نوع مقاله : مقاله پژوهشی
نویسندگان
1 گروه زیست شناسی، دانشکده علوم پایه، واحد تهران مرکزی، دانشگاه آزاد اسلامی، تهران، ایران
2 گروه فیزیولوژی، دانشکده دامپزشکی، واحد گرمسار، دانشگاه آزاد اسلامی، گرمسار، ایران
چکیده
کلیدواژهها
Introduction
Pulmonary hypertension syndrome (PHS) results from developments in both the respiratory and cardiovascular systems (Babaahmadi Milani et al., 2020). PHS is a metabolic disorder and multifactorial syndrome caused by interactions among environmental, physiological and genetic factors (Hosseinian et al., 2021). Also, PHS is defined by hypoxemia, cardiopulmonary overload, venous and cardiac obstruction, and right ventricular hypertrophy (Dimopoulos et al., 2018). Heart failure is common in modern broilers with a high growth rate and the respiratory system cannot provide efficient ventilation and gas exchange, leading to hypoxia (Majdi Abdelfaraj et al., 2023). Increased levels of blood flow, stroke volume, cardiac output, vascular pressure in the pulmonary, right ventricular hypertrophy and pressure in the pulmonary arteries and capillaries are known as the result of compensatory effects of the cardiovascular system (Yadollah et al., 2023). This condition eventually causes PHS (Hassanpour et al., 2014). Studies have shown that during this syndrome, many oxidants are produced in the affected tissues (Hassanpour et al., 2015). Also, various studies investigated the most obvious environmental factors that play a role in PHS. These factors are altitude, cold stress, lighting, air quality, ventilation, high nutrient density rations, and incubation environment (Vandana et al., 2021; Ipek & Sahan, 2006; Ghiasi et al., 2023).
PHS involves complex processes and includes pathological pathways in vascular remodeling related to inflammation, vascular fibrosis, and apoptosis (Solano-Gálvez et al., 2018). Apoptosis typically occurs during growth and aging as a hemostatic mechanism to maintain tissue cell populations. Apoptosis is a defense mechanism in immune reactions or when disease damages cells (Kiraz et al., 2017). Apoptosis is a highly conserved process with multiple pathways involved in several physiological and pathological phenomena (Redza-Dutordoir & Averill-Bates, 2016; Solano-Gálvez et al., 2018). At the molecular level, major changes in this process consist of cell shrinkage, formation of apoptotic bodies, caspase activation, chromatin condensation, and eventually DNA fragmentation (Solano-Gálvez et al., 2018). The leading players in apoptosis orchestration are caspases, the special cysteine proteases with a proteolytic function (Nicholson & Thornberry, 1997). Caspases break down other cytoplasmic proteins containing aspartic acid residues (Nicholson & Thornberry, 1997). Elevation of both caspase1 (CASP1) (stimulated by inflammatory agents) and caspase2 (CASP2) could be used as evidence for the early steps of the apoptotic process (Igney & Krammer, 2002).
On the other hand, garlic has been a food supplement since ancient times. Various studies indicated garlic has preventive and therapeutic effects on many diseases, such as heart problems, intestinal disorders, atherosclerosis, thrombosis, dementia, cancer and diabetes (Sobenin et al., 2019; Ohtani & Nishimura, 2020). In addition, several experiments have reported garlic powder’s (GP) antioxidant and anti-hypertensive properties in different animal models (Puvača et al., 2015; Wei & Lau, 1998). As a potent antioxidant, it protects cells against oxidative damage, reactive oxygen species (ROS) damage, and lipid peroxidation (Oloruntola et al., 2023; Askari et al., 2021; Yang et al., 2019).
So, the purpose of the study reported is to determine the protective effect of GP on the level of CASP1 and CASP2, as important apoptosis markers, in the lungs and heart ventricles of broiler chickens following the PHS induction by triiodothyronine (T3).
Materials and Methods
Study animals
Ninety fast-growing 1-day-old chickens (Ross 308) were divided randomly into three groups (Sham, PHS, and PHS+GP). Each group consisted of 30 chickens with three replicate pens per group and ten chickens per pen under the same and controlled conditions, such as humidity, ventilation, temperature, light cycle and vaccination. During the experiments, the chickens were kept according to the instructions mentioned in the care and use of laboratory animals (Clark, 1997) and the Animal Care Committee of the Deputy of Medical Sciences, Islamic Azad University approved all the experimental steps. Chickens were reared in the floor pens (wood shaving litter) for three or seven weeks under standard conditions, with ad libitum access to water and a standard basal diet in mash form. In the second week, in the PHS and PHS+GP groups, thyroid hormone, i.e. T3 (Sigma Chemical Co.), was added to the diet (1.5 mg/kg). For the GP group, GP (1%) was used as a treatment after the first week of rearing (Hassanpour et al., 2014; Arab et al., 2006).
Assessment of right ventricular hypertrophy
During the breeding period, sampling was done on days 21 and 49 for the three groups (n=15). Sampling was carried out by cutting the carotid arteries and veins. Then, the abdominal area was opened, and the arteries connected to the heart were cut. Finally, the heart was removed from the chest. After examining the appearance and weighing of the left and right ventricles (RV), the RV was dissected free of the left ventricle and septum. The weight of the RV was measured and the ratio of the RV to the total ventricle (RV/TV) weight was calculated (Hassanpour et al., 2014; Cueva et al., 1974; Wideman, 2001).
RNA extraction of lung and RV tissues
After collecting chickens’ lungs and RVs, tissues were immediately immersed in liquid nitrogen and kept at -80 °C, where they were stored until RNA extraction. Total RNA was extracted from tissues using TRIzol reagent (Invitrogen, Karlsruhe, Germany). After the homogenizing tissues, chloroform was added to the mixture and centrifuged. The total RNA was settled in the upper aqueous phase. Isopropanol was used to precipitate RNA, and the RNA pellet was washed with ethanol (75%). The extracted RNAs were resuspended in DEPC-treated water. DNase was used to remove eventual residual DNA, and the RNA concentration was then measured and qualified by spectrophotometry and gel electrophoresis (Hassanpour et al., 2014).
Semi-quantitative RT-PCR
All primers used in the current study are listed in Table 1. A cDNA synthesis kit synthesized cDNA using reverse transcriptase, Oligo (dt) and random hexamer. A reverse transcription polymerase chain reaction (RT-PCR) was run, followed by 40 cycles. Beta-actin expression was measured as an endogenous control. Finally, the CASP1 and CASP2 expression ratio to the β-actin (ACBT) was calculated using Photo-Capt Image Software, version 99. The density of bands was calculated and relative densities were expressed as CASP1/ACBT and CASP2/ACBT (Hassanpour et al., 2011; Teshfam et al., 2006).
Statistical analysis
The results of the experiments were presented as Mean±SEM. The statistical analysis was carried out using GraphPad Prism Software, version 6. Comparisons were made between sham, PHC and PHC+GP using the one-way analysis of variance (ANOVA). P<0.05 was considered a significant difference among groups.
Results
Effect of GP on right ventricular hypertrophy
The ratio of RV/TV as an indicator of right ventricular hypertrophy and pulmonary hypertension was measured in different groups on days 21 and 49 (Figure 1). Our data showed no significant difference between all groups on day 21 (P≤0.05). Surprisingly, this ratio increased on day 49 in the PHS group by about 1.74-fold compared to the sham group (P<0.001). Also, treatment with GP decreased RV/TV to 69.18% compared to the PHS group (P<0.001). Besides, an increase of about 1.2-fold was seen in the PHS+GP group compared to the sham (P<0.05).
Effect of GP on the expression of CASP1 and CASP2 in the lungs of PHS chickens
Gene expression of CASP1 and CASP2 was determined by semi-quantitative RT-PCR in broiler chicken lungs of different groups, as shown in Figure 2. A one-way ANOVA analysis of CASP1 and CASP2 expressions in the lung showed no significant change between sham, PHS, and PHS+GP groups on day 21 (P≤0.05).
However, our result showed an increase of about 2.97 and 2.51 folds in the CASP1 and CASP2 expressions of PHS compared to the sham group on day 49 (P<0.001). Also, consumption of GP (PHS+GP group) significantly reduced the ratio of CASP1 and CASP2/ACBT to about 42.01% and 40.6% compared with PHS, respectively (P<0.001). Besides, the CASP1 expression of this group (PHS+GP) increased by about 1.25 folds compared to the sham (P<0.05).
Effect of GP on the expression of CASP1 and CASP2 in the RVs of PHS chickens
RT-PCR determined the expression of CASP1 and CASP2 genes in broiler chickens’ RVs in treated and untreated groups (Figure 3). On day 21, our result revealed that the expression of CASP1 in the PHS group increased by about 1.04 folds compared to the sham group (P<0.001). Also, this gene in the PHS+GP group was significantly decreased to 62.5% compared with the PHS group (P<0.001). At the same time, the ratio CASP2/ACBT did not show any significant alterations in all three groups on day 21 (P≤0.05) (Figure 3A and 3B).
Moreover, one-way ANOVA analysis of day 49 results indicated the expression of CASP1 and CASP2 elevated in the PHS group by about 2.25 and 1.34 folds compared to the sham group, respectively (P<0.001). Also, the consumption of GP (PHS+GP group) could decrease the ratio of CASP1/ACBT and CASP2/ACBT to about 52.0% and 44.67% when compared to the PHS group (P<0.001). Besides, the comparison of PHS+GP with sham showed an increase of about 1.19 and 1.51 folds for CASP1 (P<0.05) and CASP2 (P<0.01) genes, respectively (Figure 3C and 3D).
Discussion
In the present study, we evaluated the effect of GP treatment as an antioxidant during the PHS in fast-growing chickens. To propose a molecular mechanism, we assessed the anti-apoptotic effect of GP on the reduction of CASP1 and CASP2 gene expressions in the lung and RV of chickens.
Broilers have an innate potential to cause PHS. Consistent with the experiment of Wideman (2001), our result showed that increasing the RV/TV ratio can be detected during PHS. Studies reported a positive relation between hypertrophy of right ventricular and pulmonary arterial pressure. Based on our results, using GP as a treatment could modulate pulmonary hypertensive response and decrease hypertrophy and dilation of the heart. Allicin is an effective garlic material, and experiments have reported that allicin in garlic could prevent coronary endothelial dysfunction and RV hypertrophy (El-Sheakh et al., 2006). In addition, Sobenin et al. (2009) observed that garlic can reduce systolic and diastolic blood pressure and may defend the heart against hypertrophy. Several mechanisms of action have been proposed for the GP effect on blood pressure, including the release of nitric oxide, a vasodilatory factor.
Apoptosis occurs in the cells during both physiological and pathological conditions. Over the past few decades, many studies have shown that apoptosis may be an essential cell death method during cardiomyopathies in both human and animal models (Pertiwi et al., 2022; Blondeau et al., 2019). Wideman (2001) introduced a threshold for RV/TV ratio as an indicator to cause PHS, and our results did not reach the threshold at day 21 (P≤0.05). Maybe it was because we also did not see a considerable change in the apoptosis at day 21. Also, evidence demonstrated susceptibility to apoptosis in ventricle hypertrophy rises with age (Kim et al., 2005).
Our results showed that PHS induction during 49 days increased the expression of CASP1 and CASP2 genes in chickens’ lungs and RV (P<0.001). These results approved our previous work that showed apoptosis increased in the heart and lungs of broiler chickens suffering PHS at day 49 (Hassanpour et al., 2014). The release of cytochrome C from the mitochondria into the cytoplasm and the cleavage and activation of caspases initiate the onset of the apoptotic pathway. Eventually, caspase activation leads to the fragmentation of various cytoplasmic proteins and DNA (Kang & Izumo, 2000). Studies on animal experimental models and human tissues have reported an essential role for CASP1 in developing heart failure as a potent proapoptotic agent (Merkle et al., 2007). It has also been observed that due to heart failure, the expression of the CASP2 gene is increased in the ventricle, which is a sign of apoptosis (Heinke et al., 2001).
On the other hand, progressive hypoxia occurs in the chickens’ tissues with pulmonary hypertension and can increase the free radicals and oxidant levels of affected tissues. As free radicals have been reported to be essential in activating caspases and inducing apoptosis (Solano-Gálvez et al., 2018), using a potent antioxidant seems to be a promising treatment option for PHS.
Since ancient times, garlic has been widely used as a food additive or growth promoter and as a medicinal plant to prevent and treat many heart diseases. Our investigation revealed that it can be effective as a therapeutic supplement for PHS by reducing the RV hypertrophy and apoptosis gene expression, including CASP1 and CASP2. Garlic has many bioactive ingredients such as allicin, alliin, ajoene, diallyl sulfide, dithiin and S-allyl cysteine that could target different molecular pathways and be used as a natural herbal food additive to improve the growth of broilers (Ziarlarimi et al., 2011; Khan et al., 2012). Garlic can act as a nitric oxide donor and also have a relaxing effect directly on the aortic and heart muscles (Sobenin et al., 2009). In addition, garlic affects blood pressure by inhibiting Na/K-ATPase in the kidney, which triggers diphasic urinary and natriuretic responses. It has been reported that garlic components may increase membrane polarization through potassium ion channels that close Ca2+ channels, leading to cell death inhibiting (Sobenin et al., 2009). Gao et al. (2021) show that GP consumption can down‐regulate the expression of caspase genes. Approving our results, Ismail et al. (2021) demonstrated that the consumption of GP as a supplementary diet positively affected performance, safety, antioxidant level, and physiological characteristics of broilers.
Conclusion
Taken together, our investigation revealed that GP can be used as a supplementary diet to prevent PHS complications, reduce RV hypertrophy, and decrease apoptosis in the hearts and lungs of broilers.
Ethical Considerations
Compliance with ethical guidelines
This study was approved by the Ethics Committee of Islamic Azad University, Garmsar Branch.
Funding
This research was supported by Islamic Azad University, Garmsar Branch (Grant No.: 4426).
Authors' contributions
All authors equally contributed to preparing this article.
Conflict of interest
The authors declared no conflict of interest.
Acknowledgments
The authors appreciate Islamic Azad University, Garmsar Branch, for supporting this research.
References
Arab, H. A., Jamshidi, R., Rassouli, A., Shams, G., & Hassanzadeh, M. H. (2006). Generation of hydroxyl radicals during ascites experimentally induced in broilers. British Poultry Science, 47(2), 216-222. [PMID]
Askari, M., Mozaffari, H., Darooghegi Mofrad, M., Jafari, A., Surkan, P. J., & Amini, M. R., et al. (2021). Effects of garlic supplementation on oxidative stress and antioxidative capacity biomarkers: A systematic review and meta-analysis of randomized controlled trials. Phytotherapy Research: PTR, 35(6), 3032-3045. [DOI:10.1002/ptr.7021] [PMID]
Blondeau, B., Orlando, A., Jarvis, S., Banton, K., Berg, G. M., & Patel, N., et al. (2019). Variability in pelvic packing practices for hemodynamically unstable pelvic fractures at US level 1 trauma centers. Patient Safety in Surgery, 13, [DOI:10.1186/s13037-019-0183-7] [PMID] [PMCID]
Clark, J. D., Gebhart, G. F., Gonder, J. C., Keeling, M. E., & Kohn, D. F. (1997). Special report: The 1996 guide for the care and use of laboratory animals. ILAR Journal, 38(1), 41–48. [DOI: 10.1093/ilar.38.1.41]
Cueva, S., Sillau, H., Valenzuela, A., & Ploog, H. (1974). High altitude induced pulmonary hypertension and right heart failure in broiler chickens. Research in Veterinary Science, 16(3), 370-374. [DOI:10.1016/S0034-5288(18)33737-8] [PMID]
Dimopoulos, K., Diller, G. P., Opotowsky, A. R., D'Alto, M., Gu, H., & Giannakoulas, G., et al. (2018). Definition and management of segmental pulmonary hypertension. Journal of the American Heart Association, 7(14), e008587. [DOI:10.1161/JAHA.118.008587] [PMID] [PMCID]
El-Sheakh, A. R., Ghoneim, H. A., Suddek, G. M., & Ammar, E. S. M. (2016). Attenuation of oxidative stress, inflammation, and endothelial dysfunction in hypercholesterolemic rabbits by allicin. Canadian Journal of Physiology and Pharmacology, 94(2), 216–224. [DOI:10.1139/cjpp-2015-0267] [PMID]
Gao, X., Yanan, J., Santhanam, R. K., Wang, Y., Lu, Y., & Zhang, M., et al. (2021). Garlic flavonoids alleviate H2 O2 induced oxidative damage in L02 cells and induced apoptosis in HepG2 cells by Bcl-2/Caspase pathway. Journal of Food Science, 86(2), 366-375. [DOI:10.1111/1750-3841.15599] [PMID]
Ghiasi, S., Zendehdel, M., Haghbinnazarpak, H., Asghari, A., & Sheikhi, N. (2023). Central and peripheral effects of lipopolysaccharide on food choice and macronutrient selection in meat-type chick. Archives of Razi Institute, 78(3), 843-851. [PMID]
Hassanpour, H., Khalaji-Pirbalouty, V., Nasiri, L., Mohebbi, A., & Bahadoran, S. (2015). Oxidant and enzymatic antioxidant status (gene expression and activity) in the brain of chickens with cold-induced pulmonary hypertension. International Journal of Biometeorology, 59(11), 1615-1621. [DOI:10.1007/s00484-015-0968-z] [PMID]
Hassanpour, H., Momtaz, H., Shahgholian, L., Bagheri, R., Sarfaraz, S., & Heydaripoor, B. (2011). Gene expression of endothelin-1 and its receptors in the heart of broiler chickens with T(3)-induced pulmonary hypertension. Research in Veterinary Science, 91(3), 370-375. [DOI:10.1016/j.rvsc.2010.09.019] [PMID]
Hassanpour, H., Teshfam, M., Momtaz, H., Zarei, H., & Bahadoran, S. (2014). Caspase-1,-2, and-3 gene expression is enhanced in the heart and lung of chickens with pulmonary hypertension (ascites). Turkish Journal of Veterinary & Animal Sciences, 38(2), 133-137. [DOI:10.3906/vet-1302-37]
Heinke, M. Y., Yao, M., Chang, D., Einstein, R., & dos Remedios, C. G. (2001). Apoptosis of ventricular and atrial myocytes from pacing-induced canine heart failure. Cardiovascular Research, 49(1), 127-134. [DOI:10.1016/s0008-6363(00)00242-x] [PMID]
Hosseinian, S. A., Abdi Hacheso, B., Nazifi, S., Hashemi Hazaveh, S. A., Hashemi Tabar, S. H., & Rezapoor, R. (2021). Cardioprotective and hepatoprotective activity of silymarin in broiler chickens fed on mash and pellet diets. Iranian Journal of Veterinary Medicine, 15(1), 104-121. [DOI:10.22059/IJVM.2020.302033.1005084]
Igney, F. H., & Krammer, P. H. (2002). Death and anti-death: tumour resistance to apoptosis. Nature Reviews. Cancer, 2(4), 277-288. [DOI:10.1038/nrc776] [PMID]
Ipek, A., & Sahan, U. (2006). Effects of cold stress on broiler performance and ascites susceptibility. Asian-Australasian Journal of Animal Sciences, 19(5), 734-738. [DOI:10.5713/ajas.2006.734]
Ismail, I. E., Alagawany, M., Taha, A. E., Puvača, N., Laudadio, V., & Tufarelli, V. (2021). Effect of dietary supplementation of garlic powder and phenyl acetic acid on productive performance, blood haematology, immunity and antioxidant status of broiler chickens. Animal Bioscience, 34(3), 363-370. [DOI:10.5713/ajas.20.0140] [PMID] [PMCID]
Kang, P. M., & Izumo, S. (2000). Apoptosis and heart failure: A critical review of the literature. Circulation Research, 86(11), 1107-1113. [DOI:10.1161/01.res.86.11.1107] [PMID]
Khan, R. U., Nikousefat, Z., Tufarelli, V., Naz, S., Javdani, M., & Laudadio, V. (2012). Garlic (Allium sativum) supplementation in poultry diets: Effect on production and physiology. World’s Poultry Science Journal, 68(3), 417-424. [DOI:10.1017/S0043933912000530]
Kim, S. H., Choi, J. Y., Sihn, C. R., Suh, E. J., Kim, S. Y., & Choi, K. D., et al. (2005). Induction of apoptosis in chicken oviduct cells by C2-ceramide. Molecules and Cells, 19(2), 185-190. [DOI:10.1007/s10059-010-0026-y] [PMID]
Kiraz, Y., Adan, A., Kartal Yandim, M., & Baran, Y. (2016). Major apoptotic mechanisms and genes involved in apoptosis. Tumour Biology: The Journal of The International Society for Oncodevelopmental Biology and Medicine, 37(7), 8471-8486. [DOI:10.1007/s13277-016-5035-9] [PMID]
Majdi Abdelfaraj, K., Mohamed Idris, A., & Mohamed M, I. (2023). Effect of diet supplemented with different levels of moringa powder on growth performance, carcass characteristics, meat quality, hematological parameters, serum lipids, and economic efficiency of broiler chickens. Archives of Razi Institute, 78(5), 1647-1656. [DOI:10.32592/ARI.2023.78.5.1647] [PMID] [PMCID]
Merkle, S., Frantz, S., Schön, M. P., Bauersachs, J., Buitrago, M., & Frost, R. J., et al. (2007). A role for caspase-1 in heart failure. Circulation Research, 100(5), 645-653. [DOI:10.1161/01.RES.0000260203.55077.61] [PMID]
Nicholson, D. W., & Thornberry, N. A. (1997). Caspases: Killer proteases. Trends in Biochemical Sciences, 22(8), 299–306. [DOI:10.1016/s0968-0004(97)01085-2] [PMID]
Ohtani, M., & Nishimura, T. (2020). The preventive and therapeutic application of garlic and other plant ingredients in the treatment of periodontal diseases. Experimental and Therapeutic Medicine, 19(2), 1507-1510. [DOI:10.3892/etm.2019.8382] [PMID] [PMCID]
Oloruntola, O. D., Ayodele, S. O., Jimoh, O. A., Oloruntola, D. A., & Osowe, C. O. (2023). Nutraceutical effects of justicia carnea leaf powder supplementations on performance, blood indices, heat shock protein 70, oxidative deoxyribonucleic acid damage biomarkers and intestinal microbes of broiler chickens, under tropical condition. Archives of Razi Institute, 78(4), 1217-1223. [DOI:10.32592/ARI.2023.78.4.1217] [PMID] [PMCID]
Pertiwi, H., Rochmy, S. E., & Chwen, L. T. (2023). Detrimental effect of tannin on growth performance, visceras weight and blood biochemistry in broiler chickens reared under tropical area. Archives of Razi Institute, 78(4), 1269-1275. [DOI:10.32592/ARI.2023.78.4.1269]
Puvača, N., Ljubojević, D., Kostadinović, L. J., Lukač, D., Lević, J., & Popović, S., et al. (2015). Spices and herbs in broilers nutrition: Effects of garlic (Allium sativum L.) on broiler chicken production. World’s Poultry Science Journal, 71(3), 533-538. [DOI:10.1017/S0043933915002214]
Redza-Dutordoir, M., & Averill-Bates, D. A. (2016). Activation of apoptosis signalling pathways by reactive oxygen species. Biochimica et Biophysica Acta, 1863(12), 2977-2992. [DOI:10.1016/j.bbamcr.2016.09.012] [PMID]
Sobenin, I. A., Andrianova, I. V., Fomchenkov, I. V., Gorchakova, T. V., & Orekhov, A. N. (2009). Time-released garlic powder tablets lower systolic and diastolic blood pressure in men with mild and moderate arterial hypertension. Hypertension Research: Official Journal of the Japanese Society of Hypertension, 32(6), 433-437. [DOI:10.1038/hr.2009.36] [PMID]
Sobenin, I. A., Myasoedova, V. A., Iltchuk, M. I., Zhang, D. W., & Orekhov, A. N. (2019). Therapeutic effects of garlic in cardiovascular atherosclerotic disease. Chinese Journal of Natural Medicines, 17(10), 721-728. [DOI:10.1016/S1875-5364(19)30088-3] [PMID]
Solano-Gálvez, S. G., Abadi-Chiriti, J., Gutiérrez-Velez, L., Rodríguez-Puente, E., Konstat-Korzenny, E., & Álvarez-Hernández, D. A., et al. (2018). Apoptosis: Activation and inhibition in health and disease. Medical Sciences (Basel, Switzerland), 6(3), 54. [DOI:10.3390/medsci6030054] [PMID] [PMCID]
Teshfam, M., Brujeni, G. N., & Hassanpour, H. (2006). Evaluation of endothelial and inducible nitric oxide synthase mRNA expression in the lung of broiler chickens with developmental pulmonary hypertension due to cold stress. British Poultry Science, 47(2), 223-229. [DOI:10.1080/00071660600611169] [PMID]
Vandana, G. D., Sejian, V., Lees, A. M., Pragna, P., Silpa, M. V., & Maloney, S. K. (2021). Heat stress and poultry production: Impact and amelioration. International Journal of Biometeorology, 65(2), 163-179. [DOI:10.1007/s00484-020-02023-7] [PMID]
Wei, Z., & Lau, B. H. (1998). Garlic inhibits free radical generation and augments antioxidant enzyme activity in vascular endothelial cells. Nutrition Research, 18(1), 61-70. [DOI:10.1016/S0271-5317(97)00200-5]
Wideman, R. F. (2001). Pathophysiology of heart/lung disorders: pulmonary hypertension syndrome in broiler chickens. World’s Poultry Science Journal, 57(3), 289-307. [DOI:10.1079/WPS20010021]
Yadollah, B., & Zahra Roudbari, A. B. (2023). Broiler heart muscle monoaminergic receptors alteration in response to chronic heat stress: Based on transcription analysis. Archives of Razi Institute, 78(5), 1594-1602. [DOI:10.32592/ARI.2023.78.5.1594] [PMID] [PMCID]
Yang, F., Liu, X., Wang, H., Deng, R., Yu, H., & Cheng, Z. (2019). Identification and allelopathy of green garlic (allium sativum l.) volatiles on scavenging of cucumber (cucumis sativus l.) reactive oxygen species. Molecules (Basel, Switzerland), 24(18), 3263. [DOI:10.3390/molecules24183263] [PMID] [PMCID]
Ziarlarimi, A., Irani, M., Gharahveysi, S., & Rahmani, Z. (2011). Investigation of antibacterial effects of garlic (Allium sativum), mint (Menthe spp.) and onion (Allium cepa) herbal extracts on Escherichia coli isolated from broiler chickens. African Journal of Biotechnology, 10(50), 10320-10322. [Link]