Role of Semax and Selank neuropeptides in modulating cell-mediated immunity in the setting of skin burn injury

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Abstract

Relevance. The work describes the results of neuropeptide compounds Semax and Selank in modulating disorders of the cellular link of immunity under experimental burn exposure. The aim — to study the effect of Semax and Selank on the number of white blood cells and phagocytic activity of neutrophils of white rats under experimental burn exposure. Materials and Methods. Burn injury in male rats of 6–8 months of age was modeled by expo animals; animals exposed to burns and not treated burn-exposed animals treated with Semax; animals exposed to burn and treated with Selank. Neuropeptide injections at 100 μg/kg/day were performed intraperitoneally daily for 14 days from thermal burn simulation. To study the immunity parameters, the number of white blood cells and the percentage of lymphocytes, rod and segmented neutrophils were calculated, and the phagocytic activity of neutrophils was assessed. Results and Discussion. It was established that under the conditions of experimental burn exposure, there is an increase in the parameters of the cellular link of immunity: phagocytic activity of neutrophils, phagocytic index, phagocytic number, leukocytic coefficient and number of leukocytes. The activation of granulocyte formation was evidenced by an increase in the rod-nucleating forms of leukocytes (shift of the leukocyte formula to the left). Intraperitoneal injections of the neuropeptide drugs Semax and Selank against the background of thermal skin injury contributed to the correction of the observed changes in white blood parameters and functional neutrophil activity. Conclusion. Thus, under the conditions of a skin burn wound with the use of neuropeptide compounds Semax and Selank, dysfunctional transformations of immunocompetent cells are restored, which confirms the complex effect of Semax and Selank on systemic disorders against the background of local stress, namely, the manifestation.

About the authors

Alfiya K. Azhikova

Astrakhan State Medical University

Author for correspondence.
Email: alfia-imacheva@mail.ru
ORCID iD: 0000-0001-9758-1638
SPIN-code: 1245-3158
Astrakhan, Russian Federation

Marina A. Samotrueva

Astrakhan State Medical University

Email: alfia-imacheva@mail.ru
ORCID iD: 0000-0001-5336-4455
SPIN-code: 5918-1341
Astrakhan, Russian Federation

Lyudmila A. Andreeva

Kurchatov Institute, Institute of Molecular Genetics

Email: alfia-imacheva@mail.ru
ORCID iD: 0000-0002-3927-8590
SPIN-code: 4785-5621
Moscow, Russian Federation

Nikolay F. Myasoedov

Kurchatov Institute, Institute of Molecular Genetics

Email: alfia-imacheva@mail.ru
ORCID iD: 0000-0003-4168-4851
SPIN-code: 1262-2698
Moscow, Russian Federation

References

  1. Belokhvostova D, Berzanskyte I, Cujba AM, Jowett G, Marshall L, Prueller J, Watt FM. Homeostasis, regeneration and tumour formation in the mammalian epidermis. Int J. Dev Biol. 2018;62(6–7–8):571–582. (In Russian).
  2. Khaitov RM. Immunology: structure and function of immune system. Textbook. 2nd, renewed. Moscow: GEOTAR-Media; 2019. 328 p. (In Russian).
  3. Samotrueva MA, Yasenyavskaya AL, Tsibizova АA, Bashkina OA, Galimzyanov KhM, Tyurenkov IN. Neuroimmunoendocrinology: modern concepts of molecular mechanisms. Immunology.2017;38(1):49–59. doi: 10.18821/0206–4952–2017–38–1–49–59. (In Russian).
  4. Voisin T, Bouvier A, Chiu IM. Neuro-immune interactions in allergic diseases: novel targets for therapeutics. Int Immunol.2017;29(6):247–261. doi: https://doi: 10.1093/intimm/dxx040
  5. Makhneva NV. Cellular and humoral components of the skin immune system. Russian magazine of skin and venereal diseases.2016;19(1):12–17. (In Russian).
  6. Kon’kov SV, Ilyukevich GV, Zolotukhina LV. Evaluation of the effectiveness of the immunocorrection method in patients with severe thermal trauma. Emergency medicine.2016;5(1):72–79. (In Russian).
  7. Korneva EA., Shanin SN, Novikova NS et al. Cell-molecular bases of neuroimmune interaction under stress. Russian physiological journal named after I.M. Sechenov.2017;103(3):217–229. (In Russian).
  8. Morrison VV, Bozhedomov AYu, Simonyan MA, Morrison AV. Systemic inflammatory response and cytokine profile in the dynamics of burn disease. Saratov Scientific and Medical Journal.2017;13(2):229–232. (In Russian).
  9. Veiga-F ernandes H, Mucida D. Neuro-I mmune Interactions at Barrier Surfaces.Cell.2016;165(4):801–811. doi:10.1016/j. cell.2016.04.041
  10. Vinaik R, Abdullahi A, Barayan D, Jeschke MG. NLRP3 inflammasome activity is required for wound healing after burns. Transl Res.2020;217:47–60. doi: 10.1016/j.trsl.2019.11.002.
  11. Abo El-N oor MM, Elgazzar FM, Alshenawy HA. Role of inducible nitric oxide synthase and interleukin-6 expression in estimation of skin burn age and vitality. J Forensic Leg Med.2017;52:148–153. doi: 10.1016/j.jflm.2017.09.001.
  12. Oka T, Ohta K, Kanazawa T, Nakamura K. Interaction between Macrophages and Fibroblasts during Wound Healing of Burn Injuries in Rats. Kurume Med J.2016; 62(3–4):59–66.doi: 10.2739/kurumemedj. MS00003
  13. Farinas AF, Bamba R, Pollins AC, Cardwell NL, Nanney LB, Thayer WP. Burn wounds in the young versus the aged patient display differential immunological responses. Burns. 2018;44(6):1475–1481. doi: 10.1016/j.burns.2018.05.012
  14. El Khatib A, Jeschke MG. Contemporary Aspects of Burn Care. Medicina (Kaunas).2021;57(4):386. doi: 10.3390/medicina57040386
  15. George B, Suchithra TV, Bhatia N. Burn injury induces elevated inflammatory traffic: the role of NF-κB. Inflamm Res. 2021;70(1):51–65. doi: 10.1007/s00011–020–01426-x
  16. Jeschke MG, van Baar ME, Choudhry MA, Chung KK, Gibran NS, Logsetty S. Burn injury. Nat Rev Dis Primers. 2020;6(1):11. doi: 10.1038/s41572–020–0145–5
  17. Moins-T eisserenc H, Cordeiro DJ, Audigier V, Ressaire Q, Benyamina M, Lambert J, Maki G, Homyrda L, Toubert A, Legrand M. Severe Altered Immune Status After Burn Injury Is Associated With Bacterial Infection and Septic Shock. Front Immunol. 2021;12:586195. doi: 10.3389/fimmu.2021.586195
  18. Burns B, Jackson K, Farinas A, Pollins A, Bellan L, Perdikis G, Kassis S, Thayer W. Eosinophil infiltration of burn wounds in young and older burn patients. Burns.2020;46(5):1136–1141. doi: 10.1016/j. burns.2019.11.022
  19. Jackson KR, Pollins AC, Assi PE, Kassis SK, Cardwell NL, Thayer WP. Eosinophilic recruitment in thermally injured older animals is associated with worse outcomes and higher conversion to full thickness burn. Burns. 2020;46(5):1114–1119. doi:10.1016/j. burns.2019.10.018
  20. Willis ML, Mahung C, Wallet SM, Barnett A, Cairns BA, Coleman LGJr, Maile R. Plasma extracellular vesicles released after severe burn injury modulate macrophage phenotype and function. J Leukoc Biol. 2022;111(1):33–49. doi: 10.1002/JLB.3MIA0321–150RR
  21. Azhikova AK., Yasenyavskaya AL, Samotrueva MA. Immune reactivity features in post-burn dynamics. RUDN Journal of Medicine. 2022; 26(2):194–202. doi: 10.22363/2313–0245–2022–26–2–194–202. (In Russian).

Supplementary files

Supplementary Files
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1. Fig. 1. Total Number of White Blood Cells of Influence in Background, Burn Injury, and Neuropeptide Treatment with Semax and Selank

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2. Fig. 2. Value of leukocytic coefficient of Influence in Background, Burn Injury, and Neuropeptide Treatment with Semax and Selank

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Copyright (c) 2024 Azhikova A.K., Samotrueva M.A., Andreeva L.A., Myasoedov N.F.

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

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