Ferdowsi University of Mashhad

Document Type : Research Articles

Authors

1 Division of Biotechnology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran

2 Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran

3 Department of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran

Abstract

              Immediate intervention with minimal side effects is the most significant factor in the enhancement of wound healing. However, a majority of drugs used for this purpose are chemical-based containing various compounds, such as sulfite, which sometimes causes allergic reactions in a number of patients, or anti-inflammatory agents that cause elevated blood sugar and weight gain. Hence, many researchers look for natural compounds, such as glycoproteins, not only to reduce the side effects but also to improve the speed of healing. In this study, we have created a natural biological dressing using the combination of extracellular matrix  (ECM) derived from articular cartilage and DH5α bacterial ghost (BG). Both articular cartilage and BG contain high amounts of collagen and glycoproteins, and proteoglycans, respectively. The experimental wound on the rabbit pinna was treated by the biological dressing. Then microbial, scanning electron microscopy and microscopic analyses measured the wound healing parameters, including the number of fibroblast cells, the collagen contents, percentage of wound closure, and the number of colonies. The results confirmed ECM (OC), BG (OG) and their mixture (OGC) groups have better effects than control groups. Histological parameters, such as number of fibroblast cells and the amount of collagen fibers, represented a greater degree of wound healing in OGC group compared with OC, OG, and control groups. Our findings proved that ECM and bacterial ghost effectively increased the rate of wound healing. The mixture of ECM and BG provides a biological dressing that could be used in wound repair in the future.

Keywords

 Agyare, C., A. J. Akindele, and V. Steenkamp. 2019. Natural Products and/or Isolated Compounds on Wound Healing. Evid Based Complement Alternat Med 2019:4594965.
Al-Waili, N., K. Salom, and A. A. Al-Ghamdi. 2011. Honey for wound healing, ulcers, and burns; data supporting its use in clinical practice. ScientificWorldJournal 11:766-787.
Barnett, S. E., and S. J. Varley. 1987. The effects of calcium alginate on wound healing. Ann R Coll Surg Engl 69 (4):153-155.
Bitar, M. S. 1997. Insulin-like growth factor-1 reverses diabetes-induced wound healing impairment in rats. Horm Metab Res 29 (8):383-386.
Brigham, P. A., and E. McLoughlin. 1996. Burn incidence and medical care use in the United States: estimates, trends, and data sources. J Burn Care Rehabil 17 (2):95-107.
Broughton, G., 2nd, J. E. Janis, and C. E. Attinger. 2006. Wound healing: an overview. Plast Reconstr Surg 117 (7 Suppl):1e-S-32e-S.
Brouki Milan, P., A. Pazouki, M. T. Joghataei, M. Mozafari, N. Amini, S. Kargozar, M. Amoupour, N. Latifi, and A. Samadikuchaksaraei. 2020. Decellularization and preservation of human skin: A platform for tissue engineering and reconstructive surgery. Methods 171:62-67.
Brown, M., M. K. McDonnell, and D. N. Menton. 1988. Electrical stimulation effects on cutaneous wound healing in rabbits. A follow-up study. Phys Ther 68 (6):955-960.
Caporusso, J., R. Abdo, J. Karr, M. Smith, and A. Anaim. 2019. Clinical experience using a dehydrated amnion/chorion membrane construct for the management of wounds. Wounds 31 (4 Suppl):S19-s27.
Cartmell, J. S., and M. G. Dunn. 2000. Effect of chemical treatments on tendon cellularity and mechanical properties. J Biomed Mater Res 49 (1):134-140.
Gantwerker, E. A., and D. B. Hom. 2011. Skin: histology and physiology of wound healing. Facial Plast Surg Clin North Am 19 (3):441-453.
Ghatak, S., E. V. Maytin, J. A. Mack, V. C. Hascall, I. Atanelishvili, R. Moreno Rodriguez, R. R. Markwald, and S. Misra. 2015. Roles of Proteoglycans and Glycosaminoglycans in Wound Healing and Fibrosis. Int J Cell Biol 2015:834893.
Greaves, N. S., K. J. Ashcroft, M. Baguneid, and A. Bayat. 2013. Current understanding of molecular and cellular mechanisms in fibroplasia and angiogenesis during acute wound healing. J Dermatol Sci 72 (3):206-217.
Hackam, D. J., and H. R. Ford. 2002. Cellular, biochemical, and clinical aspects of wound healing. Surg Infect (Larchmt) 3 Suppl 1:S23-35.
Haidinger, W., U. B. Mayr, M. P. Szostak, S. Resch, and W. Lubitz. 2003. Escherichia coli ghost production by expression of lysis gene E and Staphylococcal nuclease. Appl Environ Microbiol 69 (10):6106-6113.
Hashemzadeh, M. R., N. Mahdavi-Shahri, A. R. Bahrami, M. Kheirabadi, F. Naseri, and M. Atighi. 2015. Use of an in vitro model in tissue engineering to study wound repair and differentiation of blastema tissue from rabbit pinna. In Vitro Cell Dev Biol Anim 51 (7):680-689.
Ibrahim, N., S. K. Wong, I. N. Mohamed, N. Mohamed, K. Y. Chin, S. Ima-Nirwana, and A. N. Shuid. 2018. Wound Healing Properties of Selected Natural Products. Int J Environ Res Public Health 15 (11).
Ji, Y., J. Zhou, T. Sun, K. Tang, Z. Xiong, Z. Ren, S. Yao, K. Chen, F. Yang, F. Zhu, and X. Guo. 2019. Diverse preparation methods for small intestinal submucosa (SIS): Decellularization, components, and structure. J Biomed Mater Res A 107 (3):689-697.
Kapuscinski, J. 1995. DAPI: a DNA-specific fluorescent probe. Biotech Histochem 70 (5):220-233.
Kawano, Y., V. Patrulea, E. Sublet, G. Borchard, T. Iyoda, R. Kageyama, A. Morita, S. Seino, H. Yoshida, O. Jordan, and T. Hanawa. 2021. Wound Healing Promotion by Hyaluronic Acid: Effect of Molecular Weight on Gene Expression and In Vivo Wound Closure. Pharmaceuticals (Basel) 14 (4).
Kumar, P., and G. C. Jagetia. 1995. Modulation of wound healing in Swiss albino mice by different doses of gamma radiation. Burns 21 (3):163-165.
Lubitz, P., U. B. Mayr, and W. Lubitz. 2009. Applications of bacterial ghosts in biomedicine. Adv Exp Med Biol 655:159-170.
Mashreghi, M., M. Rezazade Bazaz, N. Mahdavi Shahri, A. Asoodeh, M. Mashreghi, M. Behnam Rassouli, and S. Golmohammadzadeh. 2013. Topical effects of frog "Rana ridibunda" skin secretions on wound healing and reduction of wound microbial load. J Ethnopharmacol 145 (3):793-797.
Park, M., S. Kim, I. S. Kim, and D. Son. 2008. Healing of a porcine burn wound dressed with human and bovine amniotic membranes. Wound Repair Regen 16 (4):520-528.
Paukner, S., T. Stiedl, P. Kudela, J. Bizik, F. Al Laham, and W. Lubitz. 2006. Bacterial ghosts as a novel advanced targeting system for drug and DNA delivery. Expert Opin Drug Deliv 3 (1):11-22.
Piccoli, M., C. Trevisan, E. Maghin, C. Franzin, and M. Pozzobon. 2018. Mouse Skeletal Muscle Decellularization. Methods Mol Biol 1577:87-93.
Reddy, K. K., L. Grossman, and G. S. Rogers. 2013. Common complementary and alternative therapies with potential use in dermatologic surgery: risks and benefits. J Am Acad Dermatol 68 (4):e127-e135.
Schallberger, S. P., B. J. Stanley, J. G. Hauptman, and B. A. Steficek. 2008. Effect of porcine small intestinal submucosa on acute full-thickness wounds in dogs. Vet Surg 37 (6):515-524.
Shirakigawa, N., and H. Ijima. 2018. Decellularization of Liver and Organogenesis in Rats. Methods Mol Biol 1577:271-281.
Soleymani, S., A. Tavassoli, G. Hashemi Tabar, G. A. Kalidari, and H. Dehghani. 2020. Design, development, and evaluation of the efficacy of a nucleic acid-free version of a bacterial ghost candidate vaccine against avian pathogenic E. coli (APEC) O78:K80 serotype. Vet Res 51 (1):144.
Stanford, W., B. W. Rappole, and C. L. Fox, Jr. 1969. Clinical experience with silver sulfadiazine, a new topical agent for control of pseudomonas infections in burns. J Trauma 9 (5):377-388.
Velnar, T., T. Bailey, and V. Smrkolj. 2009. The wound healing process: an overview of the cellular and molecular mechanisms. J Int Med Res 37 (5):1528-1542.
CAPTCHA Image