Macroscopic and sonographic correlations in the assessment of burn injury regeneration in guinea pig skin under the influence of the secretome of multipotent mesenchymal stromal cells

Authors

DOI:

https://doi.org/10.31279/2949-4796-2026-16-1-69-81

Keywords:

skin, ultrasound, MMSC secretome, thermal skin burns in animals, regeneration

Abstract

Introduction. Thermal skin burns in farm animals represent a common traumatic injury, leading to culling, reduced productivity, and significant economic losses. Existing treatment modalities in veterinary practice are often insufficiently effective due to delayed wound debridement, infection, and extensive scarring. Stimulation of repair to improve treatment outcomes is achievable through the use of regenerative agents, particularly the secretome of multipotent mesenchymal stromal cells (MMSCs), which contains a complex of cytokines with both pro- and anti-inflammatory activity.
Aim. To evaluate the effect of the MMSC secretome on skin repair following a third-degree thermal burn.
Materials and methods. The study was conducted on 60 guinea pigs. A third-degree thermal burn was simulated on the femoral skin, after which the animals were divided into a control group (saline solution, n=20), an experimental group (MMSC secretome, n=20), and a comparison group (dexpanthenol-based ointment, n=20). Examinations were performed on days 7, 30, and 60, employing a comprehensive methodological approach that included clinical observation, ultrasonographic, and histological studies.
Results. The study demonstrates that the MMSC secretome stimulates macrophage-mediated resorption of detritus, as well as neoangiogenesis, granulation tissue formation, and epithelialization at the early stage (day 7). By day 30, the experimental group exhibited earlier maturation of fibrous tissue and the appearance of signs of organotypic structure in the peripheral parts of the regenerate, compared to the other groups. On day 60, scar changes in the skin were minimal compared to the control and comparison groups. At this stage, the smaller central area of the regenerate was represented by a normotrophic scar with signs of remodeling, while the peripheral area exhibited an organotypic structure.
Conclusion. The application of the MMSC secretome stimulates reparative regeneration of skin after a thermal burn by promoting rapid detritus resorption, enhancing granulation tissue growth, and facilitating the maturation and remodeling of scar tissue, with a pronounced tendency towards the formation of an organotypic regenerate. The obtained data substantiate the feasibility of further studies in farm animals and the development of veterinary drugs based on the secretome.

To cite: Usacheva A.A., Borkhunova E.N., Kuznetsova M.A., Dovgii A.I. Macroscopic and sonographic correlations in the assessment of burn injury regeneration in guinea pig skin under the influence of the secretome of multipotent mesenchymal stromal cells. Agrarian Bulletin of the North Caucasus. 2026;16(1):69-81. (In Russ.) https://doi.org/10.31279/2949-4796-2026-16-1-69-81 

References

Chmielowiec-Korzeniowska A., Nowakowicz-Dębek B., Bis-Wencel H., et al. Safety of animals on livestock farms during a fire emergency. Animal Science and Genetics. 2025;21(1):1–9. https://doi.org/10.5604/01.3001.0055.0463

Bolcato M., Rocarro M., Gentile A., et al. First report on medical treatment and outcome of burnt cattle. Veterinary Sciences. 2023;10(3):187. https://doi.org/10.3390/vetsci10030187

Chigerwe M., Depenbrock S.M., Heller M.C., et al. Clinical management and outcomes for goats, sheep, and pigs hospitalized for treatment of burn injuries sustained in wildfires: 28 Cases (2006, 2015, and 2018). Journal of the American Veterinary Medical Association. 2020;257(11):1165–1170. https://doi.org/10.2460/javma.257.11.1165

Zinoviev E.V., Soloshenko V.V., Kostyakov D.V. et al. Prediction of the outcome of skin grafting based on microcirculation parameters in a burn wound. Russian Sklifosovsky Journal of Emergency Medical Care. 2022;11(3):412-418. (In Russ.) https://doi.org/10.23934/2223-9022-2022-11-3-412-418

Shtykhno Y.M., Udovichenko V.I. Comparative study of intravital microcirculation and blood rheology in rats after burns of different degrees of severity. Bulletin of Experimental Biology and Medicine. 1979;88:984–986. https://doi.org/10.1007/BF00799260

Vizoso F.J., Eiro N., Cid S. et al. Mesenchymal stem cell secretome: Toward cell free therapeutic strategies in regenerative medicine. International Journal of Molecular Sciences. 2017;18(9):1852. https://doi.org/10.3390/ijms18091852

Fedorova A.O., Aistova L.G., Miller T.V. et al. Pathomorphological characteristics of burn disease in rabbits under non-invasive electromagnetic therapy. Bulletin of KrasSAU. 2025;(9(222)):215-228. (In Russ.) https://doi.org/10.36718/1819-4036-2025-9-215-228

Kuznetsova M.A., Borkhunova E.N., Stepanishin V.V., Pozyabin S.V. Possibilities of using MMSC secretome to stimulate osteoreparation: an experimental study. Veterinaria i Kormlenie. 2025;(1):48-53. (In Russ.) https://doi.org/10.30917/ATT-VK-1814-9588-2025-1-10

Saroyan S.V., Komarov S.V. Evaluation of the effectiveness of using mesenchymal stem cell secretome in the postoperative therapy of corneal sequestrum. Systematization of clinical experience. Scientific Notes of the Kazan Bauman State Academy of Veterinary Medicine. 2021;(4):196–203. (In Russ.) https://doi.org/10.31588/2413-4201-1883-248-4-196-203

Kangari P., Talaei-Khozani T., Razeghian Jahromi I. et al. Mesenchymal stem cells: amazing remedies for bone and cartilage defects. Stem Cell Research & Therapy. 2020;11(1):492. https://doi.org/10.1186/s13287-020-02001-1

L P.K., Kandoi S., Misra R. et al. The mesenchymal stem cell secretome: A new paradigm towards cell-free therapeutic mode in regenerative medicine. Cytokine & Growth Factor Reviews. 2019;46:1–9. https://doi.org/10.1016/j.cytogfr.2019.04.002

Kachalin M.D., Borkhunova E.N., Pozyabin S.V. et al. Reparative regeneration of tendon under the influence of the secretome of multipotent mesenchymal stromal cells: an experimental study. Clinical and Experimental Morphology. 2023;12(2):77–88. (In Russ.) https://doi.org/10.31088/CEM2023.12.2.77-88

Maiborodin I.V., Shevela A.I., Morozov V.V. et al. Influence of extracellular vesicles (exosomes) of mesenchymal stromal cells on bone tissue regeneration. Novosti Khirurgii. 2019;(2). (In Russ.) https://doi.org/10.18484/2305-0047.2019.2.196

Lee K.C., Dretzke J., Grover L., Logan A., Moiemen N. A systematic review of objective burn scar measurements. Burns & Trauma. 2016;4:14. https://doi.org/10.1186/s41038-016-0036-x

Seidenari S., Giusti G., Bertoni L., Magnoni C., Pellacani G. Thickness and echogenicity of the skin in children as assessed by 20-MHz ultrasound. Dermatology. 2000;201(3):218–222. https://doi.org/10.1159/000018491

Wang X-Q., Mill J., Kravchuk O., Kimble R.M. Ultrasound assessed thickness of burn scars in association with laser Doppler imaging determined depth of burns in paediatric patients. Burns. 2010;36(8):1254–1262. https://doi.org/10.1016/j.burns.2010.05.01

Lau J.C., Li-Tsang C.W., Zheng Y.P. Application of tissue ultrasound palpation system (TUPS) in objective scar evaluation. Burns. 2005;31(4):445–452. https://doi.org/10.1016/j.burns.2004.07.016

Hambleton J., Shakespeare P.G., Pratt B.J. The progress of hypertrophic scars monitored by ultrasound measurements of thickness. Burns. 1992;18(4):301–307. https://doi.org/10.1016/0305-4179(92)90151-j

Simons M., Kee E.G., Kimble R., Tyack Z. Ultrasound is a reproducible and valid tool for measuring scar height in children with burn scars: a cross-sectional study of the psychometric properties and utility of the ultrasound and 3D camera. Burns. 2017;43(5):993–1001. https://doi.org/10.1016/j.burns.2017.01.034

Sokolov A.A., Kolesnikova A.I., Dovgiy A.I. et al. Patent № 2708329 C2, Russian Federation. Stem cell material, compositions and methods of use. № 2016121458: filed on 31.05.2016 published on 11.01.2024, applicant T-Helper cell technologies (In Russ.)

Singer A.J., McClain S.A. A porcine burn model. In: DiPietro L.A., Burns A.L., editors. Methods in Molecular Medicine, Vol. 78: Wound Healing: Methods and Protocols. Totowa, New Jersey: Humana Press Inc.; 2003. p. 107-119. https://doi.org/10.1385/1-59259-332-1:107

How to Cite

Usacheva А., Borkhunova Е., Kuznetsova М., & Dovgii А. (2026). Macroscopic and sonographic correlations in the assessment of burn injury regeneration in guinea pig skin under the influence of the secretome of multipotent mesenchymal stromal cells. Agrarian Bulletin of the North Caucasus, 16(1), 69–81. https://doi.org/10.31279/2949-4796-2026-16-1-69-81

Issue

Section

Animal Husbandry and Veterinary Medicine