تاثیر پیوند صفاقی اتوژن تقویت شده با پروتئین غنی از پلاسما-پلاکت ها بر ترمیم پارگی تاندون آشیل القا شده در سگ

Introduction

Tendon injuries commonly occur and constitute one of the greatest challenges for orthopedic surgery. The healing process of such cases is slow and treatment might require prolonged rehabilitation (Denitsa et al., 2015). In dogs, both partial and total rupture of Achilles tendon is not an uncommon traumatic problem (Taniguchil et al., 2018). Several therapeutic choices have been used to repair the ruptured tendons; these included traditional suturing, autografting, allografting, and synthetic prostheses (Denitsa et al., 2015). Treatment of the ruptured Achilles tendon is continued to be controversial; however, the most frequently applied methods are conservative, percutaneous, and surgical repair (Greca et al., 2005). Re-rupture after treatment is the major problem; Thus, surgical intervention is advisable to restore tendon integrity, strength, and functional (Spinella et al., 2010). Various studies have assessed the efficacy of utilizing several materials that have the potential to improve

the healing process and tendon regeneration without the development of fibrotic tissue. For instance, polypropylene mesh, collagen fiber implantation, pericardium, small intestine submucosa, dermal patch, mesenchymal stem cells, vein graft, platelet-rich plasma and omentum (Jahani et al., 2015; Canapp et al., 2016; Bellenger, 2003). The peritoneum is a serous membrane covered by mesothelial cells and supported by a stromal layer. The stromal layer is composed of elastic and collagen fiber, mast cells, macrophages, lymphocytes, adipose cells, and glycosaminoglycans (Konig et al., 2004). The utilization of the peritoneum is based on the capacity of its relative cells to release growth factors such as transforming growth factor, fibroblast growth factor, and epidermal growth factor, which demonstrated a positive effect on the healing process (Hosgood, 2003). The application of PRP enables tendon lesions to recuperate and eliminate signs of inflammation (Bellido et al., 2018). Ultrasonographic evaluation of the normal Achilles tendon was firstly reported in 1997, where a report investigated the effectiveness of ultrasonography as a diagnostic imaging procedure in orthopedic problems in small animals (Kramer et al., 1997). Based on the sonographic echotexture pattern, a previous study on canine Achilles tendon injury demonstrated that ultrasonographic examination is insufficient for differentiation between the partial and complete rupture of the Achilles tendon (Rivers, 1997). However, another relevant study indicated that ultrasonography can be employed to categorize the partial ruptures into deep or superficial ruptures (Kramer et al., 2001). Additionally, a considerable amount of literature has been published on the using of ultrasounds as a diagnostic tool of Achilles tendon affections in dogs (Baltzer and Rist, 2009; Case et al., 2013; Spinella et al., 2010). Therefore, the present study was directed to investigate the role of PRP with peritoneum in the healing process of experimental Achilles tendon rupture in dogs.

Materials and methods

Healthy local breed dogs (n=18) were randomly allocated into three equal groups (6 animals each). A uniform protocol of general anesthesia consisting of Ketamine 5% (10 mg/kg) and Xylazine 2% (3 mg/kg) intramuscularly (IM) was followed. The site of operation directly over the tendon was prepared under standard sterilization procedures. In the control group, Achilles ten

don was transversely sectioned and repaired with a modified Kessler method only and the leg was fixed with Gipson. In the peritoneal scaffold group, peritoneum graft was harvested directly by making an incision at the lower abdomen near to the umbilicus from the same dog, isolated segment (approximately 3×3 cm) was preserved in ringer solution containing 10% gentamicin. The tendon repaired as mentioned in the control group and augmented with peritoneum graft. In the peritoneal scaffold with the PRP group, the tendon was repaired by tenorrhaphy, augmented with peritoneum graft, and PRP was applied directly on the site of the ruptured area.

The platelet-rich plasma protein (PRP) was prepared at the time of operation where blood samples (20 ml) were collected from the jugular vein and separated into two test tubes (10 ml) containing 0.5 ml of 3.2% sodium citrate. Following centrifugation at 1500 rpm for 10 min, the supernatant aspired and the remaining part of blood represents the PRP (2 ml). This portion was centrifuged again at 1500 rpm for 15 min, then PRP was activated with two drops of 10% calcium chloride (Malik et al., 2013). The site of operation was prepared for surgical operation starting just 5cm proximal to the calcaneus on the lateral aspect of the limb. Then, the surgical site was closed routinely and covered with a non-adhesive dressing bandage. The operated limb immobilized using Gipson (with window) for 2-weeks. Postoperatively, the site of surgery was evaluated clinically at 15, 30, and 60 days. Lameness was categorized according to the lameness scoring (I to VI scale) system (Millis et al., 2004). To determine the gross pathological changes, biopsies were collected from two dogs at each period and the site of the collected specimen was repaired routinely without killing the animal. Ultrasonographic examination was performed at the longitudinal axis (Lamb and Duvernois, 2005). Tissue sections were stained with Harri's hematoxylin and alcoholic eosin (Suvana et al., 2013), and the stained slides were examined at 100X.

Results

Postoperatively, clinical parameters indicated that all operated animals were healthy, alert, and showed normal activity with a good appetite. There was no evidence of serious complications such as infection or wound dehiscence at the operative leg. However, in all groups, animals exhibited lameness a few days post-operation. Lameness was classified according to the lameness score system as grade I. In the control group, the symptoms of lameness persisted for 15 days and 8 days in the peritoneal scaffold group. Interestingly, in the peritoneal scaffold with the PRP group, less severe lameness was reported which lasts for 6 days. Grossly, there was thickening at the area of operation which persisted for 20, 26, and 27 days in control, peritoneal scaffold, and peritoneal scaffold with PRP groups, respectively. In all groups, lameness was subsided gradually. Grossly, in the control group, there was massive adhesion between the tendon and neighboring tissues with incomplete healing at the two ends of the tendon. In the peritoneal scaffold group, there was moderate adhesion with an earlier healing process than the control group (Figure 1). In the peritoneal scaffold with the PRP group, there was mild adhesion with complete healing (Figure 2). Interestingly, in all operated animals, there was no change in the total tendon lenth.

Figure 1

. The peritoneal scaffold group, moderate adhesion with adequate healing (15 days post-surgery).

Figure 2

. The peritoneal scaffold with PRP group mild adhesion with complete healing.

Histopathologically, in the control group, results revealed the presence of maturation of the granulation tissue which character

ized by dense collagen fiber with a moderate proliferation of active fibroblast after 30 days post-surgery. However, after 60 days of operation, mature connective tissue was presented and characterized by the organization of collagen fiber (Figure 3). In the peritoneal scaffold group, at 15 days, there was a severe proliferation of active fibroblasts with a little number of blood vessels. Additionally, there was a reduction in the density of collagen fiber with a mild inflammatory response. At day 60, there was a decrease in the number of spindle fibroblast cells, collagen fiber organization and vascularity were qualitatively similar to those of normal tendon tissue. There were no signs of cartilage or bone formation within the tendon (Figure 4). In the peritoneal scaffold with the PRP group, at 30 days, the presence of connective tissue with collagen fibers formation accompanied by a reduction in the number of fibroblast cells and no inflammatory reaction. At 60 days, sections revealed the presence of new collagen fibers with further decreases in the number of fibroblasts. Besides, edema was noted between collagen fibers (Figure 5).

Figure 3

. Control groups at day 60 post-operation. The section displays the presence of mature connective tissue and the organization of collagen fiber. HandE, 100X.

Figure 4

. The peritoneal scaffold group at 60 days showed a decreased number of spindle fibroblast cells and collagen fiber organization HandE, 100x.

Figure 5

. The peritoneal scaffold with the PRP group at 60 days showed new collagen fibers formation with a decreased number of fibroblast cells. The presence of edema between collagen fibers. HandE, 100X.

In the control group, the sonographic investigation revealed a mottled heterogeneous fiber pattern with an area of hypoechogenicity at 15 days; however, hyperechogenicity was the main feature at 30 days with homogenous fiber pattern (Figure 6). In the peritoneal scaffold group, at 15 days, hyperechogenic with a hypoechogenic area were recognized at the center of the tissue. Moreover, sections showed a small hypoechoic area at 30 days and hyperechogenic at 60 days (Figure 7). In the peritoneal scaffold with the PRP group, at 15 days, the hyperechogenic area was determined at the center. In the 30 and 60 days, there was hyperechogenic hypoechogenicity at the site of operation (Figure 8).

Figure 6

. Longitudinal ultrasound image of a lateral aspect of the calcaneal tendon in the control group at 60 days. Homogenous fiber pattern with an area of hyperechogenic.

Figure 7

. Longitudinal ultrasound image of a lateral aspect of the calcaneal tendon in the peritoneal scaffold group at 60 days. Homogenous fiber pattern with a hyperechoic area.

Figure 8

. Longitudinal ultrasound image of a lateral aspect of the calcaneal tendon in the peritoneal scaffold with the PRP group at 60 days. Homogenous fiber pattern with a smallhypoechogenic area.

Discussion

Tendon regeneration is a complex and very slow process. Several biologic or synthetic scaffold devices for tendon augmentation were used to provide more effective management and increased healing rates (Walden et al., 2016). A successful restoration with a good outcome should have suitable durability, tension, and strength to meet the dynamic workload (Jahani et al., 2015). In the current trial, results showed that treatment with the scaffold of autologous peritoneum has positively accelerated the healing of the ruptured tendon. This outcome might provide evidence that scaffold can serve as temporary supportive materials for the host tissue in the processes of growth and repairing. Furthermore, the using of PRP for augmentation of the transected tendon might provide advantageous effects on the mechanical properties of the tendon. Clinical observation reveals improvement in the gait and gradual decreases of lameness especially at day sex post-surgery in peritoneal scaffold and PRP group. This may be attributed to the role of the peritoneal scaffold as a protective shield, which decreases the adhesion between the tendon and the surrounding region (Castillo et al., 2019). Also, the peritoneal scaffold might have a curative effect due to the proliferation and migration of fibroblasts. For instance, in addition to the extracellular matrix synthesis, rapid degradation of the implanted scaffold was determined; thus, in treated groups, there was an early improvement in the mechanical function of tendon and the signs of lameness subsided rapidly (Bellenger, 2003). Moreover, the addition of PRP acts as a fibrin tissue adhesive, which increases the tensile strength of the tendon and improved gait (Sarrafian et al., 2010). Similarly, a recent study indicated the effective role of using the PRP for repairing digital flexor tendons in rabbits (Sara et al., 2017). Grossly, adhesion is the most important clinical concerns in tendon repair, which is mainly related to unsuccessful functional outcome (Fahie, 2005). The autologous peritoneum scaffold augmented with PRP acts as a protective shield and contribute to overcome adhesion with the neighboring tissue; consequently, keeping the gliding property of the tendon (Kewa et al., 2011; Elenes et al., 2012). By comparison with the control group, the detected degree of adhesion was lesser in the peritoneal scaffold group, which allows to earlier return to the functional activity of the treated leg (Hajipour, 2016).

In all groups, histopathological examination revealed the presence of matured granulation tissue and inflammatory response in the first 15 days with a complete remodeling of injured edges. Besides, there was an extension of the fibrous extracellular matrix between the wound edges; furthermore, a complete maturation of collagen sheets with strength and stretching of wound borders. The previously described processes indicating a completed healing process is evident at the extracellular and cellular levels. The healing process might be enhanced by growth factors that present in PRP; for instance, tumor necrosis factor alfa (Moshiri and Oryan, 2013). Our results in the peritoneal scaffold group demonstrated physiological inflammatory reactions rather than inflammatory processes against pathogens. This observation might be attributed to the positive impact of PRP by in

itiating the healing process through activation of the inflammatory reaction mediating by interleukin-6 (IL-6). Furthermore, the PRP promotes inflammatory reaction by activation of oxygen free radicals that plays an import

ant role in the elimination of pathogens from the contaminated surgical wound (Sample et al., 2018). The effect of PRP might be referred to its content of numerous growth factors including platelet-derived growth factor (PDGF), transforming growth factor-β (TGF-β), vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), insulin-like growth factor (IGF) and fibroblast growth factor (FGF). These factors have the

potency to initiate and accelerate the healing phases through the enhances of angiogenesis, cellular mitosis, and formation of new sheets of collagen fibers (Najafbeygi et al., 2017). In this study, PRP treatment demonstrated complete healing and the affected tissue returned to its normal feature. PRP contains factors, such as IL-6 and IL-12, where these factors found to be influencing the transforming of a tendenocyte into a fibroblast, which is responsible for remolding precursors of collagen fibers into type I collagen fibers (Moshiri and Oryan, 2013). Therefore, our results indicated that regeneration with the using of PRP is much more effective than using peritoneal scaffold alone. The using of PRP along with peritoneal graft might contribute in the remodeling of extracellular matrix components, increase collagen fiber production and deposition, earlier granulation tissue maturation and organization (Cai et al., 2019; Sarafian et al., 2010; Hosgood, 2003).

In all groups, the ultrasonographic examination exhibited thickening of the treated tendon in which continued to be detectable to the end of the study. However, thickening in the control group was much more than the treatment groups, a similar observation was previously reported Fredberg and Bolvig (2002). Another previous work stated that the increased tendon thickness is a consequence of the local inflammation, which is usually accompanied by edema (Rumack et al., 2005). Recent work suggested that the increased tendon size, in both acute and chronic tendinopathies, favor sonography at the affected site. For instance, the increased tendon size in acute tendinitis is a consequence of haemorrhage and edema; however, in chronic tendinitis, the presence of fibrous tissue, intra-tendinous calcification, and degenerative changes, including increased proteoglycan content, loss of collagen organization and bundling, and myxomatous degeneration tend to cause a permanent thickening in the affected tendon (Macdugall et al., 2018).

Sonographic examination in both the control group (15 and 30 days post-surgery) and in the first and second treated group (15 days post-surgery) showed a heterogeneous fiber pattern in the course of the tendon. It has been suggested that the mottled or heterogenous fiber pattern might be associated with several disorders such as fiber disruption, intra-tendinous haemorrhage, disorganization of collagen fibers after surgery (Rumack et al., 2005; Macdugall et al., 2018). Whereas, the improved tendon pattern occurs early (30 days) in the peritoneal scaffold with the PRP group, which indicates that PRP improved the healing process. However, in the peritoneal scaffold group, the inflammation persisted, evident as small hypoechoic areas, even at the 30 days post-surgery. These results are similar to those reported in a previous study specified that the injured Achilles tendon might return to its normal echogenicity after 29 days of treatment (Chamberlain et al., 2013).

The utilizing of peritoneum graft supported with platelets-plasma rich protein (PRP) has a positive impact on acceleration

and improvement of Achilles tendon repair.

Acknowledgments

We would like to thank the College of Veterinary Medicine, Assistant professor Dr. Hana Ismail, Dept. of Pathology; Dr. Isam Sharum for his support during the research period.

 Conflict of Interest

The authors declared that there is no conflict of interest.