Performance and carcass characteristics of finishing black goat kids fed oil supplemented diets. Anim Feed Sci Technol. 175: 1–7.##Ueda, K., Ferlay, A., Chabrot, J., Loor, J.J., Chilliard, Y., Doreau, M. (2003) Effect of linseed oil supplementation on ruminal digestion in dairy cows fed diets with different forage concentrate ratios. J Dairy Sci. 86: 3999–4007.##Zinn, R.A. (1989) Inﬂuence of level and source of dietary fat on its comparative feeding value in ﬁnishing diets for steers: feedlot cattle growth and performance. J Anim Sci. 67: 1029–1037.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>تأثیر محیط کشت های مختلف بر روی بهینه سازی کشت اولیه سلول های عصبی برای ارزیابی مدل های برون تنی</TitleF>
				<TitleE>Effects of different culture media on optimization of primary neuronal cell culture for in vitro models assay</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55284.html</URL>
                <DOI>10.22059/ijvm.2015.55284</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: In vitro model studies are becoming increasingly popular for experimental research designs. They include isolation and expansion of cells of a particular tissue, such as the nervous tissue which contributes to understanding the underlying mechanisms in many pathologies. It enables  the scrutinization of intracellular signaling pathways responsible for cell death. OBJECTIVES: In the literature, there are different methods for the isolation and culture of rat embryonic cortical neurons. However, this study developed a feasible, rapid and easily performable method. METHODS: Isolation of neurons was performed without using enzymatic digestion. Primary cortical cultures neurite outgrowth and neuron numbers per field of common mediums were compared for neuronal cells isolation and expansion. In this study, three different culture mediums were considered: Medium I: Neurobasal medium, B-27 and L-glutamine; Medium II: DMEM, FBS and L-glutamine; and Medium III: DMEM/F-12, FBS and L-glutamine. RESULTS: High survival rate and number of neurons was obtained with the current method. The best neuronal growth was achieved by Medium I, while Medium II and III had moderate effect on the neurite outgrowth. CONCLUSIONS: Enzyme-free treatment was introduced and Medium I was used as an alternative method for optimal neuron isolation and expansion. The neuronal cultures are similar to nervous tissue in physiological aspects. Hence, Medium I is more similar to the in vivo condition compared to Mediums II and III.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  مطالعه مدل‌های برون‌تنی برای طراحی تحقیقات تجربی رو به افزایش است. از جمله این نوع مطالعات جداسازی و کشت سلول‌ها از بافت‌های مختلف مانند بافت‌های عصبی می‌باشد، که در شناخت مکانیسم‌های اساسی آسیب‌ها می‌تواند بسیار کمک کننده باشد و ما را قادر می‌سازد تا مسیرهای سیگنالینگ درون سلولی مسئول مرگ سلولی را به دقت مورد بررسی قرار دهیم. هدف: اگر چه تا کنون، روش‌های مختلفی برای کشت نورون‌های قشری جنین رت توصیف شده است. با این حال، مطالعه موجود روش عملی و سریعی را معرفی می‌کند که می‌تواند در این نوع مطالعات مورد استفاده قرار گیرد. روش کار: در این مطالعه، از سه محیط کشت مختلف، به ترتیبی که توضیح داده می‌شود برای جداسازی و کشت نورون‌ها در کشت اولیه قشری بدون استفاده از هضم آنزیمی استفاده گردید: محیط‌های مورد استفاده عبارت بودند از: محیط I: محیط نوروبازال، B-27 و ال-گلوتامین؛ محیط II: DMEM، FBS و ال-گلوتامین؛ و محیط III:رFBS،ز12-DMEM/F، و ال-گلوتامین. نتایج: میزان زنده مانی نورونی در این مطالعه بسیار قابل توجه بود و بهترین رشد نورونی در محیط I مشاهده گردید، در حالیکه محیط‌های II و III اثر متوسطی بر روی رشد نوریت داشتند. نتیجه‌گیری نهایی: نتایج این مطالعه نشان می‌دهد محیط I بیشترین تشابه با شرایط برون تنی را در مقایسه با محیط‌های II و III ایجاد نموده و سلول‌های نورونی بیشتر قادر به حفظ خصوصیات فیزیولوژیک خود در این محیط می‌باشند.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>163</FPAGE>
						<TPAGE>170</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>محمد حسین</Name>
						<MidName></MidName>		
						<Family>گرانمایه</Family>
						<NameE>Mohammad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Geranmayeh</FamilyE>
						<Organizations>
							<Organization>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mhgeranmayeh@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>علی</Name>
						<MidName></MidName>		
						<Family>باغبان زاده</Family>
						<NameE>Ali</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Baghbanzadeh</FamilyE>
						<Organizations>
							<Organization>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mhgeranmayeh@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>عباس</Name>
						<MidName></MidName>		
						<Family>برین</Family>
						<NameE>Abbas</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Barin</FamilyE>
						<Organizations>
							<Organization>Department of Microbiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>abarin05@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>جمیله</Name>
						<MidName></MidName>		
						<Family>سالار آملی</Family>
						<NameE>Jamileh</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Salar-Amoli</FamilyE>
						<Organizations>
							<Organization>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>jsalaramoli@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمد مهدی</Name>
						<MidName></MidName>		
						<Family>دهقان</Family>
						<NameE>Mohammad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Dehghan</FamilyE>
						<Organizations>
							<Organization>Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mdehghan@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>cortical neurons</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>isolation</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>primary cell culture</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>rat</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Barclay, D.C., Hallbergson, A.F., Montague, J.R., Mudd, L.M. (2005) Reversal of ethanol toxicity in embryonic neurons with growth factors and estrogen. Brain Res Bull. 67: 459-465.##Brewer, G.J., Torricelli, J.R. (2007) Isolation and culture of adult neurons and neurospheres. Nat Protoc. 2: 1490-1498.##Briz, V., Molina-Molina, J.M., Sánchez-Redondo, S., Fernández, M.F., Grimalt, J.O., Olea, N., Rodríguez-Farré, E., Suñol, C. (2011) Differential estrogenic effects of the persistent organochlorine pesticides dieldrin, endosulfan, and lindane in primary neuronal cultures. Toxicol Sci. 120: 413-427.##Chen, T., Fei, F., Jiang, X.F., Zhang, L., Qu, Y., Huo, K., Fei, Z. (2012) Down-regulation of Homer1b/c attenuates glutamate-mediated excitotoxicity through endoplasmic reticulum and mitochondria pathways in rat cortical neurons. Free Radic Biol Med. 52: 208-217.##Choi, D.W., Maulucci-Gedde, M., Kriegstein, A.R. (1987) Glutamate neurotoxicity in cortical cell culture. J Neurosci. 7: 357-368.##Dhandapani, K.M., Wade, F.M., Wakade, C., Mahesh, V.B., Brann, D.W. (2005) Neuroprotection by stem cell factor in rat cortical neurons involves AKT and NFκB. J Neurochem. 95: 9-19.##Harrill, J.A., Freudenrich, T.M., Machacek, D.W., Stice, S.L., Mundy, W.R. (2010) Quantitative assessment of neurite outgrowth in human embryonic stem cell-derived hN2™ cells using automated high-content image analysis. Neurotoxicology. 31: 277-290.##Harrill, J.A., Freudenrich, T.M., Robinette, B.L., Mundy, W.R. (2011) Comparative sensitivity of human and rat neural cultures to chemical-induced inhibition of neurite outgrowth. Toxicol Appl Pharmacol. 256: 268-280.##Harrill, J.A., Mundy, W.R. (2011) Quantitative assessment of neurite outgrowth in PC12 cells. Methods Mol Biol. 758: 331-348.##Harrill, J.A., Robinette, B.L., Freudenrich, T., Mundy, W.R. (2013) Use of high content image analyses to detect chemical-mediated effects on neurite sub-populations in primary rat cortical neurons. Neurotoxicology. 34: 61-73.##Hasan, M.R., Kim, J.H., Kim, Y.J., Kwon, K.J., Shin, C.Y., Kim, H.Y., Han, S.H., Choi, D.H., Lee, J. (2013) Effect of HDAC inhibitors on neuroprotection and neurite outgrowth in primary rat cortical neurons following ischemic insult. Neurochem Res. 38: 1921-1934.##Heber, S., Herms, J., Gajic, V., Hainfellner, J., Aguzzi, A., Rulicke, T., Kretzschmar, H., Von Koch, C., Sisodia, S., Tremml, P., Lipp, H.P., Wolfer, D.P., Muller, U. (2000) Mice with combined gene knock-outs reveal essential and partially redundant functions of amyloid precursor protein family members. J Neurosci. 20: 7951-7963.##Jeerage, K.M., Oreskovic, T.L., Hume, S.L. (2012) Neurite outgrowth and differentiation of rat cortex progenitor cells are sensitive to lithium chloride at non-cytotoxic exposures. Neurotoxicology. 33: 1170-1179.##Kim, H.J., Magrane, J. (2011) Isolation and culture of neurons and astrocytes from the mouse brain cortex. Methods Mol Biol. 793: 63-75.##Kim, J.Y., Jeong, H.Y., Lee, H.K., Kim, S., Hwang, B.Y., Bae, K., Seong, Y.H. (2012) Neuroprotection of the leaf and stem of Vitis amurensis and their active compounds against ischemic brain damage in rats and excitotoxicity in cultured neurons. Phytomedicine. 19: 150-159.##Koh -y J., Choi, D.W. (1988) Vulnerability of cultured cortical neurons to damage by excitotoxins: Differential susceptibility of neurons containing NADPH-diaphorase. J Neurosci. 8: 2153-2163.##Koo, K.A., Kim, S.H., Oh, T.H., Kim, Y.C. (2006) Acteoside and its aglycones protect primary cultures of rat cortical cells from glutamate-induced excitotoxicity. Life Sci. 79: 709-716.##Kuwagata, M. (2012) Current problems of in vivo developmental neurotoxicity tests and a new in vivo approach focusing on each step of the developing central nervous system. Congenit Anom. 52: 129-139.##Li, D., Gu, X., Lu, L., Liang, L. (2010) Effects of phenylalanine on the survival and neurite outgrowth of rat cortical neurons in primary cultures: Possible involvement of brain-derived neurotrophic factor. Mol Cell Biochem. 339: 1-7.##Li, L., Liu, Q.R., Xiong, X.X., Liu, J.M., Lai, X.J., Cheng, C., Pan, F., Chen, Y., Yu, S.B., Yu, A.C.H., Chen, X.Q. (2014) Neuroglobin promotes neurite outgrowth via differential binding to PTEN and Akt. Mol Neurobiol. 49: 149-162.##Liu, D., Bi, Y., Liu, Z., Liu, H., Li, Z. (2014) The expression of vesicular glutamate transporter 3 and vesicular monoamine transporter 2 induced by brain-derived neurotrophic factor in dorsal root ganglion neurons in vitro. Brain Res Bull. 100: 93-106.##Maekawa, F., Tsuboi, T., Oya, M., Aung, K.H., Tsukahara, S., Pellerin, L., Nohara, K. (2013) Effects of sodium arsenite on neurite outgrowth and glutamate AMPA receptor expression in mouse cortical neurons. Neurotoxicology. 37: 197-206.##Nabiuni, M., Rasouli, J., Parivar, K., Kochesfehani, H.M., Irian, S., Miyan, J.A. (2012) In vitro effects of fetal rat cerebrospinal fluid on viability and neuronal differentiation of PC12 cells. Fluids Barriers CNS. 9: 8.##Noshita, T., Murayama, N., Oka, T., Ogino, R., Nakamura, S., Inoue, T. (2012) Effect of bFGF on neuronal damage induced by sequential treatment of amyloid β and excitatory amino acid in vitro and in vivo. Eur J Pharmacol. 695: 76-82.##Pacifici, M., Peruzzi, F. (2012) Isolation and culture of rat embryonic neural cells: a quick protocol. J Vis Exp. JoVE. 63: e3965, doi:10.3791/3965.##Pinton, S., Souza, A. C., Sari, M.H.M., Ramalho, R.M., Rodriguesb, C.M.P., Nogueiraa, C.W. (2013) P,p’-Methoxyl-diphenyl diselenide protects against amyloid-β induced cytotoxicity in vitro and improves memory deficits in vivo. Behav Brain Res. 247: 241-247.##Radio, N.M., Freudenrich, T.M., Robinette, B.L., Crofton, K.M., Mundy, W.R. (2010) Comparison of PC12 and cerebellar granule cell cultures for evaluating neurite outgrowth using high content analysis. Neurotoxicol Teratol. 32: 25-35.##Wu, H., Mahmood, A., Qu, C., Xiong, Y., Chopp, M. (2012) Simvastatin attenuates axonal injury after experimental traumatic brain injury and promotes neurite outgrowth of primary cortical neurons. Brain Res. 1486: 121-130.##Xu, J., Xilouri, M., Bruban, J., Shioi, J., Shao, Z., Papazoglou, I., Vekrellis, K., Robakis, N.K. (2011) Extracellular progranulin protects cortical neurons from toxic insults by activating survival signaling. Neurobiol Aging. 32: 2326.e2325-2326.e2316.##Yan, T., Chopp, M., Ye, X., Liu, Z., Zacharek, A., Cui, Y., Roberts, C., Buller, B., Chen, J. (2012) Niaspan increases axonal remodeling after stroke in type 1 diabetes rats. Neurobiol Dis. 46: 157-164.##Yu, X., An, L. (2002) A serum- and antioxidant-free primary culture model of mouse cortical neurons for pharmacological screen and studies of neurotrophic and neuroprotective agents. Cell Mol Neurobiol. 22: 197-206.##Zeron, M.M., Hansson, O., Chen, N., Wellington, C.L., Leavitt, B.R., Brundin, P., Hayden, M.R., Raymond, L.A. (2002) Increased sensitivity to N-methyl-D-aspartate receptor-mediated excitotoxicity in a mouse model of Huntington’s disease. Neuron. 33: 849-860.##Zhang, J., Li, L., Chen, X., Zhang, B., Wang, Y., Yamamoto, K. (2000) Effects of a traditional Chinese medicine, Qing Nao Yi Zhi Fang, on glutamate excitotoxicity in rat fetal cerebral neuronal cells in primary culture. Neurosci Lett. 290: 21-24.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>مطالعه بر گلوکوز، انسولین، اسیدهای چرب غیر استریفیه، بتاهیدروکسی بوتیریک اسید و پروفایل چربی سرم در دورههای مختلف</TitleF>
				<TitleE>Study on serum glucose, insulin, NEFA, BHBA and lipid profile in different productive status of high producing Holstein dairy cows</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55285.html</URL>
                <DOI>10.22059/ijvm.2015.55285</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: Metabolic profiles have been used in efforts to predict pre parturient problems and fertility, to diagnose metabolic diseases, and to assess nutritional status in dairy cows. These profiles may help to confirm the diagnosis of sub clinical diseases, to be aware of possible causes of infertility in the herds, or to monitor improvement in herd animals. OBJECTIVES: This study investigated changes in the metabolic profile of high producing Holstein dairy cows from early lactation to close-up dry periods. The results of the current research can provide useful guidelines for management strategies during different physiological phases of high producing Holstein dairy cows. METHODS: Twenty-five multiparous high producing Holstein dairy cows were selected from a high producing industrial dairy farm. Cattle were divided into 5 equal groups of early, mid and late lactation and far-off and close-up dry cows. Blood samples were collected from all cows and sera were separated to evaluate glucose, insulin, β-hydroxybutyric acid (BHBA), non-esterified fatty acid (NEFA), cholesterol, triglyceride (TG), high, low and very low density lipoproteins (HDL-cholesterol, LDL-cholesterol and VLDL-cholesterol). RESULTS: The highest levels of insulin were detected in mid lactation and close-up dry periods. The changing patterns of BHBA and NEFA were significant and the highest levels of these biomarkers were detected in the early lactation group. The decreasing pattern of BHBA and NEFA were seen from early lactation to far-off dry cows. Significant elevations were seen in these biomarkers from far-off to close-up dry cows. CONCLUSIONS: The results of the present study show that metabolic biomarkers change in high producing Holstein dairy cows, under different physiological states. These changes are induced commonly by negative energy balance, lactogenesis and fetal growth in each state.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  پروفایل متابولیک به منظور پیش بینی مسائل حوالی زایمان و وضعیت باروری، تشخیص بیماریهای متابولیک و دستیابی به شرایط تغذیه‌ای در گاوهای شیری مورد استفاده قرار گرفته است. این پروفایل ممکن است در تأیید تشخیص بیماریهای تحت بالینی، آگاهی از عوامل محتمل ناباروری در گله‌ها یا بهبود نظارت بر حیوانات گله یاری رسان باشد. هدف: مطالعه حاضر به منظور دستیابی به تصویری از تغییرات پروفایل متابولیک در جریان گردش خون گاوهای هلشتاین شیری پرتولید از ابتدای شیردهی تا انتهای دوره خشکی و آبستنی طراحی شد. نتایج این مطالعه می‌تواند الگویی مفید در اتخاذ استراتژی‌های مدیریتی در خلال دوره‌های مختلف فیزیولوژیک گاوهای هلشتاین شیری پرتولید فراهم کند. روش کار: تعداد 25 رأس گاو هلشتاین شیری پرتولید چند شکم زاییده از یک واحد گاوداری شیری صنعتی پرتولید انتخاب شدند. گاوها به 5 گروه مساوی شامل ابتدا، میانه و انتهای شیرواری و ابتدا و انتهای خشکی تقسیم شدند. نمونه‌های خون از تمام گاوها اخذ شد و سرم‌ها به منظور ارزیابی گلوکوز، انسولین، بتا-هیدروکسی بوتیریک اسید (BHBA)، اسید‌های چرب غیر استریفیه (NEFA)، کلسترول، تری گلیسیرید (TG)، لیپوپروتئین‌ها با چگالی بالا، کم و بسیار کم (HDL، LDL و VLDL) جداسازی شدند. نتایج: بالاترین غلظت انسولین در گروه‌های میانه شیرواری و انتهای خشکی مشاهده شد. الگوی تغیرات BHBA و NEFA در خلال دوره‌های مختلف معنی‌دار بود و بیشترین غلظت این بیومارکرها در گروه ابتدای شیرواری تشخیص داده شد. الگوی کاهشی غلظت BHBA و NEFA از ابتدای شیرواری تا ابتدای خشکی مشاهده شد. افزایش این بیومارکرها از گاوهای ابتدای خشکی تا انتهای خشکی معنی‌دار بود. نتیجه‌گیری‌نهایی: نتایج مطالعه حاضر نشان داد که بیومارکرهای متابولیک در خلال دوره‌های مختلف فیزیولوژیک گاوهای هلشتاین شیری پرتولید تغییر می‌کند. این تغییرات عمدتا به واسطه توازن منفی انرژی، شیرواری و رشد جنین در هر دوره القا می‌شوند.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>171</FPAGE>
						<TPAGE>178</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>علی اصغر</Name>
						<MidName></MidName>		
						<Family>چالمه</Family>
						<NameE>Aliasghar</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Chalmeh</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>achalmeh81@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>مهرداد</Name>
						<MidName></MidName>		
						<Family>پورجعفر</Family>
						<NameE>Mehrdad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Pourjafar</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>dmp4m@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>سعید</Name>
						<MidName></MidName>		
						<Family>نظیفی</Family>
						<NameE>Saeed</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Nazifi</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>nazifi@shirazu.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>فروغ</Name>
						<MidName></MidName>		
						<Family>مومنی فر</Family>
						<NameE>Foroogh</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Momenifar</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>forooghmomenifar@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محبوبه</Name>
						<MidName></MidName>		
						<Family>محمدی</Family>
						<NameE>Mahboobeh</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Mohamadi</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mahgol000@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>changing pattern</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>lactogenesis</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>fetal growth</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Holstein dairy cows</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>metabolic profile</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Abell, L.L., Levy, B.B., Brodie, B.B., Kendall, F.E. (1952) A simplified method for the estimation of total cholesterol in serum and determination of its specificity. J Biol Chem. 195: 357-366.##Bell, A., Burhans, W.S., Overton, T.R. (2000) Protein nutrition in late pregnancy, maternal protein reserves and lactation performance in dairy cows. Proc Nutr Soc. 59: 119-126.##Bell, A.W. (1995) Regulation of organic nutrient metabolism during transition from late pregnancy to early lactation. J Anim Sci. 73: 2804-2819.##Bickerstaffe, R., Annison, E.F., Linzell, J.L. (1974) The metabolism of glucose, acetate, lipids and amino acids in lactating dairy cows. J Agric Sci. 82: 71-85.##Bossaert, P., Leroy, J.L., De Campeneere, S., De Vliegher, S., Opsomer, G. (2009) Differences in the glucose induced insulin response and the peripheral insulin responsiveness between neonatal calves of the Belgian Blue, Holstein-Friesian, and East Flemish breeds. J Dairy Sci. 92: 4404-4011.##Burtis, C.A., Ashwood, E.R. (1994) Tietz Textbook of Clinical Chemistry. (2nd ed.) W.B. Saunders Co, Philadelphia, USA.##Debras, E., orizard, J., Aina, E., Tesseraud, S., Qlampredon, C., Amal, M. (1989) Insulin sensitivity and responsiveness during lactation and dry period in goats. Am J Physiol. 256: E295-302.##De Koster, J.D., Opsomer, G. (2013) Insulin resistance in dairy cows. Vet Clin North Am Food Anim Pract. 29: 299-322.##Douglas, G.N., Overton, T.R., Bateman, H.G., Drackley, J.K. (2004) Peripartal metabolism and production of Holstein cows fed diets supplemented with fat during the dry period. J Dairy Sci. 87: 4210-4220.##Emery, R.S., Liesman, J.S., Herdt, T.H. (1992) Metabolism of long chain fatty acids by ruminant liver. J Nutr. 122: 832-837.##Faulkner, A., Pollock, H.T. (1990) Metabolic responses to euglycaemic hyperinsulinaemia in lactating and non-lactating sheep in vivo. J Endocrinol. 124: 59-66.##Fiore, E., Gianesella, M., Arfuso, F., Giudice, E., Piccione, G., Lora, M., Stefani, A., Morgante, M. (2014) Glucose infusion response on some metabolic parameters in dairy cows during transition period. Arch Tierz. 57: 1-9.##Friedewald, W.T., Levy, R.I., Fredrickson, D.S. (1972) Estimation of the concentration of low density lipoprotein cholesterol without the use of the preparative ultra centrifuge. Clin Chem. 18: 499-502.##Ghanem, M.M., Mahmoud, M.E., Abd El-Raof, Y.M., El-Attar, H.M. (2012) Metabolic profile test for monitoring the clinical, haematological and biochemical alterations in cattle during peri-parturient period. Banha Vet Med J. 23: 13-23.##Graulet, B., Gruffat, D., Durand, D., Bauchart, D. (1998) Fatty acid metabolism and very low density lipoprotein secretion in liver slices from rats and preruminant calves. J Biochem. 124: 1212-1219.##Grum, D.E., Drackley, J.K., Younker, R.S., LaCount, D.W., Veenhuizen, J.J. (1996) Nutrition during the dry period and hepatic lipid metabolism of periparturient dairy cows. J Dairy Sci. 79: 1850-1864.##Grummer, R.R., Mashek, D.G., Hayirli, A. (2004) Dry matter intake and energy balance in the transition period. Vet Clin North Am Food Anim Pract. 20: 447-470.##Hawagane, S.D., Shinde, S.B., Rajguru, D.N. (2009) Haematological and blood biochemical profile in lactating buffaloes in and around Parbhani city. Vet World. 2: 467-469.##Herdt, T.H. (2000) Variability characteristics and test selection in herd-level nutritional metabolic profile testing. Vet Clin North Am Food Anim Pract. 16: 387-403.##Kahn, C.R. (1978) Insulin resistance, insulin insensitivity, and insulin unresponsiveness: a necessary distinction. Metabolism. 12: 1893-1902.##Krajnicakova, M., Kovac, G., Kostecky, M., Valocky, I., Maracek, I., Sutiakova, I., Lenhardt, L. (2003) Selected clinic-biochemical parameters in the puerperal period of goats. Bull Vet Inst Pulawy. 47: 177-182.##Lewis, G.F., Carpentier, A., Adeli, K., Giacca, A. (2002) Disordered fat storage and mobilization in the pathogenesis of insulin resistance and type 2 diabetes. Endocr Rev. 23: 201-229.##McGowan, M.W., Artiss, J.D., Strandbergh, D.R., Zak, B. (1983) A peroxidase coupled method for the colorimetric determination of serum triglycerides. Clin Chem. 29: 538-542.##McNamara, J.P. (1991) Regulation of adipose tissue metabolism in support of lactation. J Dairy Sci. 74: 706-719.##Piccione, G., Messina, V., Marafioti, S., Casella, S., Giannetto, C., Fazio, F. (2012) Changes of some haematochemical parameters in dairy cows during late gestation, post partum, lactation and dry periods. Vet Med Zoot. 58: 59-64.##Pires, J.A.A., Souza, A.H., Grummer, R.R. (2007) Induction of hyperlipidemia by intravenous infusion of tallow emulsion causes insulin resistance in Holstein cows. J Dairy Sci. 90: 2735-2744.##Pullen, D.L., Palmquist, D.L., Emery, R.S. (1989) Effect on days of lactation and methionine hydroxy analog on incorporation of plasma fatty acids into plasma triglycerides. J Dairy Sci. 72: 49-58.##Roche, J. R., Frggens, N.C., Kay, J.K., Fisher, M.W., Stafford, K.J., Berry, D.P. (2009) Invited review: Body condition score and its association with dairy cow productivity, health and welfare. J Dairy Sci. 92: 5769-5801.##Rukkwamsuk, T., Wensing, T., Geelen, M.J. (1999) Effect of overfeeding during the dry period on the rate of esterification in adipose tissue of dairy cows during the periparturient period. J Dairy Sci. 82: 1164-1169.##Sartin, J.L., Cummins, K.A., Kemppainen, R.J., Marple, D.N., Rahe, C.H., Williams, I.C. (1985) Glucagon, insulin, and growth hormone responses to glucose infusion in lactating dairy cows. Am J Physiol. 248: E108-114.##Sartin, J.L., Kemppaben, R.J., Cllmminn, K.A., Williams, J.C. (1988) Plasma concentrations of metabolic hormones in high and low producing dairy cows. J Dairy Sci. 71: 650-657.##Tanaka, M., Kamiya, Y., Suzuki, T., Nakai, Y. (2011) Changes in oxidative status in periparturient dairy cows in hot conditions. Anim Sci J. 82: 320-324.##Tanritanir, P., Dede, S., Ceylan, E. (2009) Changes in some macro minerals and biochemical parameters in female healthy siirt hair goats before and after parturition. J Anim Vet Adv. 8: 530-533.##Wathes, D.C., Cheng, Z., Chowdhury, W., Fenwick, M.A., Fitzpatrick, R., Morris, D.G., Patton, J., Murphy, J.J. (2009) Negative energy balance alters global gene expression and immune responses in the uterus of postpartum dairy cows. Physiol Genomics. 39: 1-13.##Wilson, S., MacRae, J.C., Buttay, P.J. (1983) Glucose production and utilization in non-pregnant, pregnant and lactating ewes. Br J Nutr. 50: 303-316.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>تأثیر سه عصاره گیاه دارویی آویشن، سیر و زیره سیاه بر فراسنجه های خونی، عملکرد تولید، کیفیت تخم، قدرت جوجه درآوری</TitleF>
				<TitleE>Effect of thyme, garlic and caraway herbal extracts on blood parameters, productivity, egg quality, hatchability and intestinal bacterial population of laying Japanese quail</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55286.html</URL>
                <DOI>10.22059/ijvm.2015.55286</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: In the current Iranian poultry industry, antibiotics are the most frequently used additive in poultry feeds to increase productivity. The negative effects on human health, resulting from the consumption of chicken whose feeds contain antibiotics, makes finding an appropriate alternative of great importance. As a result of their nature, herbal extracts could be specifically considered for this purpose. OBJECTIVES: This study aimed to find an appropriate and harmless feed additive to increase the quality and quantity of poultry eggs. METHODS: A completely randomized design including 4 treatments, 4 replications and 4 birds in each experimental unit was applied. Herbal extracts were added to drinking water of treatments in ratio of 1:1000, with the control group containing no additives in their water. The number and weight of produced eggs were measured on a daily basis, feed consumption on weekly basis and the egg quality, yolk cholesterol, hatchability and intestinal bacterial population were measured at the end of experiment after 8 weeks. RESULTS: Herbal extract treatments showed no overall effect on quality and quantity of produced eggs in comparison with control; however, the thyme and garlic extracts reduced the cholesterol of serum and yolk relative to the control. Herbal extracts did not significantly affect the hatchability of fertile eggs. The herbal extracts caused a significant decrease in the intestinal bacterial population of laying quails. CONCLUSIONS: The garlic extract had the most decreasing effect on the cholesterol of serum and egg yolk. Furthermore, thyme extract had the most decreasing effect on the intestinal bacterial population.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  در حال حاضر در صنعت دام و طیور کشور، آنتی‌بیوتیک‌ها به عنوان پرکاربردترین افزودنی به منظور افزایش تولید در خوراک دام و طیور به کار می‌روند که با توجه به اثرات سوء ایجادشده در انسان از مصرف محصولات دامی که در تغذیه آنها از آنتی‌بیوتیک استفاده شده است، یافتن یک جایگزین مناسب برای آنها از اهمیت ویژه‌ای برخوردار بوده که در این میان گیاهان دارویی به دلیل ماهیتشان می‌توانند به طور ویژه‌ای مورد توجه قرار گیرند. هدف: هدف از این مطالعه یافتن یک افزودنی غذایی مناسب و بی‌ضرر برای افزایش کمیت و کیفیت تخم‌های تولیدی در طیور تخم‌گذار است. روش کار: از طرحی کاملاً تصادفی با 4 تیمار، 4 تکرار و 4 پرنده در هر واحد آزمایشی استفاده شد. عصاره‌های گیاهان دارویی به نسبت 1 به 1000 به آب آشامیدنی تیمارهای مربوطه اضافه گشت و آب آشامیدنی گروه شاهد بدون هیچ افزودنی در اختیار پرندگان قرار گرفت. مقدار و وزن تخم‌های تولیدی به صورت روزانه، مصرف خوراک به صورت هفتگی و کیفیت تخم‌های تولیدی و کلسترول زرده و قدرت جوجه درآوری و جمعیت باکتریایی روده در انتهای دوره‌ آزمایشی بعد از هشت هفته اندازه‌گیری شد. نتایج:  تیمارهای گیاهان دارویی به طور کلی تأثیری بر کمیت و کیفیت تخم‌های تولیدی نسبت به تیمار شاهد نداشتند، ولی عصاره آویشن و سیر باعث کاهش کلسترول سرم و زرده در مقایسه با تیمار شاهد شدند. همچنین عصاره‌های گیاهان دارویی تأثیر معنی‌داری بر درصد جوجه درآوری بلدرچین‌های مولد نداشتند. گیاهان دارویی به طور معنی‌داری باعث کاهش جمعیت باکتریایی روده‌های بلدرچین‌های مولد شدند. نتیجه گیری نهایی: عصاره گیاه دارویی سیر باعث بیشترین اثر کاهشی بر کلسترول سرم بلدرچین‌ها و زرده تخم‌های تولیدی و عصاره گیاه دارویی آویشن باعث بیشترین اثر کاهشی جمعیت باکتریایی شدند.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>179</FPAGE>
						<TPAGE>187</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>علی رضا</Name>
						<MidName></MidName>		
						<Family>بهنامی فر</Family>
						<NameE>Alireza</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Behnamifar</FamilyE>
						<Organizations>
							<Organization>Department of Poultry Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran–Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>behnamialireza@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>شعبان</Name>
						<MidName></MidName>		
						<Family>رحیمی</Family>
						<NameE>Shaban</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Rahimi</FamilyE>
						<Organizations>
							<Organization>Department of Poultry Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran–Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>rahimi_s80@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمد امیر</Name>
						<MidName></MidName>		
						<Family>کریمی ترشیزی</Family>
						<NameE>Mohammad Amir</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Karimi Torshizi</FamilyE>
						<Organizations>
							<Organization>Department of Poultry Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran–Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>karimitm@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>سعید</Name>
						<MidName></MidName>		
						<Family>حسن پور</Family>
						<NameE>Saeed</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Hasanpor</FamilyE>
						<Organizations>
							<Organization>Department of Poultry Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran–Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>s.hasanpoor@modares.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>زهرا</Name>
						<MidName></MidName>		
						<Family>محمدزاده</Family>
						<NameE>Zahra</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Mohamadzade</FamilyE>
						<Organizations>
							<Organization>Department of Poultry Sciences, Faculty of Agriculture, Tarbiat Modares University, Tehran–Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mohamadzadez@ymail.com</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Blood parameters</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>eggs quality and quantity</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>herbal extracts</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Japanese quail</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Adler, A. J., Holub, B. J. (1997) Effect of garlic and fish-oil supplementation on serum lipid and lipoprotein concentrations in hypercholesterolemic men. Am J Clin Nutr. 65: 445-450.##Al-Kassi, G.A. (2010) Effect of feeding cumin (Cuminum cyminum) on the performance and some blood traits of broiler chicks. Pak J Nutr. 9: 72-75.##Amagase, H., Petesch, B.L., Matsuura, H., Kasuga, S., Itakura, Y. (2001) Intake of garlic and it’s bioactive components. J Nutr. 131: 955-962.##Awad, W.A., Ghareeb, K., Abdel-Raheem, S., Bohm, J. (2009) Effects of dietary inclusion of probiotic and synbiotic on growth performance, organ weights, and intestinal histomorphology of broiler chickens. Poult Sci. 88: 49-55.##Berthold, H.K., Sudhop, T., Von Bergmann, K. (1998) Effect of a garlic oil preparation on serum lipoproteins and cholesterol metabolism: a randomized controlled trial. JAMA. 279: 1900-1902.##Botsoglou, N.A., Florou-Paneri, P., Christaki, E., Fletouris, D.J., Spais, A.B. (2002) Effect of dietary oregano essential oil on performance of chickens and on iron-induced lipid oxidation of breast, thigh and abdominal fat tissues. Br Poult Sci. 43: 223-230.##Case, G.L., He, L., Mo, H., Elson, C.E. (1995) Induction of geranyl pyrophosphatase activity by cholesterol suppressive isoprenoids. Lipids. 30: 357-359.##Cross, D.E., McDevitt, R.M., Hillman, K., Acamovic, T. (2007) The effect of herbs and their associated essential oils on performance, dietary digestibility and gut microflora in chickens from 7 to 28 days of age. Br Poult Sci. 48: 496-506.##Crowell, P.L. (1999) Prevention and therapy of cancer by dietary monoterpenes. J Nutr. 129: 775-778.##Dorman, H.J.D., Deans, S.G. (2000) Antimicrobial agents from plants: antibacterial activity of plant volatile oils. J Appl Microbiol. 88: 308-316.##Er, D., Wang, Z., Cao, J., Chen, Y. (2007) Effect of monochromatic light on the egg quality of laying hens. J Appl Poult Res. 16: 605-612.##Fitch, M.E., Mangels, A.R., Altmann, W.A., El Hawary, M., Qureshi, A.A., Elson, C.E. (1989) Microbiological screening of mevalonate-suppressive minor plant constituents. J Agric Food Chem. 37: 687-691.##Gachkar, L., Yadegari, D., Rezaei, M.B., Taghizadeh, M., Astaneh, S.A., Rasooli, I. (2007) Chemical and biological characteristics of Cuminum cyminum and Rosmarinus officinalis essential oils. Food Chem. 102: 898-904.##Gholipoor, V., Shahryar, H.A., Ebrahimnezhad, Y. (2013) Effects of Oregano and Thyme on hatchability of stored eggs of Japanese quail. Adv Biores. 4: 85-88.##Hammer, K.A., Carson, C.F., Riley, T.V. (1999) Antimicrobial activity of essential oils and other plant extracts. J Appl Microbiol. 86: 985-990.##Helander, I.M., Alakomi, H.L., Latva-Kala, K., Mattila-Sandholm, T., Pol, I., Smid, E.J., Gorris, L.G.M., Von Wright, A. (1998) Characterization of the action of selected essential oil components on Gram-negative bacteria. J Agric Food Chem. 46: 3590-3595.##Isaacsohn, J.L., Moser, M., Stein, E.A., Dudley, K., Davey, A., Liskov, E., Black, H.R. (1998) Garlic powder and plasma lipids and lipoproteins: A multicenter, randomized, placebo controlled trial. Arch Intern Med. 158: 1189-1194.##Kamel, C., Garnsworthy, P.C., Wiseman, J. (2001) Tracing modes of action and the roles of plant extracts in non-ruminants. Recent Adv Anim Nutr. 2001: 135-150.##Khajeali, Y., Kheiri, F., Rahimian, Y., Faghani, M. (2013) Effect of use different levels of Caraway (Carum carvi L) Powder on Performance, some blood parameters and intestinal morphology on broiler chicks. World Appl Sci J. 19: 1202-1207.##Khan, S.H., Hasan, S., Sardar, R., Anjum, M. A. (2008) Effects of dietary garlic powder on cholesterol concentration in Native Desi laying hens. Am J Food Technol. 3: 207-213.##Lee, K.W., Everts, H., Beynen, A.C. (2004) Essential oils in broiler nutrition. Int J Poult Sci. 3: 738-752.##Liu, L., Yeh, Y.Y. (2000) In hibition of cholesterol biosynthesis by organosulfur compounds derived from garlic. Lipids. 35: 197-203.##Losa, R. (2001) The use of essential oils in animal nutrition. Cahiers OM. 54: 39-44.##Middleton, B., Kok-Pheng, H. (1982) Inhibition of hepatic 3-hydroxy-3-methylglutaryl-CoA reductase and in vivo rates of lipogenesis by a mixture of pure cyclic monoterpenes. Biochem Pharmacol. 31: 2897-2901.##Mitsch, P., Zitterl-Eglseer, K., Köhler, B., Gabler, C., Losa, R., Zimpernik, I. (2004) The effect of two different blends of essential oil components on the proliferation of Clostridium perfringens in the intestines of broiler chickens. Poult Sci. 83: 669-675.##Mottaghitalab, M., Taraz, Z. (2002) Effects of garlic powder (Allium sativum) on egg yolk and blood serum cholesterol in Aryan breed laying hens. Br Poult Sci. 43: 42-43.##Nelson, R.R. (1997) In vitro activities of five plant essential oils against methicillin-resistant Staphlococcus aureus and vancomycin-resistant Enterococcus faecium. J Antimicrob Chemother. 40: 305-306.##Papageorgiou, G., Botsoglou, N., Govaris, A., Giannenas, I., Iliadis, S., Botsoglou, E. (2003) Effect of dietary oregano oil and α‐tocopheryl acetate supplementation on iron‐induced lipid oxidation of turkey breast, thigh, liver and heart tissues. J Anim Physiol Anim Nutr. 87: 324-335.##Pasin, G., Smith, G.M.O., Mahony, M.O. (1998) Rapid determination of totalcholestrol in egg  yolk using commercial diagnostic cholesterol reagent. Food Chem. 61: 255- 259.##Reddy, R.V., Lightsey, S.F., Maurice, D.V. (1991) Effect of feeding garlic oil on performance and egg yolk cholesterol concentration. Poult Sci. 70: 2006-2009.##Silagy, C., Neil, A. (1994) Garlic as a lipid lowering agent. A meta-analysis. J R Coll Physicians Lond. 28: 39-45.##Sklan, D., Berner, Y.N., Rabinowitch, H.D. (1992) The effect of dietary onion and garlic on hepatic lipid concentrations and activity of antioxidative enzymes in chicks. J Nutr Biochem. 3: 322-325.##Van Den Brand, H., Parmentier, H.K., Kemp, B. (2004) Effects of housing system (outdoor vs. cages) and age of laying hens on egg characteristics. Br Poult Sci. 45: 745-752.##Warshafsky, S., Kamer, R.S., Sivak, S.L. (1993) Effect of garlic on total serum cholesterol. A meta-analysis. Ann Intern Med. 119: 599-605.##Yalçın, S., Onbaşılar, E. E., Reisli, Z., Yalcın, S. (2006) Effect of garlic powder on the performance, egg traits and blood parameters of laying hens. J Sci Food Agric. 86: 1336-1339.##Youn, H.J., Noh, J.W. (2001) Screening of the anticoccidial effects of herb extracts against Eimeria tenella. Vet Parasitol. 96: 257-263.##Yu, S.G., Abuirmeileh, N.M., Qureshi, A.A., Elson, C.E. (1994) Dietary. beta.-ionone suppresses hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase activity. J Agric Food Chem. 42: 1493-1496.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>پارامترهای عملکرد پرورشی طیور در کوکسیدیوز تجربی درمان شده با دیکلازوریل و کلوپیدول، نیاز به ارزیابی منابع جدید</TitleF>
				<TitleE>Growth performance parameters in chicken experimental coccidiosis treated with Diclazuril and Clopidol: The need for assessing new anticoccidial resources</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55287.html</URL>
                <DOI>10.22059/ijvm.2015.55287</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: Coccidiosis is recognized as the parasitic disease that has the greatest economic impact on poultry production. Modern poultry production is largely dependent upon anticoccidials. Objectives: The aim of the present study was to determine and compare the efficacy of two chemical anticoccidials (Clopidol and Diclazuril) on oocyst shedding and their probable effects on growth performance and feed efficiency of broilers in experimental coccidiosis. Methods: One hundred and twenty Ross 308 one day old broilers were randomly assigned into 4 groups: CON+, infected with Eimeria mixed oocysts but not medicated; CON-, not infected and not medicated; CLO, infected and medicated with Clopidol; DIC, infected and medicated with Diclazuril. Chickens in all groups except negative control were inoculated by mixed sporulated oocysts of pathogenic Eimeria at the end of the 3rd week of age. Oocyst shedding was counted using a Mc Master counting chamber. Body weights, body weight gains, and feed conversion ratio were determined on weekly basis. Results: Obtained results showed that Diclazuril was more effective in reducing oocyst shedding than Clopidol. As expected, mean body weight in the positive control group was lower than other groups. But surprisingly, no significant difference was found between Diclazuril or Clopidol treated birds and positive control group, at the end of the experiment. In comparison of weight gain in different treatment groups except for the 4 and 5th week, no significant difference was found in different groups. In the last week of the experiment, difference in weight gain between groups was not significant. According to feed conversion ratio (FCR)  results, anticoccidial supplementation did not have any significant effect on improving FCR. ConclusionS: It is reported that some anticoccidials reduce feed consumption and feed conversion. It seems that neither of the present synthetic anticoccidials is completely satisfactory in controlling coccidiosis economic losses and new strategies are urgently required. </CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه: کوکسیدیوز به عنوان یک بیماری انگلی که بیشترین تأثیر اقتصادی را بر تولید طیور دارد، شناخته شده است. صنعت مدرن پرورش طیور به میزان زیادی وابسته به ترکیبات ضد کوکسیدیوز است. هدف: مطالعه حاضر جهت تعیین و مقایسه کارایی دو ضد کوکسیدیوز شیمیایی (کلوپیدول و دیکلازوریل) بر دفع اووسیست و همچنین اثرات احتمالی آنها بر عملکرد پرورشی و کارایی تغذیه‌ای طیور گوشتی در کوکسیدیوز تجربی انجام شده است. روش کار: تعداد 120 قطعه جوجه یک روزه نژاد Ross 308 بطور تصادفی گروه‌بندی شدند: کنترل مثبت؛ آلوده به کوکسیدیوز بدون درمان، گروه کنترل منفی؛ بدون آلودگی و بدون درمان، گروه  CLO؛ آلوده و درمان شده باکلوپیدول، گروه DIC؛ آلوده و درمان شده با دیکلازوریل. برای ایجاد کوکسیدیوز تمامی گروه‌ها بجز کنترل منفی با اووسیست اسپوروله عفونی در انتهای هفته سوم تلقیح شدند. میزان دفع اووسیست با استفاده از لام مک مستر شمارش گردید. وزن بدن، وزنگیری و ضریب تبدیل غذایی هر هفته اندازه‌گیری و محاسبه گردید. نتایج: شمارش اووسیست نشان داد که دیکلازوریل در کاهش تعداد اووسیست کارآمدتر از کلوپیدول بود. میانگین وزن بدن در گروه کنترل مثبت از سایر گروه‌ها پایین‌تر بود. ولی در انتهای مطالعه میانگین وزن در گروه‌های درمان شده با کلوپیدول و دیکلازوریل با گروه کنترل مثبت تفاوت معنی‌داری را نشان نداد. در مقایسه وزنگیری میان گروه‌های مختلف بجز در هفته چهارم و پنجم در سایر هفته‌ها تفاوت معنی‌داری مشاهده نشد. بر پایه نتایج بدست آمده از FCR اضافه نمودن ترکیبات آنتی کوکسیدیال اثر معنی‌داری بر بهبود آن نداشت. نتیجه‌گیری‌نهایی: گزارش شده است که برخی از ترکیبات ضدکوکسیدیوز منجر به کاهش مصرف خوراک و ضریب تبدیل غذایی می‌شوند. به نظر می‌رسد هیچکدام از ضدکوکسیدیوزهای شیمیایی مورد استفاده در مطالعه حاضر در کنترل زیان‌های اقتصادی کوکسیدیوز به طور کامل مؤثر نمی‌باشند و ارائه استراتژی‌های جدید مورد نیاز می‌باشد.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>189</FPAGE>
						<TPAGE>194</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>حامد</Name>
						<MidName></MidName>		
						<Family>اسدی ایرائی</Family>
						<NameE>Hamed</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Asadi Iraee</FamilyE>
						<Organizations>
							<Organization>DVM, Private Veterinarian Practitioner, Amol, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>hasadi@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمد</Name>
						<MidName></MidName>		
						<Family>اسدی ایرایی</Family>
						<NameE>Mohammad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Asadi Iraee</FamilyE>
						<Organizations>
							<Organization>Young Researchers Club, Islamic Azad University, Babol Branch, Babol, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>mohamadasadi@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محمدرضا</Name>
						<MidName></MidName>		
						<Family>یوسفی</Family>
						<NameE>Mohammad Reza</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Youssefi</FamilyE>
						<Organizations>
							<Organization>Department of Veterinary Parasitology, Faculty of Veterinary Medicine, Islamic Azad University, Babol Branch, Babol, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>youssefi929@hotmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>محدثه</Name>
						<MidName></MidName>		
						<Family>ابوحسینی طبری</Family>
						<NameE>Mohaddeseh</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Abouhosseini Tabari</FamilyE>
						<Organizations>
							<Organization>Faculty of Veterinary Medicine, Amol University of Special Modern Technologies, Amol, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>m_abuhoseini@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>coccidiosis</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Diclazuril</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Clopidol</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>growth performance</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Broilers</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Allen, P.C., Fetterer, R.H. (2002) Recent advances in biology and immunobiology of Eimeria species and in diagnosis and control of infection with these coccidian parasites of poultry. Clin Microbiol Rev. 15: 58-65.##Abbas, R.Z., Iqbal, Z., Khan, M.N., Hashmi, N., Hussain, A. (2009) Prophylactic efficacy of diclazuril in broilers experimentally infected with three field isolates of Eimeria tenella. Int J Agric Biol. 11: 606-610.##Arabkhazaeli, F., Modrisanei, M., Nabian, S., Mansoori, B., Madani, A. (2013) Evaluating the resistance of Eimeria spp. field isolates to anticoccidial drugs using three different indices. Iran J Parasitol. 8: 234-241.##Bahadoran, S., Hassanpour, H., Pirali kheirabadi, K., Shekarchian, S. (2014) Effect of clopidol and amprolium/ethopabate on performance and intestinal morphology of chickens with experimental coccidiosis. Kafkas Univ Vet Fak Derg. 20: 571-576.##Bell, D.D., Weaver, D.W. (2002) Commercial chicken meat and egg production, Kluwer Academic Publishers, Norwell, MA, The Netherlands.##Conway, D.P., Mathis, G.F., Johnson, J., Schwartz, M., Baldwin, C. (2001) Efficacy of diclazuril in comparison with chemical and ionophorous anticoccidials against Eimeria spp. in broiler chickens in floor pens. Poult Sci. 80: 426-430.##Lillehoj, H.S., Hong, Y., Kim, C. (2010) Quantitative genetic and functional genomics approaches to investigating parasite disease resistance and protective immune mechanisms in avian coccidiosis. Genomics for Animal Health. Dev Biol (Basel). Basel, Karger. 132: 67–75.##Mathis, F.G. (2001)  New organic anticoccidial can safely be used in feed. World Poultry. 17: 50-52.##Peeters, J.E., Derijcke, J., Verlinden, M., Wyffels, R. (1994) Sensitivity of avian Eimeria spp. to seven chemical and five ionophore anticoccidials in five Belgian integrated broiler operations. Avian Dis. 38: 483-493.##Pirali-kheirabadi, K., Zamani-Moghadam, A., Abdi, F., Bahonar, A.R. (2008) The effect of administration of anti-coccidial drugs on oocyst shedding and performance in experimental coccidiosis in broiler chickens. Int  J Vet Res 2: 67-73.##Rahbari, S., Mehrabani, M., Hesami, A. (1995) Resistance development of field isolated Eimeria SPP. against some anticoccidial drugs. J Vet Res (University of  Tehran). 50: 45-51.##Vancraeynest, D., De Gussem, M., Marien, M.,  Maertens, L. (2010) The anticoccidial efficacy of robenidine hydrochloride in Eimeria challenged rabbits. World Rabbit Sci. 18: 65-75.##Williams, R.B. (2006) Tracing the emergence of drug-resistance in coccidia Eimeria spp. of commercial broiler flocks medicated with decoquinate for the first time in the United Kingdom. Vet parasitol. 135: 1-14.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>-</TitleF>
				<TitleE>Comparison of broiler performance, blood biochemistry, hematology and immune response when feed diets were supplemented with ginger essential oils or mannan-oligosaccharide</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55288.html</URL>
                <DOI>10.22059/ijvm.2015.55288</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: Nutritional strategies targeting improvement of poultry performance and disease prevention are currently being developed and in this respect the dietary intake of spiced essential oils and pre-biotics in raising broilers is receiving attention. OBJECTIVES: This study was conducted to compare the effects of diet containing ginger essential oils (GEO) and mannan-oligosaccharide (MOS) on growth performance,  biochemical and hematological parameters, lymphoid organ weights and antibody response of broilers. METHODS: A total of 375 day old male broiler chicks were randomly assigned to five treatments (five replicates per treatment). Dietary treatments included basal diet as control, GEO-supplemented diets with inclusion levels of 50 (GEO1), 100 (GEO2) or 200 (GEO3) mg/kg, and MOS supplemented diet with an inclusion level of 2 g/kg. RESULTS: The birds fed on MOS and GEO3 diets exhibited better feed conversion ratio and higher body weight gain from 1 to 42 day of age compared with control birds (p&lt;0.05). Serum low density lipoprotein cholesterol level in the MOS, GEO2 or GEO3 groups was lower than that of the control group (p&lt;0.05). Serum cholesterol level was also lower in the GEO2 and MOS groups (p&lt;0.05). Feeding on GEO3 and MOS diets significantly increased relative bursa weight and secondary antibody titer against infectious bursal disease (IBD) and infectious bronchitis (IB) vaccines as compared with control diet (p&lt;0.05). CONCLUSIONS: The results showed that higher level of GEO (200 g/kg) similar to MOS supplementation, improved feed efficiency and immune response. This could meet consumers’ demand for a safe feed additive.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  استراتژی‌های تغذیه‌ای با هدف بهبود عملکرد طیور و پیشگیری از بیماریها در حال حاضر رو به توسعه است و در این راستا استفاده از مکمل‌های سودمند مانند اسانس ادویه‌ها یا پربیوتیک‌ها در پرورش جوجه‌های گوشتی مورد توجه قرار گرفته است. هدف: این مطالعه به منظور مقایسه اثرات جیره‌های غذایی حاوی اسانس زنجبیل (GEO) و مانان-الیگوساکارید (MOS) بر عملکرد رشد، پارامترهای بیوشیمیایی و هماتولوژی خون، وزن اندام‌های لنفاوی و پاسخ آنتی بادی در جوجه‌های گوشتی انجام شد. روش کار: در مجموع 375 قطعه جوجه گوشتی نر یک روزه به طور تصادفی به پنج تیمار (پنج تکرار در هر تیمار) تخصیص یافتند. جیره‌های غذایی شامل جیره پایه به عنوان شاهد، جیره‌های غذایی مکمل شده با GEO در سطوح mg/kg 50 (GEO1)، mg/kg‌100 (GEO2) و mg/kg 200 (GEO3)، و جیره غذایی مکمل شده با MOS در سطح g/kg‌2 بود. نتایج: پرنده‌های تغذیه شده با جیره‌های GEO3 و MOS ضریب تبدیل غذایی بهتر و افزایش وزن بدن بالاتری از 1 تا 42 روزگی در مقایسه با گروه شاهد نشان دادند (05/0&gt;p). سطح کلسترول لیپوپروتئین با چگالی کم سرم در گروه‌های GEO2، GEO3 و MOS کمتر از گروه شاهد بود (05/0&gt;‌p). سطح کلسترول سرم نیز در گروه‌های GEO2 و MOS کمتر بود (05/0&gt;‌p). تغذیه جیره‌های GEO3 و MOS به طور معنی‌داری وزن نسبی بورس و تیتر ثانویه آنتی بادی در برابر واکسن‌های بیماری بورس عفونی (IBD) و برونشیت عفونی (IB) را در مقایسه با جیره شاهد افزایش داد (05/0&gt;p). نتیجه‌گیری نهایی: نتایج نشان داد که سطح بالاتر GEOر(g/kg‌200)، شبیه به مکمل MOS، بازده خوراک و پاسخ ایمنی را بهبود بخشید. این می‌تواند تقاضای مصرف‌کننده‌ها برای افزودنی‌های خوراک بی خطر را تأمین کند.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
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						<FPAGE>195</FPAGE>
						<TPAGE>205</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>حسینعلی</Name>
						<MidName></MidName>		
						<Family>قاسمی</Family>
						<NameE>Hossein Ali</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Ghasemi</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, Faculty of Agriculture and Natural Resources, Arak University, Arak, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>haghasemi89@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>کامران</Name>
						<MidName></MidName>		
						<Family>طاهرپور</Family>
						<NameE>Kamran</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Taherpour</FamilyE>
						<Organizations>
							<Organization>Department of Animal Sciences, Faculty of Agriculture, Ilam University, Ilam, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>k.taherpour@ilam.ac.ir</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>ginger essential oils</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Prebiotic</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>performance</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>immune response</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Broilers</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Ali, B.H., Blunden, G., Tanira, M.O., Nemmar, A. (2008) Some phytochemical, pharmacological and toxicological properties of ginger (Zingiber officinale Roscoe): A review of recent research. Food Chem Toxicol. 46: 409-420.##Al-Saleh, I.A., Billedo, G., Inam, I.E. (2006) Level of selenium, DL-α-tocopgerol, DL-γ-tocopherol, all trans retinol, thymoquinone and thymol in different brands of Nigella sativa seeds. J Food Comp Anal. 19: 167-175.##Arslan, S.O., Gelir, E., Armutcu, F., Coskun, O., Gurel, A., Sayan, H., Celik, I.L. (2005) The protective effect of thymoquinone on ethanol-induced acute gastric damage in the rat. Nutr Res. 25: 673-680.##Azhir, D., Zakeri, A., Kargare-Rezapour, A. (2012) Effect of ginger powder rhizome on homural immunity of broiler chickens. Eur J Exp Biol. 2: 2090-2092.##Barazesh, H., Boujar Pour, M., Salari, S., Mohammad Abadi, T. (2013) The effect of ginger powder on performance, carcass characteristics and blood parameters of broilers. Int J Adv Biol Biomed Res. 1: 1645-1651.##Brisbin, J.T., Gong, J., Lusty, C.A., Sabour, P., Sanei, B., Han, Y., Shewen, P.E., Sharif, S. (2008) Influence of in-feed virginiamycin on the systemic and mucosal antibody response of chickens. Poult Sci. 87: 1995–1999.##Castanon, J. I. R. (2007) History of the use of antibiotic as growth promoters in European poultry feeds. Poult Sci. 86: 2466–2471.##Cetin, N., Guclu, B.K., Cetin, E. (2005) The effect of prebiotics and mannan-oligosaccharide on some haematological and immunological parameters in turkey. J Vet Med A. 52: 263–267.##Crowell, P.L. (1999) Prevention and therapy of cancer by dietary monoterpenes. J Nutr. 129: 775s-778s.##Dieumou, F.E., Teguia, A., Kuiate, J.R., Tamokou, J.D., Fonge, N.B., Dongmo, M.C. (2009) Effects of ginger and garlic essential oils on growth performance and gut microbial population of broiler chickens. Livest Res Rural Dev. 21: 25-34.##El-Dakhakhny, M., Mady, N.I., Halim, M.A. (2000) Nigella sativa oil protects against induced hepatotoxicity and improves serum lipid profile in rats. Arzneimittel-Forschung/Drug Res. 50: 832–836.##El-Deek, A.A., Attia, Y.A., Hannfy, M.M. (2003) Effect of anise (Pimpinella anisum), ginger (Zingiber ofﬁcinale roscoe) and fennel (Foeniculum vulgare) and their mixture on performance of broilers. Archiv Für Geﬂügelkunde. 67: 92–96.##Fakhim, R., Ebrahimnezhad, Y., Seyedabadi, H.R., Vahdatpour, T. (2013)  Effect of different concentrations of aqueous extract of ginger (Zingiber officinale) on performance and carcass characteristics of male broiler chickens in wheat-soybean meal based diets. J Biosci Biotechnol. 2: 95-99.##Farinu, G.O., Ademola, S.G., Ajayi, A.O., Babatunde, G.M. (2004) Growth, haematological and biochemical studieson garlic and ginger-fed broiler chickens. Moor J Agric Res. 5: 122–128.##Fukushima, M., Nakano, M. (1996) Effects of a mixture of organisms, Lactobacillus acidophilus or Streptococcus faecalis on cholesterol metabolism in rats fed on a fat- and cholesterol- enriched diet. Br J Nutr. 76: 857- 867.##Gibson, G.R., Roberfroid, M.B. (1995) Dietary modulation of human colonic microbiota: Introducing the concept of prebiotics. J Nutr. 125: 140-142.##Gupta, Y., Sharma, M. (2001) Reversal of pyrogallol-induceddelay in gastric emptying in rats by ginger (Zingiber ofﬁcinale). Methods Find Exp Clin Pharmacol. 23: 501–503.##Hashemi, S.R., Davoodi, H. (2011) Herbal plants and their derivatives as growth and health promoters in animal nutrition. Vet Res Commun. 35: 169-180.##Houshmand, M., Azhar, K., Zulkifli, I., Bejo, M.H., Meimandipour, A., Kamyab, A. (2011) Effects of non-antibiotic feed additives on performance, tibial dyschondroplasia incidence and tibia characteristics of broilers fed low-calcium diets. J Anim Physiol Anim Nutr. 95: 351-358.##Iji, P.A., Saki, A.A., Tivey, D.R. (2001) Intestinal structure and function of broiler chickens on diet supplemented with a mannanoligosaccharide. J Anim Sci. 81: 1186-1192.##Kamran, Z., Mirza, M.A., Ahmad, S., Samad, H.A., Sohail, M.U., Saadullah, M. (2013) Performance of broiler chickens fed mannan oligosaccharides as alternatives to antibiotics from one to twenty-two days of age. J Anim Plant Sci. 23: 1482-1485.##Kececi, O., Oguz, H., Kurtoglu, V., Demet, Ö. (1998) Effects of polyvinylpolypyrrolidone, synthetic zeolite and bentonite on serum biochemical and haematological characters of broiler chickens during aflatoxicosis. Br Poult Sci. 39: 452-458.##Khalaji, S., Zaghari, M., Hatami, K.H., Hedari-Dastjerdi, S., Lotfi, L., Nazarian, H. (2011) Black cumin seeds, Artemisia leaves (Artemisia  sieberi), and Camellia L. plant extract as phytogenic products in broiler diets and their effects on performance, blood constituents, immunity, and cecal microbial population. Poult Sci. 90: 2500-2510.##Khodambashi-Emamia, N., Samiea, A., Rahmania, H.R., Ruiz-Feriab, C.A. (2012) The effect of peppermint essential oils and fructooligosaccharides, as alternatives to virginiamycin, on growth performance, digestibility, gut morphology and immune response of male broilers. Anim Feed Sci Technol. 175: 57-64.##Kim, G.B., Seo, Y.M., Kim, C.H., Paik, I.K. (2011) Effect of dietary prebiotic supplementation on the performance, intestinal microflora, and immune response of broilers. Poult Sci. 90: 75-82.##Lamaty, G., Menut, C., Bessiere, J.M., Zollo, P.H.A., Fekam, F. (1987) Aromatic plants of tropical central Africa. I. Volatile components of two annonaceae from cameroon: Xylopia aethiopica (dunal) A. Richard and Monodora myristica (Gaertn.). Dunal Flav Frag J. 2: 91-94.##Lucas, A.M., Jamroz, C. (1961) Atlas of Avian Hematology. Agriculture Monograph. USDA, Washington, DC, USA.##Maxwell, M.H. (1993) Avian blood leukocyte responses to stress. World’s Poult Sci J. 49: 34-43.##Mehala, C., Moorthy, M. (2008) Effect of Aloe vera and Curcuma longa (Turmeric) on carcass characteristics and biochemical parameters of broilers. Int J Poult Sci. 7: 857-861.##Nasir, Z., Grashorn, M.A. (2010) Effects of Echinacea purpurea and Nigella sativa supplementation on broiler performance, carcass and meat quality. J Anim Feed Sci. 19: 94-110.##Ooi, L.G., Liong, M.T. (2010) Cholesterol-lowering effects of probiotics and prebiotics: a review of in vivo and in vitro findings. Int J Mol Sci. 11: 2499-2522.##Patterson, J.A., Burkhoder, K.M. (2003) Application of prebiotics and probiotics in poultry production. Poult Sci. 82: 627–631.##Pish-Jang, J. (2011) Comparison of effect of Cuminum cyminum and Probiotic on Performance and serum composition of broiler chickens. Ann Biol Res. 2: 630-634.##Platel, K., Srinivasan, K. (2000) Inﬂuence of dietary spices and their active principles on pancreatic digestive enzymes in albino rats. Nahrung/Food. 44: 42–46.##Ravindran, P.N., Babu, K.N. (2005) Ginger the Genus Zingiber, CRC Press. Florida, USA.##Robertfroid, M.B., Delzenne, N. (1998) Dietary fructans. Ann Rev Nutr. 18: 117-143.##Rosen, G. D. (2007) Holo-analysis of the efficacy of Bio-Mos® in turkey nutrition. Br Poult Sci. 48: 27–32.##Saeid, J.M., Mohamed, A.B., Al-Baddy, M.A. (2010) Effect of aqueous extract of ginger (Zingiber ofﬁcinale) on blood biochemistry parameters of broiler. Int J Poult Sci. 9: 944–947.##Seifi, S. (2013) An investigation of the effects of using an enzyme-probiotic combination on broilers performance.  Iran J Vet Med. 7: 299-304.##Shanoon, A.K., Jassim, M.S., Amin, Q.H., Ezaddin, I.N. (2012) Effects of ginger (Zingiber officinale) oil on growth performance and microbial population of broiler Ross 308. Int J Poult Sci. 11: 589-593.##Spring, P., Wenk, C., Dawson, K.A., Newman, K.E. (2000) The effect of dietary mannanoligosaccharides on cecal parameters and the concentrations of enteric bacteria in the ceca of Salmonella-challenged broiler chicks. Poult Sci. 79: 205–211.##Tekeli, A., Kutlu, H.R., Çelik, L. (2011) Effects of z. Officinale and propolis extracts on the performance, carcass and some blood parameters of broiler chicks. Curr Res Poult Sci. 1: 12-23.##Toghyani, M., Toghyani, M., Gheisari, A., Ghalamkari, G., Mohammad rezaei, M. (2010) Growth performance, serum biochemistry and blood hematology of broiler chicks fed different levels of black seed (Nigella sativa) and peppermint (Mentha piperita). Livest Sci. 129: 173-178.##Williams, J., Mallet, S., Leconte, M., Lessire, M., Gabriel, I. (2008) The effects of fructo-oligosaccharides or whole wheat on the performance and digestive tract of broiler chickens. Br Poult Sci. 49: 329–339.##Windisch, W., Schedle, K., Plitzner, C., Kroismayr, A. (2008) Use of phytogenic products as feed additives for swine and poultry. J Anim Sci. 86: E140-E148.##Yalçın, S., Yalçın, S., Uzunoğlu, K., Duyum, H.M., Eltan, Ö. (2012) Effects of dietary yeast autolysate (Saccharomyces cerevisiae) and black cumin seed (Nigella sativa L.) on performance, egg traits, some blood characteristics and antibody production of laying hens. Livest Sci. 145: 13-20.##Zhang, G.F., Yang, Z.B., Wang, Y., Yang, W.R., Jiang, S.Z., Gal, G.S. (2009) Effects of ginger root (Zingiber ofﬁcinale) processed to different particle sizes on growth performance, antioxidant status, and serum metabolites of broiler chickens. Poult Sci. 88: 2159–2166.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>مطالعه آناتومی، هیستولوژی و هیستومورفومتری روده اردک ماهی (Esox lucius)</TitleF>
				<TitleE>Anatomical, histological and histomorphometric study of the intestine of the northern pike (Esox lucius)</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55289.html</URL>
                <DOI>10.22059/ijvm.2015.55289</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: The northern pike Esox lucius is a fresh water species belonging to the Esocidae family. It is a carnivorous fish which mostly feeds on invertebrates and fishes. The morphology of its intestine is very useful for understanding the fish’s digestive physiology, diagnosing some intestinal diseases and formulating suitable feeds. OBJECTIVES: This study was designed to determine the anatomical, histological and histomorphometric properties of the intestine of E. lucius. METHODS: The intestines of five E. lucius were examined in this study. After anatomical dissection, the histological specimens were taken and fixed in 10% formalin. Then, tissue passages were stained with hematoxylin-eosin, and Masson’s trichrome. RESULTS: The anatomical examination showed the short intestine with intestinal coefficient 0.68±0.09 in E. lucius which is a characteristic of the carnivorous species. The histological study revealed that the intestinal wall of E. lucius is composed of tunica mucosa, submucosa, muscularis, and serosa. The muscularis mucosa was not visible in the intestine. The stratum compactum is present between tunica mucosa and tunica submucosa. The histomorphometric results differentiated between three parts in the intestine of E. lucius namely anterior, middle and posterior. The maximum height of mucosal folds was observed in the anterior intestine due to its role in nutrient absorption. The mucosal fold’s height then decreased towards the posterior intestine. The tunica muscularis is significantly thicker in the anterior intestine, and the circular muscle layer is thicker than the longitudinal muscle layer throughout the entire length of the intestine. The posterior intestine possessed large numbers of goblet cells in comparison with other parts of the intestine, to promote elimination of unabsorbed particles. CONCLUSIONS: The results of this study revealed adaptation for the species feeding habits, so as to protect the intestine and increase absorptive processes.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  اردک ماهی (Esox lucius) یک گونه آب شیرین است که متعلق به خانواده Esocidae می‌باشد. این گونه گوشتخوار بوده و از بی مهرگان و ماهیان تغذیه می‌کند. مورفولوژی روده ماهیان برای درک فیزیولوژی گوارش، تشخیص بیماریهای روده‌ای و فرمولاسیون مواد غذایی بسیار سودمند است. هدف: این مطالعه به منظور بررسی خصوصیات آناتومیکی، یافت‌شناسی و هیستومورفومتری روده اردک ماهی صورت گرفت. روش کار: در این مطالعه از تعداد 5 روده اردک ماهی استفاده شد. بعد از بررسی آناتومیکی، نمونه‌های بافت شناسی برداشت و در فرمالین 10٪ ثابت سازی شد و پس از پاساژ بافتی، رنگ‌آمیزی مقاطع به کمک هماتوکسیلین-ائوزین و تری کروم ماسون صورت گرفت. نتایج: بررسی آناتومیکی، روده کوتاه اردک ماهی با ضریب روده‌ای 09/0±68/0 را نشان داد که از خصوصیات ماهیان گوشتخوار محسوب می‌شود. مطالعه بافت شناسی نشان داد که جدار روده اردک ماهی از لایه‌های مخاطی، زیر مخاطی، عضلانی وسروزی تشکیل شده است. عضله مخاطی در جدار روده مشاهده نشد. لایه متراکم مابین لایه‌های مخاطی و زیرمخاطی دیده شد. نتایج هیستومورفومتری سه قسمت قدامی، میانی و خلفی روده اردک ماهی را از هم تفکیک نمود. بیشترین ارتفاع چین‌های مخاطی در روده قدامی بواسطه نقش آن در جذب مواد غذایی مشاهده شد. ارتفاع چین‌های مخاطی بطرف روده خلفی کاهش یافت. لایه عضلانی در روده قدامی ضخیم‌تر بوده و ضخامت لایه عضلانی حلقوی از لایه عضلانی طولی در سراسر طول روده ضخیم تر بوده است. روده خلفی نسبت به سایر قسمت‌های روده دارای تعداد بیشتری از سلول‌های جامی جهت حذف مواد غیرقابل جذب بوده است. نتیجه گیری نهایی: نتایج حاصل از این مطالعه، یک نوع سازگاری این گونه با عادت غذایی را نشان می‌دهد که منجربه حفاظت روده  و افزایش مراحل جذب می‌شود.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>207</FPAGE>
						<TPAGE>211</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>جواد</Name>
						<MidName></MidName>		
						<Family>صادقی نژاد</Family>
						<NameE>Javad</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Sadeghinezhad</FamilyE>
						<Organizations>
							<Organization>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>sadeghinezhad@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>ریحانه</Name>
						<MidName></MidName>		
						<Family>هوشمند عباسی</Family>
						<NameE>Reyhaneh</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Hooshmand Abbasi</FamilyE>
						<Organizations>
							<Organization>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>reyhaneh.hooshmand@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>الهه</Name>
						<MidName></MidName>		
						<Family>هوشمند عباسی</Family>
						<NameE>Elahe</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Dehghani Tafti</FamilyE>
						<Organizations>
							<Organization>Department of Basic Sciences, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>e.dehghani24@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>زهرا</Name>
						<MidName></MidName>		
						<Family>بلوکی</Family>
						<NameE>Zahra</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Boluki</FamilyE>
						<Organizations>
							<Organization>Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>z_boluki@yahoo.com</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Esox lucius</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Intestine</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Anatomy</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Histology</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>histomorphometry</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Bakke, A.M., Tashjian, D.H., Wang, C.F., Lee, S.H., Bai, S.C., Hung, S.S. (2010) Competition between selenomethionine and methionine absorption in the intestinal tract of green sturgeon (Acipenser medirostris). Aquat Toxicol. 96: 62–69.##Cao, X.J., Wang, W.M., Song, F. (2011) Anatomical and histological characteristics of the intestine of the topmouth culter (Culter alburnus). Anat Histol Embryol. 40: 292–298.##Carrassón1, M., Grau, A., Dopazol, L.R., Crespo1, S. (2006) A histological, histochemical and ultrastructural study of the digestive tract of Dentex dentex (Pisces, Sparidae). Histol Histopathol. 21: 579-593.##Chatchavalvanich, K., Marcos, R., Poonpirom, J., Thongpan, A., Rocha, E. (2006) Histology of the digestive tract of the freshwater stingray Himantura signifer Compagno and Roberts, 1982 (Elasmobranchii, Dasyatidae). Anat Embryol (Berl). 211: 507-518.##Craig, J.F. (2008) A short review of pike ecology. Hydrobiologia. 601: 5-16.##Jaroszewska, M., Dabrowski, K., Wilczynska, B., Kakareko, T. (2008) Structure of the gut of the racer goby Neogobius gymnotrachelus (Kessler, 1857). J Fish Biol. 72: 1773–1786.##Kappor, B.G., Smith, H., Verigina, I.A. (1975) The alimentary canal and digestion in teleosts. Adv mar Biol. 13: 109-239.##Kim, Y.S., Samuel, B.H. (2010) Intestinal goblet cells and mucins in health and disease: recent insights and progress. Curr Gastroenterol Rep. 12: 319–330.##Kottelat, M., Freyhof, J. (2007) Handbook of European fresh water fishes. Publications Kottelat, Cornol. Switzerland.##Laikre, L., Miller, L.M., Palmé, A., Palm, S., Kapuscinski, A.R., Thoresson,  G., Ryman, N. (2005) Spatial genetic structure of northern pike (Esox lucius) in the Baltic Sea. Mol Ecol. 14: 1955-1964.##Lokka., G, Austbo, L., Falk, K., Bjerkås, I., Koppang, E.O. (2013) Intestinal morphology of the wild Atlantic salmon (Salmo salar). J Morphol. 274: 859-876.##Moraes, M.F., Freitas-Barbola, I., Duboc, L.F. (2004) Feeding habits and morphometry of digestive tracts of Geophagus brasiliensis (Osteichthyes, Cichlidae), in a lagoon of high tibagi river, parana state, Brazil. Publ UEPG Biol Health Sci Ponta Grossa. 10: 37–45.##Nordrum, S., Bakke-McKellep, A.M., Krogdahl, A., Buddington, R.K. (2000) Effects of soybean meal and salinity on intestinal transport of nutrients in Atlantic salmon (Salmo salar L.) and rainbow trout (Oncorhynchus mykiss). Comp Biochem Physiol B Biochem Mol Biol. 125: 317–335.##Rodríguez Rodríguez, J., González, E., Hernández Contreras, N., Capó, V., García, I. (2004) Morphological and histological comparison of the digestive tract of Gambusia puncticulata and Girardinus metallicus are the fishes used in the biological control of mosquitoes. Rev Cubana Med Trop. 56: 73-76.##Suíçmez, M., Ulus, E. (2005) A study of the anatomy, histology and ultrastructure of the digestive tract of Orthrias angorae Steindachner, 1897. Folia Biol (Krakow). 53: 95-100.##Vieira-Lopes, D.A., Pinheiro, N.L., Sales, A., Ventura, A., Araújo, F.G., Gomes, I.D., Nascimento, A.A. (2013) Immunohistochemical study of the digestive tract of Oligosarcus hepsetus. World J Gastroenterol. 19: 1919-1929.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>ویژگیهای برخی از آنزیم های گوارشی در ماهی صبیتی  Sparidentex hasta</TitleF>
				<TitleE>Characteristics of some digestive enzymes in sobaity, Sparidentex hasta</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55290.html</URL>
                <DOI>10.22059/ijvm.2015.55290</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>Background: Determination of digestive enzymes activity would provide critical information in the design of appropriate diet. Sobaity, Sparidentex hasta is found in the Persian Gulf and  cultured in countries adjacent to it. OBJECTIVES: This study investigated proteolytic, amylase and lipase activities in the intestine of Sparidentex hasta captured from the  Persian Gulf. METHODS: 60 immature S. hasta (mean weight: 520 ± 50g) were captured during summer and autumn of 2012 from Mussa Creek, North West of the Persian Gulf. After euthanization, fish were dissected and the complete digestive tracts (from stomach to anus) were removed. The intestines were separated for each fish and divided to 3 parts; proximal, mid portion and distal. After homogenization, supernatants were removed and enzymes activities were assayed chemically. RESULTS: The highest activity of protease (395.2 ± 32.6 mU mg-1 protein) was recorded in the proximal portion of the intestine compare to the 2 other parts (p&lt;0.05) but amylase and lipase activities did not show a significant difference in 3 parts of the intestine (p&gt;0.05). CONCLUSIONS: This study showed that the pattern of activity of digestive enzymes in S. hasta is consistent with the overall pattern of digestive enzymes activity in carnivorous fish. These data can be used to design special diets for this species.</CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>زمینه مطالعه:  فعالیت آنزیم‌‌های گوارشی نقش مهمی در جذب مواد مغذی و رشد ماهیان دارد. با این وجود اطلاعات موجود در زمینه فعالیت این آنزیم‌ها در ماهیان دریایی خلیج فارس اندک می‌باشد و مطالعات جامعی در این زمینه انجام نگرفته است. هدف: این مطالعه فعالیت آنزیم‌های پروتئولیتیک، لیپاز و آمیلاز در روده ماهی صبیتی، Sparidentex hasta صید شده در خلیج فارس را مورد بررسی قرار می‌دهد. روش کار: در این مطالعه برای دست یابی به اطلاعات پایه در زمینه فعالیت این آنزیم‌ها در روده ماهی صبیتی، تعداد 60 ماهی نابالغ با میانگین وزن g‌50±520 از خور موسی صید گردید. بعد از آسان کشی ماهیان، دستگاه گوارش از دهان تا مخرج جدا و روده به 3 قسمت ابتدایی، میانی و انتهایی تفکیک شد. پس از هموژن سازی روده‌ها، نمونه‌ها سانتریفیوژ و مایع رویی جدا گردید. سپس فعالیت آنزیم‌ها به روش شیمیایی و با استفاده از اسپکتروفتومتر اندازه‌گیری گردید. نتایج: بیشترین فعالیت لیپاز و پروتئاز در قسمت ابتدایی روده ثبت گردید که در مقایسه با دو قسمت دیگر اختلاف معنی‌داری نشان داد (05/0&gt;p) اما فعالیت پروتئاز در 3 بخش روده اختلاف معنی‌داری نشان نداد. نتیجه‌گیری‌نهایی: نتایج این مطالعه نشان داد که الگوی فعالیت آنزیم‌های گوارشی در این ماهی از الگوی کلی فعالیت آنزیم‌های گوارشی در ماهیان گوشتخوار پیروی می‌کند.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>213</FPAGE>
						<TPAGE>218</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>مهدی</Name>
						<MidName></MidName>		
						<Family>جهان تیغ</Family>
						<NameE>Mahdi</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Jahantigh</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Zabol, Zabol, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>jahantighm@gmail.com</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Amylase</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Lipase</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>protease</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Sparidentex hasta</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Persian Gulf</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Bier, M., (1955) Lipases. Methods in Enzymology I. Academic Press, New York. p. 627–642.##Buddington, R.K., Krogdahl, A., Bakke-Mckellep, A.M. (1997) The intestine of carnivorous fish: structure and functions and the relations with diet. Acta Physiol Scand. 161: 67-80.##Chakrabarti, I., Gani, M.A., Chaki, K.K., Sur, R., Misra, K.K. (1995) Digestive enzymes in 11 freshwater teleost fish species in relation to food habit and niche segregation. Comp Biochem Physiol A. 112: 167–177.##Chaudhuri, A., Mukherjee, S., Homechaudhuri, S. (2012) Diet composition and digestive enzymes activity in carnivorous fishes inhabiting mudflats of Indian sundarban estuaries. Turk J Fish Aquat Sci. 12: 265-275.##Correa, C.F., De Aguiar, L.H., Lundstedt, L.M., Moraes, G. (2007). Responses of digestive enzymes of tambaqui (Colossoma macropomum) to dietary cornstarch changes and metabolic inferences. Comp Biochem Physiol A. 147: 857–862.##Cuvier-Peres, A., Kestemont, P. (2002) Development of some digestive enzymes in Eurasian perch larvae Perca fluviatilis. Fish Physiol Biochem. 24: 279–285.##De Almeida, L.C., Lundstedt, L.M., Moraes, G. (2006) Digestive enzyme responses of Tam baqui (Colossoma macropomum) fed on different levels of protein and lipid. Aquac Nutr. 12: 443–450.##Deguara, S., Jauncey, K., Agius, C. (2003) Enzyme activities and pH variations in the digestive tract of gilthead sea bream. J Fish Biol. 62: 1033–1043.##Fountoulaki, E., Alexis, M.N., Nengas, I., Venou, B. (2005) Effect of diet composition on nutrient digestibility and digestive enzyme levels of gilthead sea bream (Sparus aurata L.). Aquacult Res. 36: 1243–1251.##Furne, M., Hidalgo, M.C., Lopez, A., Garcıa-Gallego, M., Morales, A.E., Domezain, A., Domezaine, J., Sanz, A. (2005) Digestive enzyme activities in Adriatic sturgeon Acipenser naccarii and rainbow trout Oncorhynchus mykiss, A comparative study. Aquaculture. 250: 391–398.##Hidalgo, M.C., Urea E., Sanz A. (1999) Comparative study of digestive enzymes in ﬁsh with different nutritional habits, Proteolytic and amylase activities. Aquaculture. 170: 267–28.##Izvekova, G.I., Solovyev, M.M., Kashinskaya, E.N., Izvekov, E.I. (2013) Variations in the activity of digestive enzymes along the intestine of the burbot Lota lota expressed by different methods. Fish Physiol Biochem. 39: 1181-93.##Ji, H., Sun, H.T., Xiong, D.M. (2012) Studies on activity, distribution, and zymogram of protease, α-amylase, and lipase in the paddlefish Polyodon spathula. Fish Physiol Biochem. 38: 603-613.##Liu, Z.Y., Wang, Z., Xu, S.Y., Xu, L.N. (2008) Partial characterization and activity distribution of proteases along the intestine of grass carp, Ctenopharyngodon idella (Val.). Aquac Nutr. 14: 31–39.##Lowry, O.H., Rosebrough, N.J., Farr, A.L., Randall, R.J. (1951) Protein measurement with Folin phenol reagent. J Biol Chem. 193: 265–275.##Lundstedt, L.M., Fernando Bibiano Melo, J., Moraes, G. (2004) Digestive enzymes and metabolic profile of Pseudoplatystoma corruscans (Teleostei: Siluriformes) in response to diet composition. Comp Biochem Physiol B. 137: 331–339.##Metin, K., Akpınar, M.A. (2000) Characterization of lipase in intestine of Oncorhynchus mykiss Walbaum, 1792. Turkish. Turk J Biol. 24: 489-502.##Natalia, Y., Hashim, R., Ali, A., Chong, A. (2004) Characterization of digestive enzymes in a carnivorous ornamental fish, the Asian bony tongue Scleropages formosus (Osteoglossidae). Aquaculture. 233: 305–320.##Perez-Casanova, J.C., Murray, H.M., Gallant, J.W., Ross, N.W., Douglas, S.E., Johnson, S.C. (2004) Bile salt-activated lipase expression during larval development in the haddock (Melanogrammus aeglefinus). Aquaculture. 235: 601–617.##Pérez-Jiménez, A., Cardenete, G., Morales, A.E., Garcia-Alcazar, A., Abellan, E., Hidalgo, M.C. (2009) Digestive enzymatic profile of Dentex dentex and response to different dietary formulations. Comp Biochem Physiol. 154: 157-164.##Phillips, A.M.Jr. (1969) Nutrition, digestion and energy utilization. In: Fish Physiology.  Hoar, W.S., Randall, D.J. (eds.). Academic Press. London, UK. p. 391-432.##Ribeiro, L., Zambonino-Infante, J.L., Cahu, C., Dinis, M.T. (1999) Development of digestive enzymes in larvae of Solea senegalensis, Kaup 1858. Aquaculture. 179: 465–473.##Robyt, J.F., Whelan, W.J. (1968) The h-amylases. In: Starch and Its Derivates. Radley, J.A. (ed.). Academic Press, London, UK. p. 477– 497.##Sklan, D., Prag, T., Lupatsch, I. (2004) Structure and function of the small intestine of the tilapia Oreochromis niloticus, Oreochromis aureus (Teleostei, Cichlidae). Aquac Res. 35: 350–357.##Thompson, K.R., Muzinic, L.A., Engler, L.S., Webster, C.D. (2005) Evaluation of practical diets containing different protein levels, with or without fish meal, for juvenile Australian red claw crayfish (Cherax quadricarinatus). Aquaculture. 244: 241–249.##Tramati, C., Savona, B., Mazzola, A. (2005) A study of the pattern of digestive enzymes in Diplodus puntazzo (Cetti, 1777) (Osteichthyes, Sparidae): evidence for the definition of nutritional protocols. Aquac Int. 13: 89–95.##Ugolev, A.M., Iezuitova, N.N. (1985) Membrane digestion. Structural and functional organization. Usp Fiziol Nauk. Adv Physiol Sci. 16: 3–34.##Walter, H.E. (1984) Proteinases: methods with hemoglobin, casein and azocoll as substrates. In: Methods of Enzymatic Analysis. Bergmeyer, H.U. (ed.). vol. V. Verlag Chemie, Weinheim, Germany. p. 270- 277.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE>
				<ARTICLE>
                <LANGUAGE_ID>1</LANGUAGE_ID>
				<TitleF>تشخیص و درمان کیست فولیکولار فعال در گربه پرشین: گزارش موردی</TitleF>
				<TitleE>Diagnosis and treatment of a functional follicular cyst in a Persian queen cat: A case report</TitleE>
                <URL>https://ijvm.ut.ac.ir/article_55291.html</URL>
                <DOI>10.22059/ijvm.2015.55291</DOI>
                <DOR></DOR>
				<ABSTRACTS>
					<ABSTRACT>
						<LANGUAGE_ID>1</LANGUAGE_ID>
						<CONTENT>In the present report, diagnosis and treatment of a case with follicular ovarian cysts in a 5-year-old Persian queen cat is described. In response to palpation of spines, the queen cat presented herself in lordosis and danced up and down with her rear legs. Trans-abdominal ultrasonography examination showed 2 cysts  in the left ovary of the queen. Serum estrogen assay indicated elevated level of 17 β-estradiol concentration (105 pg/ml). However, progesterone concentration was normal (0.3 ng/ml). Accordingly, the queen was diagnosed with functional follicular cysts. The queen was treated with an administration of hCG intra-muscularly. Thirty (30) days after the administration of hCG, an injection of equine chorionic gonadotropin (eCG) (50 IU) was given intra-muscularly. Natural mating was done with a fertile Persian tom cat. In conclusion, it seems that treatment of functional follicular cysts can be applied to preserve fertility in cats. </CONTENT>
					</ABSTRACT>
					<ABSTRACT>
						<LANGUAGE_ID>0</LANGUAGE_ID>
						<CONTENT>در این گزارش، تشخیص و درمان یک مورد کیست تخمدانی فولیکولی در یک گربه پرشین ماده 5 ساله شرح داده می‌شود.  گربه مورد نظر در ملامسه ناحیه پشت کمر، موقعیت لوردوزیس را به خود گرفته و پاهای عقب را بالا و پایین حرکت می‌داد.بررسی سونوگرافی ناحیه شکم دو کیست در تخمدان چپ گربه نشان داد. ارزیابی استروژن سرم خون، غلظت بالای 17 بتا_استرادیول (pg/mL 105) را نشان داد. با این حال غلظت پروژسترون نرمال (ng/mL 3/0) بود. بر این اساس، گربه مبتلا به کیست فولیکولار فعال تشخیص داده شد. حیوان مذکور با گنادوتروپین جفتی انسان (hCG) به صورت داخل عضلانی تحت درمان قرار گرفت. 30 روز پس از تجویز hCG، یک تزریق گنادوتروپین جفتی اسب (eCG) (50 واحد بین المللی) به صورت داخل عضلانی انجام شد. جفت‌گیری طبیعی با یک گربه نر پرشین بارور انجام گرفت. در نتیجه، به نظر می‌رسد که درمان دارویی کیست‌های فولیکولار فعال را می‌توان به منظور حفظ باروری در گربه سانان به ک ار گرفت.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>219</FPAGE>
						<TPAGE>221</TPAGE>
					</PAGE>
				</PAGES>
	
				<AUTHORS><AUTHOR>
						<Name>رضا</Name>
						<MidName></MidName>		
						<Family>یوسفی</Family>
						<NameE>Reza</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Youssefi</FamilyE>
						<Organizations>
							<Organization>1Department of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
2Theriogenology Association, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>youssefi.dvm@gmail.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>رضا</Name>
						<MidName></MidName>		
						<Family>یوسفی</Family>
						<NameE>Parviz</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Tajik</FamilyE>
						<Organizations>
							<Organization>Department of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>ptajik@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>وریا</Name>
						<MidName></MidName>		
						<Family>توحیدی</Family>
						<NameE>Vrya</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Tohidi</FamilyE>
						<Organizations>
							<Organization>Department of Clinical Sciences, Faculty of Veterinary Medicine, Karaj Branch, Islamic Azad University, Karaj, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>youssefi.dvm@ut.ac.com</Email>			
						</EMAILS>
					</AUTHOR><AUTHOR>
						<Name>وحید</Name>
						<MidName></MidName>		
						<Family>اکبری نژاد</Family>
						<NameE>Vahid</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Akbarinejad</FamilyE>
						<Organizations>
							<Organization>1Department of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
2Theriogenology Association, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran</Organization>
						</Organizations>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>youssefi.dvm5@ut.ac.ir</Email>			
						</EMAILS>
					</AUTHOR></AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Follicular ovarian cyst</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>cystic ovarian disease</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Cat</KeyText>
					</KEYWORD></KEYWORDS>
				<REFRENCES>
				<REFRENCE>
				<REF>Boomsma, R.A., Jaffe. R.C., Verhage, H.G. (1982) The uterine progestational response in cats: changes in morphology and progesterone receptors during chronic administration of progesterone to estradiol-primed and non primed animals. Biol Reprod. 26: 511–521.##Boomsma, R.A., Verhage, H.G. (1982) The uterine progestational response in cats: ultrastructural changes during chronic administration of progesterone to estradiol-primed and nonprime animals. Am J Anat. 164: 243–254.##Bristol-Gould, S., Woodruff, T.K. (2006) Folliculogenesis in the domestic cat (Felis catus). Theriogenology. 66: 5–13.##Gharagozlou, F., Youssefi, R., Akbarinejad, V., Sasani, F., Taghizadeh-Jahed, M., Shahpoorzadeh, T., Valaie Moradipor, H., Hasani, N., Atashbaste, M. (2014) Evaluation of serum anti-Müllerian hormone (AMH) in a Persian queen cat with bilateral cystic ovarian disease. Comp Clin Pathol. 23: 237–239.##Gelberg, H.B., McEntee, K., Heath, E.H. (1984) Feline cystic rete ovarii. Vet Pathol. 21: 304–307.##Johnston, S.D., Root Kustritz, M.V., Olson, P.S. (2001) Disorders of the feline ovaries. In: Canine and Feline Theriogenology. Johnston, S.D., Root Kustritz, M.V., Olson, P.S. (eds.). Saunders, Philadelphia, USA. p. 453–462.##Ortega-Pacheco, A., Gutiérrez-Blanco, E., Jiménez-Coello, M. (2012) Common lesions in the female reproductive tract of dogs and Cats. Vet Clin Small Anim. 42: 547–559.##Wildt, D.E., Kinney, G.M., Seager, S.W.J. (1978) Gonadotropin induced reproductive cyclicity in the domestic cat. Lab Anim Sci. 28: 301-307.##Wildt, D.E., Phillips, L.G., Simmons, L.G., Goodrowe, K.L., Howard, J.G., Brown, J.L., Bush, M. (1987) Seminal-endocrine characteristics of the tiger and the potential for artificial breeding. In: Tigers of the World: The Biology, Biopolitics, Management and Conservation of an Endangered Species. Tilson, R.L., Seal, U.S. (eds.). Noyes Publications. Park Ridge, USA. p. 255-79.##Wildt, D.E., Schiewe, M.C., Schmidt, P.M., Goodrowe, K.L., Howard, J.G., Phillips, L.G., O’Brien, S.J., Bush, M. (1986) Developing animal node1 systems for embryo technologies in rare and endangered Wildlife. Theriogenology. 25: 33-51.##</REF>
						</REFRENCE>
					</REFRENCES>
			</ARTICLE></ARTICLES>
</JOURNAL>

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