Iranian Journal of Veterinary Surgery

Iranian Journal of Veterinary Surgery

Evaluation of Potential Effect of Bone Marrow Mast Cells on Burn Wound Healing in Rat

Document Type : Original Article

Authors
1 Department of Pathology, Faculty of Veterinary Medicine, Urmia Branch, Islamic Azad University, Urmia, Iran.
2 Department of Surgery and Diagnostic Imaging, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Abstract
The objective of this work was to assess the potential effect of bone marrow mast cells (BMMCs) on burn wound healing in rats. We included 45 male rats into three groups of 15 animals each: CNTRL group: We treated the burn wounds with normal saline (0.1 ml). TRTMENT group: In this group, the burn wounds were treated with bone marrow mast cells (1× 106/ml). SSD (Positive control) group: In this group, the wounds were treated with silver sulfadiazine 1% ointment. Wound area reduction measurements, histopathological studies, and biochemical assessments levels showed significant differences between rats in TRTMENT group in comparison with other groups (p < 0.05). Accelerated repair of the wounds in TRTMENT group showed that local application of BMMCs could be taken into consideration in burn wound healing.
Keywords

Subjects


  1. Jeschke MG, van Baar ME, Choudhry, M A, Chung K K, Gibran N S, Logsetty, S. Burn injury. Nature Reviews. Disease Primers. 2020: 6(1): 11. doi: 10.1038/s41572-020-0145-5
  2. Stone IR, Natesan S, Kowalczewski CJ, Mangum LH, Clay NE, Clohessy RM, Carlsson AH, Tassin, DH, Chan RK, Rizzo JA, Christy RJ. Advancements in regenerative strategies through the continuum of burn care. Frontiers in Pharmacology. 2018; 9: 672. doi: 10.3389/fphar.2018.00672
  3. Leclerc T, Thepenier C, Jault P, Bey E, Peltzer J, Trouillas M, Duhamel P, Bargues L, Prat M, Bonderriter M, Lataillade JJ. Cell therapy of burns. Cell Proliferation. 2011; 44 (Suppl 1): 48–54. doi: 10.1111/j.1365-2184.2010.00727.x
  4. Zhang X, Xing H, Zhao Y, Ma Z. Pharmaceutical dispersion techniques for dissolution and bioavailability enhancement of poorly water-soluble drugs. Pharmaceutics. 2018; 10(3): 74. doi: 10.3390/pharmaceutics10030074
  5. Carsin H, Ainaud P, Le Bever H, Rives J, Lakhel A, Stephanazzi J, Lambert F, Perrot J. Cultured epithelial autografts in extensive burn coverage of severely traumatized patients: a five year single‐center experience with 30 patients. Burns. 2000; 26: 379–387. doi: 10.1016/s0305-4179(99)00143-6
  6. Srivastava S, Mishra S, Dewangan J, Divakar A, Gupta N, Kalleti N, Mugale MN, Kumar S, Sharma S, Rath SK. Safety assessment of the pharmacological excipient, diethylene glycol monoethyl ether (DEGEE), using in vitro and in vivo systems. Daru. 2019; 27(1): 219–231. doi: 10.1007/s40199-019-00264-5
  7. van Eeden CM, Liebenberg W, du Preez JL, de Villiers MM. Solvent and surfactant enhanced solubilization, stabilization, and degradation of amitraz. Journal of environmental science and health. Part. B, Pesticides, Food Contaminants, and Agricultural Wastes. 2044; 39(1): 33–51. doi: 10.1081/pfc-120027437
  8.  Singhal M, Baumgartner A, Turunen E, van Veen B, Hirvonen J, Peltonen L. Nanosuspensions of a poorly soluble investigational molecule ODM-106: Impact of milling bead diameter and stabilizer concentration. International Journal of Pharmaceutics. 2020; 587: 119636. doi: 10.1016/j.ijpharm.2020.119636
  9.  Ahmadi Tehrani A, Omranpoor MM, Vatanara A, Seyedabadi M, Ramezani V. Formation of nanosuspensions in bottom-up approach: theories and optimization. Daru. 2019; 27(1): 451–473. doi: 10.1007/s40199-018-00235-2
  10. Zhao M, Lee SH, Song JG, Kim HY, Han HK. Enhanced oral absorption of sorafenib via the layer-by-layer deposition of a pH-sensitive polymer and glycol chitosan on the liposome. International Journal of Pharmaceutic.  2018; 544(1): 14–20. doi: 10.1016/j.ijpharm.2018.04.020
  11. Kato Y, Onishi H, Machida,Y. Application of chitin and chitosan derivatives in the pharmaceutical field. Current Pharmaceutical Biotechnology. 2003; 4(5): 303–309. doi: 10.2174/1389201033489748
  12.  Brey Gil VS, Brey Gil CS, Goulart G, Oréfice RL. Multi-drug hybrid delivery systems with distinct release profiles based on gelatin/collagen containing vesicles derived from block copolymers. International Journal of Biological Macromolecules. 2019; 139: 967–974. doi: 10.1016/j.ijbiomac.2019.08.056
  13. Sadeghinia A, Soltani S, Aghazadeh M, Khalilifard J, Davaran, S. Design and fabrication of clinoptilolite-nanohydroxyapatite/chitosan-gelatin composite scaffold and evaluation of its effects on bone tissue engineering. Journal of Biomedical Materials Research. Part A. 2020; 108(2): 221–233. doi: 10.1002/jbm.a.36806
  14. Cheng YH, Ko YC, Chang YF, Huang SH, Liu CJ. Thermosensitive chitosan-gelatin-based hydrogel containing curcumin-loaded nanoparticles and latanoprost as a dual-drug delivery system for glaucoma treatment. Experimental Eye Research. 2019; 179: 179–187. doi: 10.1016/j.exer.2018.11.017
  15. Farnia P, Mollaei, S , Bahrami A, Ghassempour A, Velayati AA, Ghanavi J. Improvement of curcumin solubility by polyethylene glycol/chitosan-gelatin nanoparticles (CUR-PEG/CS-G-nps). Biomedical Research. 2016; 27 (3): 659-665.
  16. Bamrungsap S, Zhao Z, Chen T, Wang L, Li C, Fu T, Tan W. Nanotechnology in therapeutics: a focus on nanoparticles as a drug delivery system. Nanomedicine. 2012; 7(8): 1253–1271. doi: 10.2217/nnm.12.87
  17. Qiu Z, Kwon AH, Kamiyama Y. Effects of plasma fibronectin on the healing of full-thickness skin wounds in streptozotocin-induced diabetic rats. The Journal of Surgical Research. 2007; 138(1): 64–70. doi: 10.1016/j.jss.2006.06.034
  18. Taghavifar S, Afroughi F,Saadati Keyvan M. Curcumin nanoparticles improved diabetic wounds infected with methicillin-resistant Staphylococcus aureus sensitized with HAMLET. The International Journal of Lower Extremity Wounds. 2022; 21(2): 141-153. doi: 10.1177/1534734620933079
  19. Guo S, Fang Q, Chen L, Yu M, Chen Y, Li N, Han C, Hu X. Locally activated mitophagy contributes to a "built-in" protection against early burn-wound progression in rats. Life Sciences. 2021; 276: 119095. doi: 10.1016/j.lfs.2021.119095
  20. Kassem A, Ayoub GM, Malaeb L. Antibacterial activity of chitosan nano-composites and carbon nanotubes: a review. The Science of the Total Environment. 2019; 668: 566–576. doi: 10.1016/j.scitotenv.2019.02.446
  21. Stoica AE, Chircov C, Grumezescu AM. Nanomaterials for wound dressings: an up-to-date overview. Molecules. 2020; 25(11): 2699. doi: 10.3390/molecules25112699
  22. Kallel I, Hadrich B, Gargouri B, Chaabane A, Lassoued S, Gdoura R, Bayoudh A, Ben Messaoud E. Optimization of cinnamon (Cinnamomum zeylanicum blume) essential oil extraction: evaluation of antioxidant and antiproliferative effects. Evidence-Based Complementary and Alternative Medicine: eCAM. 2019, 6498347. doi: 10.1155/2019/6498347
  23. Thangapazham RL, Sharad S, Maheshwari RK. Skin regenerative potentials of curcumin. BioFactors. 2013; 39(1): 141–149. doi: 10.1002/biof.1078
  24. Aziz Z, Abdul Rasool Hassan B. The effects of honey compared to silver sulfadiazine for the treatment of burns: a systematic review of randomized controlled trials. Burns. 2017; 43(1): 50–57. doi: 10.1016/j.burns.2016.07.004
  25. Patrulea V, Ostafe V, Borchard G, Jordan O. Chitosan as a starting material for wound healing applications. European Journal of Pharmaceutics and Biopharmaceutics. 2015; 97(Pt B): 417–426. doi: 10.1016/j.ejpb.2015.08.004
  26. Diegelmann RF, Evans MC. Wound healing: an overview of acute, fibrotic and delayed healing. Frontiers in Bioscience. 2004; 9: 283–289. doi: 10.2741/1184
  27. Marchete R, Oliveira S, Bagne L, Silva JIS, Valverde AP, Aro AA, Figueira MM, Fronza M, Bressam TM, Goes VFF, Gaspari de Gaspi FO, Dos Santos GMT, Andrade TAM. Anti-inflammatory and antioxidant properties of Alternanthera brasiliana improve cutaneous wound healing in rats. Inflammopharmacology. 2021; 29(5): 1443–1458. doi: 10.1007/s10787-021-00862-3
  28. Chen D, Hao H, Fu X, Han W. Insight into reepithelialization: how do mesenchymal stem cells perform? Stem Cells International. 2016; 2016: 6120173. doi: 10.1155/2016/6120173
  29. Samdavid Thanapaul R, Ranjan A, Manikandan SK, Nadar M. Efficacy of Lobelia alsinoides Lam ethanolic extract on a third-degree burn: An experimental study on rats. Dermatologic Therapy. 2020; 33(6): e14242. doi: 10.1111/dth.14242
  30. Ladhani HA, Yowler CJ, Claridge JA. Burn wound colonization, infection, and sepsis. Surgical Infections. 2021; 22(1): 44–48. doi: 10.1089/sur.2020.346
  31.  Gibson-Corley KN, Olivier AK, Meyerholz,D K. Principles for valid histopathologic scoring in research. Veterinary Pathology. 2013; 50(6): 1007–1015. doi: 10.1177/0300985813485099

  • Receive Date 04 March 2024
  • Revise Date 14 May 2024
  • Accept Date 18 May 2024
  • First Publish Date 18 May 2024