ISSN 2415-3060 (print), ISSN 2522-4972 (online)
  • 6 of 45
Up
УЖМБС 2023, 8(1): 50–55
https://doi.org/10.26693/jmbs08.01.050
Medicine. Reviews

The Effect of Physical Activity on the Secretory Function of Muscles and Bone Tissue in Humans

Traverse Galina 1, Horoshko Viktoriia 1, Danylchenko Svitlana 2
Abstract

The purpose of the study was to summarize new literature data on the effect of physical activity on the secretory function of skeletal muscles and their relationship with organs. Materials and methods. Analytical methods were used in the study. The search for scientific information was carried out in databases of search systems. Results. Muscles secrete proteins called myokines, which are involved in a variety of processes by interacting with tissues. Current research has shown that exercise, by stimulating the skeletal muscle system in vivo, leads to the release of myokines and causes several effects that explain the positive effect of exercise in the treatment of several diseases of the musculoskeletal system. Skeletal muscles synthesize and secrete a wide range of myokines that contribute to various functions in organs, including the brain. Recent publications have focused much attention on one such myokine, the recently discovered protein irisin, which is secreted into the bloodstream from skeletal muscle during exercise from the membrane-bound precursor fibronectin type III. Irisin promotes metabolic processes such as glucose homeostasis and the darkening of white adipose tissue. Irisin also crosses the blood-brain barrier and initiates a neuroprotective genetic program in the hippocampus, which culminates in increased expression of brain-derived neurotrophic factors. Most studies report that irisin concentration is closely related to health status. For example, irisin levels are significantly lower in patients with obesity, osteoporosis/fracture, muscular atrophy, Alzheimer's disease, and cardiovascular disease. Over the past decade, several myokines have been discovered, expanding our understanding of how muscles interact with other organs. In recent publications, a lot of attention is paid to the recently discovered protein irisin, which contributes to metabolic processes. A series of studies on irisin have provided new insights into the mechanisms of exercise to improve bone density, counteract cartilage degeneration, and maintain overall joint environmental homeostasis. These studies further contribute to the understanding of the role of exercise in the fight against osteoarthritis and may provide important assistance in advancing the prevention and treatment of this common disease. Research on the exercise-induced muscle factor irisin will help to better understand and explain the beneficial effects of exercise on maintaining physical health, especially in the fight against aging and age-related degenerative changes. Conclusion. Thus, exercise-induced stimulation of bioactive cytokines increases muscle anabolism, bone formation, mitochondrial biogenesis, glucose utilization, and fatty acid oxidation, and reduces chronic inflammation

Keywords: skeletal muscles, myokines, protein irisin, bone density, environmental homeostasis, age-related degenerative changes

Full text: PDF (Ua) 247K

References
  1. Babaei P, Azari HB. Exercise training improves memory performance in older adults: a narrative review of evidence and possible mechanisms. Front Hum Neurosci. 2021;15:771553. PMID: 35153701. PMCID: PMC8829997. https://doi.org/10.3389/fnhum.2021.771553
  2. Bains BS. Sarcopenia and locomotive disorders in the sedentary city lifestyle. Int J Aging Health Mov. 2020;1:8-12.
  3. Belviranlı M, Okudan N. 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. 2018 Oct 26;36(3). PMID: 30367793. https://doi.org/10.1515/hmbci-2018-0053
  4. Bi J, Yang L, Wang T, Zhang J, Li T, Ren Y, et al. Irisin improves the autophagy of aged hepatocytes via increasing telomerase activity in liver injury. Oxid Med Cell Longev. 2020 Jan 2;2020:6946037. PMID: 31976032. PMCID: PMC6959141. https://doi.org/10.1155/2020/6946037
  5. Bricca A, Harris LK, Jäger M, Smith SM, Juhl CB, Skou ST. Benefits and harms of exercise therapy in people with multimorbidity: a systematic review and meta-analysis of randomised controlled trials. Ageing Res Rev. 2020 Nov;63:101166. PMID: 32896665. PMCID: PMC7116122. https://doi.org/10.1016/j.arr.2020.101166
  6. Colpitts BH, Rioux BV, Eadie AL, Brunt KR, Sénéchal M. Irisin response to acute moderate intensity exercise and high intensity interval training in youth of different obesity statuses: a randomized crossover trial. Physiol Rep. 2022 Feb;10(4):e15198. PMID: 35224871. PMCID: PMC8883234. https://doi.org/10.14814/phy2.15198
  7. Cosio PL, Crespo-Posadas M, Velarde-Sotres Á, Pelaez M. Effect of chronic resistance training on circulating irisin: systematic review and Meta-Analysis of randomized controlled trials. Int J Environ Res Public Health. 2021 Mar 3;18(5):2476. PMID: 33802329. PMCID: PMC7967601. https://doi.org/10.3390/ijerph18052476
  8. Hain BA, Waning DL. Bone-Muscle Crosstalk: Musculoskeletal Complications of Chemotherapy. Curr Osteoporos Rep. 2022 Dec;20(6):433-441. PMID: 36087213. https://doi.org/10.1007/s11914-022-00749-4
  9. Hawker GA. Osteoarthritis is a serious disease. Clin Exp Rheumatol. 2019;37(Suppl 120):3-6.
  10. He Z, Li H, Han X, Zhou F, Du J, Yang Y, et al. Irisin inhibits osteocyte apoptosis by activating the Erk signaling pathway in vitro and attenuates ALCT-induced osteoarthritis in mice. Bone. 2020 Dec;141:115573. PMID: 32768686. https://doi.org/10.1016/j.bone.2020.115573
  11. He W, Wang P, Chen Q, Li C. Exercise enhances mitochondrial fission and mitophagy to improve myopathy following critical limb ischemia in elderly mice via the PGC1a/FNDC5/irisin pathway. Skelet Muscle. 2020 Sep 15;10(1):25. PMID: 32933582. PMCID: PMC7490877. https://doi.org/10.1186/s13395-020-00245-2
  12. Huh JY. The role of exercise-induced myokines in regulating metabolism. Arch Pharm Res. 2018 Jan;41(1):14-29. PMID: 29177585.
  13. https://doi.org/10.1007/s12272-017-0994-y
  14. Jandova T, Buendia-Romero A, Polanska H, Hola V, Rihova M, Vetrovsky T, et al. Long-Term effect of exercise on irisin blood Levels-Systematic review and Meta-Analysis. Healthcare (Basel). 2021 Oct 25;9(11):1438. PMID: 34828485ю PMCID: PMC8618299. https://doi.org/10.3390/healthcare9111438
  15. Jodeiri Farshbaf M, Alviña K. Multiple Roles in Neuroprotection for the Exercise Derived Myokine Irisin. Front Aging Neurosci. 2021 Apr 16;13:649929. https://doi.org/10.3389/fnagi.2021.649929. PMID: 33935687. PMCID: PMC8086837. https://doi.org/10.3389/fnagi.2021.649929
  16. 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. PMID: 32529456.
  17. https://doi.org/10.1007/s11914-020-00599-y
  18. Kubo H, Asai K, Kojima K, Sugitani A, Kyomoto Y, Okamoto A, et al. Exercise ameliorates emphysema of cigarette Smoke-Induced COPD in mice through the Exercise-Irisin-Nrf2 axis. Int J Chron Obstruct Pulmon Dis. 2019 Nov 14;14:2507-2516. PMID: 31814716. PMCID: PMC6862806. https://doi.org/10.2147/COPD.S226623
  19. Liu L, Guo J, Chen X, Tong X, Xu J, Zou J. The role of irisin in Exercise-Mediated bone health. Front Cell Dev Biol. 2021;9:668759. PMID: 34017836. PMCID: PMC8129548. https://doi.org/10.3389/fcell.2021.668759
  20. Mu S, Ding D, Ji C, Wu Q, Xia Y, Zhou L, et al. Relationships between circulating irisin response to ice swimming and body composition in people with regular exercise experience. Front Physiol. 2021 Jan 13;11:596896. PMID: 33519505. PMCID: PMC7838676. https://doi.org/10.3389/fphys.2020.596896
  21. 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. PMID: 36062149. PMCID: PMC9439853. https://doi.org/10.3389/fnagi.2022.934406
  22. Qi JY, Yang LK, Wang XS, Wang M, Li XB, Feng B, et al. Mechanism of CNS regulation by irisin, a multifunctional protein. Brain Res Bull. 2022 Oct 1;188:11-20. PMID: 35850187. https://doi.org/10.1016/j.brainresbull.2022.07.007
  23. Sun LN, Li XL, Wang F, Zhang J, Wang DD, Yuan L, et al. High-intensity treadmill running impairs cognitive behavior and hippocampal synaptic plasticity of rats via activation of inflammatory response. J Neurosci Res. 2017;95:1611-1620. PMID: 27918079. https://doi.org/10.1002/jnr.23996
  24. Tavassoli H, Heidarianpour A, Hedayati M. 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. 2022;128:240-247. PMID: 31588806. https://doi.org/10.1080/13813455.2019.1673432
  25. Vadala G, Di Giacomo G, Ambrosio L, Cannata F, Cicione C, Papalia R, et al. Irisin recovers osteoarthritic chondrocytes in vitro. Cells. 2020 Jun 17;9(6):1478. PMID: 32560375. PMCID: PMC7348865. https://doi.org/10.3390/cells9061478