INFLUENCE OF SECRETORY FUNCTION OF SKELETAL MUSCLE ON REHABILITATION

Authors

  • H. M. Traverse
  • V. I. Horoshko
  • O. V. Hordiienko

DOI:

https://doi.org/10.32782/2522-1795.2023.14.12

Keywords:

irisin, skeletal muscles, myosins, myofibril fibers.

Abstract

It is a well-known fact that muscles secrete proteins called myokines and participate in many processes interacting with other tissues. Current studies have shown that exercise, stimulating the skeletal muscle system in vivo, leads to the release of myokines and causes a number of effects that explain the positive effect of exercise in the treatment of diseases of the musculoskeletal system. The purpose of the work was to summarize the latest scientific developments on the influence of physical activity on the secretory function of skeletal muscles and the relationship with other organs. To achieve the goal and solve certain tasks, the following research methods were used, in particular: problem-chronological; sociological; analytical; method of terminological analysis; method of scientific extrapolation; methods of multivariate statistical analysis and forecasting – for data processing. Research methods. As well as the methods of applied system analysis, elements of probability theory, failure software design methodology were used during the work. The development of methods for simplifying the structural and functional complexity of the model was used in the research process. Recent publications have focused much attention on one such myokine, namely the recently discovered protein irisin, which is secreted into the bloodstream from skeletal muscle during exercise from the membrane-bound precursor fibronectin type III. A series of studies on irisin has provided a new look at the mechanisms of exercise to improve bone density, counteract cartilage degeneration, and support the overall environmental homeostasis of the joint. These studies add to the understanding of the role of exercise in the fight against osteoarthritis and may provide significant assistance in the development of prevention and treatment of this common disease. Recent publications have focused on the protein irisin, which is secreted into the bloodstream from skeletal muscle during exercise from the membrane-bound precursor of type III fibronectin. Irisin promotes metabolic processes such as glucose homeostasis and adipose tissue replacement. It crosses the blood-brain barrier and initiates a neuroprotective genetic program in the hippocampus, which culminates in increased expression of brain-derived neurotrophic factor. Conclusion. Most studies report that irisin concentration is closely related to health status. Studies of exercise-induced muscle factor irisin will help to better understand and explain the beneficial effects of exercise in maintaining physical health, especially in the fight against aging and age-related degenerative changes.

References

Huh JY. The role of exercise-induced myokines in regulating metabolism. Arch Pharm Res. 2018 Jan;41(1):14-29. doi: 10.1007/ s12272-017-0994-y. Epub 2017 Nov 25. PMID: 29177585.

Jodeiri Farshbaf M, Alviña K. Multiple Roles in Neuroprotection for the Exercise Derived Myokine Irisin. Front Aging Neurosci. 2021 Apr 16;13: 649929. doi: 10.3389/ fnagi.2021.649929. PMID: 33935687; PMCID: PMC8086837.

Qi JY, Yang LK, Wang XS, Wang M, Li XB, Feng B, Wu YM, Liu SB, Zhang K. Mechanism of CNS regulation by irisin, a multifunctional protein. Brain Res Bull. 2022 Oct 1; 188:11–20. doi: 10.1016/j.brainresbull.2022.07.007. Epub 2022 Jul 15. PMID: 35850187.

Ning K, Wang Z, Zhang XA. Exercise-induced modulation of myokine irisin in bone and cartilage tissue-Positive effects on osteoarthritis: A narrative review. Front Aging Neurosci. 2022 Aug 19; 14:934406. doi: 10.3389/ fnagi.2022.934406. PMID: 36062149; PMCID: PMC9439853.

He Z, Li H, Han X, Zhou F, Du J, Yang Y, Xu Q, Zhang S, Zhang S, Zhao N, Yan M, Yu Z. Irisin inhibits osteocyte apoptosis by activating the Erk signaling pathway in vitro and attenuates ALCT-induced osteoarthritis in mice. Bone. 2020 Dec; 141:115573. doi: 10.1016/j.bone.2020.115573. Epub 2020 Aug 5.PMID: 32768686

Kirk B, Feehan J, Lombardi G, Duque G. Muscle, Bone, and Fat Crosstalk: the Biological Role of Myokines, Osteokines, and Adipokines. Curr Osteoporos Rep. 2020 Aug;18(4):388–400. doi: 10.1007/s11914-020-00599-y. PMID: 32529456.

Hain BA, Waning DL.Bone-Muscle Crosstalk: Musculoskeletal Complications of Chemotherapy. Curr Osteoporos Rep. 2022 Sep 10. doi: 10.1007/s11914-022-00749-4. Online ahead of print.PMID: 36087213 Review.

Hawker, G. A. (2019). Osteoarthritis is a serious disease. Clin. Exp. Rheumatol. 37(Suppl. 120), 3–6.

Ning K, Wang Z, Zhang XA. Exerciseinduced modulation of myokine irisin in bone and cartilage tissue-Positive effects on osteoarthritis: A narrative review. Front Aging Neurosci. 2022 Aug 19;14: 934406. doi: 10.3389/fnagi.2022. 934406. eCollection 2022.PMID: 36062149 Free PMC article. Review.

Bains, B. S. (2020). Sarcopenia and locomotive disorders in sedentary city lifestyle. Int. J. Aging Health Mov. 1, 8–12.

Bricca, A., Harris, L. K., Jager, M., Smith, S. M., Juhl, C. B., and Skou, S. T. (2020). Benefits and harms of exercise therapy in people with multimorbidity: a systematic review and meta-analysis of randomised controlled trials. Ageing Res. Rev. 63, 101166. doi: 10.1016/j. arr.2020.101166

Liu, L., Guo, J., Chen, X., Tong, X., Xu, J., and Zou, J. (2021). The role of irisin in Exercise-Mediated bone health. Front Cell Dev Biol. 9, 668759. doi: 10.3389/fcell.2021.668759

Tavassoli, H., Heidarianpour, A., and Hedayati, M. (2022). The effects of resistance exercise training followed by de-training on irisin and some metabolic parameters in type 2 diabetic rat model. Arch. Physiol. Biochem. 128, 240–247. doi: 10.1080/13813455.2019.1673432

Kubo, H., Asai, K., Kojima, K., Sugitani, A., Kyomoto, Y., and Okamoto, A., et al. (2019). Exercise ameliorates emphysema of cigarette Smoke-Induced COPD in mice through the Exercise-Irisin-Nrf2 axis. Int. J. Chron. Obstruct. Pulmon. Dis. 14, 2507–2516. doi: 10.2147/COPD.S226623

Cosio, P. L., Crespo-Posadas, M., Velarde-Sotres, A., and Pelaez, M. (2021). Effect of chronic resistance training on circulating irisin: systematic review and Meta-Analysis of randomized controlled trials. Int. J. Environ. Res. Public Health 18, 2476. doi: 10.3390/ ijerph18052476 16. Colpitts, B. H., Rioux, B. V., Eadie, A. L., Brunt, K. R., and Senechal, M. (2022). Irisin response to acute moderate intensity exercise and high intensity interval training in youth of different obesity statuses: a randomized crossover trial. Physiol. Rep. 10, e15198. doi: 10.14814/ phy2.15198

Jandova, T., Buendia-Romero, A., Polanska, H., Hola, V., Rihova, M., and Vetrovsky, T., et al. (2021). Long-Term effect of exercise on irisin blood Levels-Systematic review and Meta-Analysis. Healthcare. 9, 1438. doi: 10.3390/healthcare9111438

Mu, S., Ding, D., Ji, C., Wu, Q., Xia, Y., and Zhou, L., et al. (2020). Relationships between circulating irisin response to ice swimming and body composition in people with regular exercise experience. Front. Physiol. 11, 596896. doi: 10.3389/fphys.2020.596896

Sun, L. N., Li, X. L., Wang, F., Zhang, J., Wang, D. D., and Yuan, L., et al. (2017). High-intensity treadmill running impairs cognitive behavior and hippocampal synaptic plasticity of rats via activation of inflammatory response. J. Neurosci. Res. 95, 1611–1620. doi: 10.1002/jnr.23996

Belviranli, M., and Okudan, N. (2018). Exercise training increases cardiac, hepatic and circulating levels of brain-derived neurotrophic factor and irisin in young and aged rats. Horm. Mol. Biol. Clin. Investig. 36. doi: 10.1515/ hmbci-2018-0053

Babaei, P., and Azari, H. B. (2021). Exercise training improves memory performance in older adults: a narrative review of evidence and possible mechanisms. Front. Hum. Neurosci. 15, 771553. doi: 10.3389/fnhum.2021.771553

He, W., Wang, P., Chen, Q., and Li, C. (2020). Exercise enhances mitochondrial fission and mitophagy to improve myopathy following critical limb ischemia in elderly mice via the PGC1a/FNDC5/irisin pathway. Skelet. Muscle 10, 25. doi: 10.1186/s13395-020-00245-2

Bi, J., Yang, L., Wang, T., Zhang, J., Li, T., and Ren, Y., et al. (2020). Irisin improves autophagy of aged hepatocytes via increasing telomerase activity in liver injury. Oxid. Med. Cell. Longev. 2020, 6946037. doi: 10.1155/2020/6946037

Vadala, G., Di Giacomo, G., Ambrosio, L., Cannata, F., Cicione, C., and Papalia, R., et al. (2020). Irisin recovers osteoarthritic chondrocytes in vitro. Cells 9, 1478. doi: 10.3390/ cells9061478

Published

2023-04-19

How to Cite

Traverse Г. М., Horoshko В. І., & Hordiienko О. В. (2023). INFLUENCE OF SECRETORY FUNCTION OF SKELETAL MUSCLE ON REHABILITATION. Rehabilitation and Recreation, (14), 113–120. https://doi.org/10.32782/2522-1795.2023.14.12

Issue

Section

PHYSICAL THERAPY, OCCUPATIONAL THERAPY

Most read articles by the same author(s)

1 2 > >> 

Similar Articles

You may also start an advanced similarity search for this article.