Experimental study of the effect of Autologous Platelet Supernatant on the healing of corneal born ulcer in rabbit

Document Type : Original Article

Authors

1 Semnan

2 Graduate, , Faculty of Veterinary Medicine,, Islamic Azad University, Garmsar branch

Abstract

A corneal ulcer is one of the most common eye diseases, which can be caused by trauma and chemical or some microbial agents. This study was carried out to investigate the effects of autologous platelet supernatant (PS) on corneal burn ulcer healing in 30 adult male New Zealand white rabbits. After general anesthesia, alkali wounds were created on the right corneas of rabbits by applying a 6 mm round filter paper, soaked in 1 M NaOH for 60 s. All rabbits were divided into three groups (n=10). In group A, platelet supernatant and in group B, atropine plus ciprofloxacin (AC) eye drops were used (one drop/12 h for 10 days). In group C, rabbits received normal saline, as the control group. Rabbit corneas were collected for histological examination on days 5 and 10. Histopathological factors such as epithelialization, vacuolar changes in epithelium and inflammation were evaluated. According to histopathological findings, a significant difference was observed between the PS group and with two another groups, while no significant difference was found between the AC group and the control group. The results from this study demonstrate that platelet supernatant can significantly promote the healing process of corneal alkali burn in rabbits.
 

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Andrae, J., Gallini, R., Betsholtz, C. 2008. Role of platelet-derived growth factors in physiology and medicine. Genes and Development. 22(10), 1276-1312.
Borzini, P., Mazzucco, L. 2005. Tissue regeneration and in loco administration of platelet derivatives: clinical outcome, heterogeneous products, and heterogeneity of the effector mechanisms. Transfusion. 45, 1759 –1767.
Cooper, D., Chitman, K.D., Williams, M.C., Granger, D.N. 2003. Time-dependent platelet-vessel wall interactions induced by intestinal ischemia-reperfusion. American Journal of Physiology-Gastrointestinal and Liver Physiology. 284(6), 1027-1033.
Dohan Ehrenfest, D.M., Bielecki, T., Mishra, A., Borzini, P., Inchingolo, F., Sammartino, G., Rasmusson, L., Everts, P.A. 2012. In search of a consensus terminology in the field of platelet concentrates for surgical use: platelet-rich plasma (PRP), platelet-rich fibrin (PRF), fibrin gel polymerization and leukocytes. Current Pharmaceutical Biotechnology. 13(7), 1131-1137.
Doucet, C., Ernou, I., Zhang, Y, Llense, J.R., Begot, L., Holy, X., Lataillade, J.J.  2005. Platelet lysates promote mesenchymal stem cell expansion: a safety substitute for animal serum in cell-based therapy applications. Journal of Cellular Physiology. 205, 228–236
Eppley, B.L., Woodell, J.E., Higgins, J. 2004. Platelet quantification and growth factor analysis from platelet-rich plasma: implications for wound healing. Plastic and Reconstructive Surgery. 114, 1502–1508.
Gawaz, M., Langer, H., May, A.E. 2005. Platelets in inflammation and atherogenesis. Journal of Clinical Investigation. 115(12), 3378-3384.
Kuligowski, M.P., Kitching, A.R., Hickey, M.J., 2006. Leukocyte Recruitment to the Inflamed Glomerulus: A Critical Role for Platelet-Derived P-Selectin in the Absence of Rolling. Journal of Immunology. 176 (11), 6991–6999.
Li, Z., Rumbaut, R.E., Burns, A.R., Smith, C.W. 2006. Platelet Response to Corneal Abrasion Is Necessary for Acute Inflammation and Efficient Re-epithelialization. Investigative Ophthalmology & Visual Science. 47(11), 4794-4802.
Li, Z.J., Choi, H-I., Choi. D-K., Sohn, K-C., Im., Seo, Y-J., Lee, Y-H., Lee, J-H., Lee, Y. 2012. Autologous platelet‐rich plasma: a potential therapeutic tool for promoting hair growth. Dermatologic Surgery. 38, 1040‐1046.
Lorenzana-Blanco, N., Santander-García, D., Güell, J.L., Alejandre-Alba N. 2022. Acute management of ocular chemical burns: A review. Journal of EuCornea. 11(3), 1-15.
Nishijima, K., Kiryum J., Tsujikawa, A., Miyamoto, K., Honjo, M., Tanihara, H., Nonaka, A., Yamashiro, K., Katsuta, H., Miyahara, S., Honda, Y., Ogura, Y. 2004. Platelets adhering to the vascular wall mediate postischemic leukocyte-endothelial cell interactions in retinal microcirculation. Investigative Ophthalmology & Visual Science. 45(3), 977-984.
Noroozi Aghideh, A., Kheirandish, M., Abolghasemi, H., Gharehbaghian, A. 2009. Comparison of Cytokine Growth Factors in Platelet Supernatant, Platelet Lysate and Activated Platelet-rich Plasma for Therapeutic Applications. annals of military and health sciences research. 7(3), 149-155.
Pang, K., Du, L., Wu, X. 2010. A rabbit anterior cornea replacement derived from acellular porcine cornea matrix, epithelial cells and keratocytes. Biomaterials. 31(28), 7257-7265.
Pavlovic, V., Ciric, M., Jovanovic, V., Stojanovic, P. 2016. Platelet Rich Plasma: a short overview of certain bioactive components. Open Medicine. 11(1), 242-247.
Reid, B., Song, B., McCaig, C.D., Zhao, M. 2005. Wound healing in rat cornea: the role of electric currents. FASEB Journal. 19(3), 379-86.
Ríos, D.L., López, C., Carmona, J.U. 2015. Evaluation of the anti-inflammatory effects of two platelet-rich gel supernatants in an in vitro system of cartilage inflammation. Cytokine. 76, 505-513.
Sridhar, M.S. 2018. Anatomy of cornea and ocular surface. Indian Journal of Ophthalmology. 66(2), 190-194.
Valeri, C.R., Saleem, B., Ragno, G. 2006. Release of platelet-derived growth factors and proliferation of fibroblasts in the releasates from platelets stored in the liquid state at 22 degrees C after stimulation with agonists. Transfusion. 46, 225–229.
Yang, G., Espandar, L., Mamalis, N., Prestwich, G.D. 2010. A cross-linked hyaluronan gel accelerates healing of corneal epithelial abrasion and alkali burn injuries in rabbits Veterinary Ophthalmology. 13(3), 144–150.