Korman Sh.-A. S., Lukyantseva H. V.
ULTRASTRUCTURAL PROFILE OF SKELETAL MUSCLE ADAPTATION TO PHYSICAL LOAD UNDER CONDITIONS OF TRAINING
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About the author:
Korman Sh.-A. S., Lukyantseva H. V.
Heading:
MORPHOLOGY
Type of article:
Scientific article
Annotation:
Physical exercise induces a multilevel adaptation of skeletal muscle tissue, involving both functional and ultrastructural components. The mitochondrial apparatus, microcirculatory network, and blood–tissue (histohistological) barrier play a central role in these adaptive processes. Investigating the differences in response between trained and untrained organisms allows for identification of the morphological reserve mechanisms that determine skeletal muscle resistance to hypoxic stress. A comparative analysis at the subcellular level helps to elucidate both compensatory and destructive shifts. Aim is to investigate the ultrastructural mechanisms of skeletal muscle adaptation to graded physical load depending on the degree of training in rats. The study was conducted on sexually mature male Wistar rats, divided into control, untrained, and trained groups (daily swimming for 30 days). After graded physical loading (GPL), morphometric analysis of the gastrocnemius muscle and myocardium was performed using transmission electron microscopy. Trained rats demonstrated an increase in the number of functioning capillaries, expansion of the mitochondrial pool, preservation of microcirculatory structure, and reduced edema following GPL. In contrast, untrained animals exhibited destructive changes such as organelle vacuolization, histohistological barrier hyperhydration, impaired oxygen diffusion, and disrupted energy supply. Regular training promotes structural stability of skeletal muscle and facilitates the formation of an adaptive reserve that enhances resistance to physiological stress.
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Bibliography:
- Coletti C, Acosta GF, Keslacy S, Coletti D. Exercise-mediated reinnervation of skeletal muscle in elderly people: An update. Eur J Transl Myol. 2022;32(1):10416. DOI: 10.4081/ejtm.2022.10416.
- Pepper I, Galkin VE. Actomyosin Complex. Subcell Biochem. 2022;99:421-470. DOI: 10.1007/978-3-031-00793-4_14.
- Pastukhova V, Lukyjantseva H, Dudenko V. Strukturnaja perestrojka skeletnyh myshc pod vozdejstviem dlitelnyh fizicheskih nagruzok. Eksper. Klin. Med. 2014;63(2):118-22.
- Gan Z, Fu T, Kelly DP, Vega RB. Skeletal muscle mitochondrial remodeling in exercise and diseases. Cell Res. 2018;28(10):969-980.
- Poole DC, Behnke BJ, Musch TI. The role of vascular function on exercise capacity in health and disease. J Physiol. 2021;599(3):889-910.
- Gaffney K, Lucero A, Macartney-Coxson D, Clapham J, Whitfield P, Palmer BR, et al. Effects of whey protein on skeletal muscle microvascular and mitochondrial plasticity following 10 weeks of exercise training in men with type 2 diabetes. Appl Physiol Nutr Metab. 2021;46(8):915-924.
- Perry CGR. Mitochondrial adaptations to exercise in human skeletal muscle: a possible role for cristae density as a determinant of muscle fitness. J Physiol. 2017;595(9):2773-2774. DOI: 10.1113/JP273549.
- Malyuha SS, Lukyantseva HV, Bakunovskyi O M. Osoblyvosti roboty sertsia i hemodynamiky u period vidnovlennia pislia stato- dynamichnoho fizychnoho navantazhennia. Visn. Probl. Biol. Med. 2022;3(166):482-91. DOI: 10.29254/2077-4214-2022-3-166-482-491. [in Ukrainian].
- Malyuga SS, Lukyantseva HV, Bakunovsky OO. Features of functional changes in blood vessels during the period of early recovery after static physical exercise. Rep. Morphol. 2022;28(4):48-53. DOI: 10.31393/ morphology-journal-2022-28(4)-07.
- Lopes KG, Farinatti P, Bottino DA, de Souza MDGC, Maranhão PA, Bouskela E, et al. Sarcopenia in the elderly versus microcirculation, inflammation status, and oxidative stress: A cross-sectional study. Clin Hemorheol Microcirc. 2022;80(2):185-195. DOI: 10.3233/CH-211202.
- Law M, Wang PC, Zhou ZY, Wang Y. From Microcirculation to Aging-Related Diseases: A Focus on Endothelial SIRT1. Pharmaceuticals (Basel). 2024;17(11):1495. DOI: 10.3390/ph17111495.
- Weakley BS. A Beginner`s Handbook in Electron Microscopy. Edinburg, London: Churchill Livingstone; 1972. 228 p.
- Weibel ER. Stereological principles for morphometry in electron microscopic cytology. Int Rev Cytol. 1969;26(2):235-302.
- Hoppler H, Vogt M. Muscle tissue adaptation to hypoxia. J. Experim. Biol. 2001;204(18):3133-9.
- Weibel ER. Human lung morphometry. Berlin, Heidelberg: Springer; 1970. 176 p.
- Pokotylo PB. Ultrastrukturne doslidzhennia mitokhondrial’noho aparatu kardiomiotsytiv intaktnykh shchuriv. Svit Med. Biol. 2014;21(5):148- 51. [in Ukrainian].
- Rozova KV, Tymoshenko KR, Viunytskyi VP, Bielikova MV, Sydoriak NH. Osoblyvosti strukturnykh zmin u tkanyni lytkovoho miaza ta miokardi i pokaznykiv mikrotsyrkuliatsii krovi pry dozovanomu fizychnomu navantazhenni u tvaryn z riznym stupenem trenovanosti. Fiziol. zhurn. 2019;65(4):20-30. [in Ukrainian].
- Santos JD, Paulo M, Vercesi JA, Bendhack LM. Thromboxane-prostanoid receptor activation blocks ATP-sensitive potassium channels in rat aortas. Clin Exp Pharmacol Physiol. 2021;48(11):1537-46.
- Ahmadian M, Erskine E, Wainman L, Wearing OH, Duffy JS, Stewart LC, et al. Acute intermittent hypoxia elicits sympathetic neuroplasticity independent of peripheral chemoreflex activation and spinal cord tissue hypoxia in a rodent model of high-thoracic spinal cord injury. Exp Neurol. 2025;384:115054. DOI: 10.1016/j.expneurol.2024.115054.
- Stožer A, Vodopivc P, Križančić BL. Pathophysiology of exercise-induced muscle damage and its structural, functional, metabolic, and clinical consequences. Physiol Res. 2020;69(4):565-98.
- Jüttner M, Ferreira-Cerca S. A Comparative Perspective on Ribosome Biogenesis: Unity and Diversity Across the Tree of Life. Methods Mol Biol. 2022;2533:22. DOI: 10.1007/978-1-0716-2501-9_1.
- Tymoshenko KR. Strukturno-funktsionalni perebudovy mikrohemodynamiky pry adaptatsii do fizychnoho navantazhennia [dysertatsiia]. K.: Instytut fiziolohiyi im. O.O. Bohomoltsya NAN Ukrayiny; 2020. 141 s. [in Ukrainian].
- Vital TM, Stein AM, de Melo Coelho FG, Arantes FJ, Teodorov E, Santos-Galduróz RF. Physical exercise and vascular endothelial growth factor (VEGF) in elderly: A systematic review. Arch Gerontol Geriatr. 2014;59(2):234-9. DOI: 10.1016/j.archger.2014.04.011.
Publication of the article:
«Bulletin of problems biology and medicine», 2025 Issue 3,178, 384-394 pages, index UDC 612.015.1:576.82