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Czasopismo

2020 | 79 | 2 |

Tytuł artykułu

Beneficial effects of voluntary over forced exercise on skeletal muscle structure and myokines’ expression

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Background: Myokines, a group of small proteins — mainly cytokines, are released by myocytes during muscular contraction and proved to have many biological effects locally or at systemic levels. The main objective was to study the morphological alterations and myokines expression in rat gastrocnemius muscle following forced compared to voluntary muscle contraction. Materials and methods: Thirty-six adult male Wistar rats were divided into three groups: control, voluntary exercise and forced swimming regimen. The experiment last for 3 weeks. The weight of rats and serum corticosterone levels were recorded. The gastrocnemius muscle samples were processed for histological and immunohistochemical study of different myokines. Results: The mean weight of rats showed no statistical difference between groups. Corticosterone level significantly increased after forced exercise. Voluntary exercise muscle fibres appeared hypertrophied with prominent transverse banding and dominating satellite cells. Forced exercise muscle showed atrophied widely spaced muscle fibres and inflammatory cell infiltrate. Voluntary exercise significantly increased optic density of interleukin 6, macrophage inhibitory and brain derived neurotrophic factors, whereas the forced exercise group showed significant decrease in their optic densities. The optic density of vascular endothelial growth factor significantly decreased in the forced exercise group. Forced exercise could be harmful to the skeletal muscle fibres and it decreases the secretion of important myokines. Further, forced exercise significantly increases the serum corticosterone level. Conclusions: The use of exercise for the attainment of healthy life style or in psycho- or neuro-therapy should follow a thoroughly studied programme for welfare of human health. (Folia Morphol 2020; 79, 2: 350–358)

Słowa kluczowe

Wydawca

-

Czasopismo

Rocznik

Tom

79

Numer

2

Opis fizyczny

p.350-358,fig.,ref.

Twórcy

  • Department of Anatomy, Faculty of Medicine, Taibah University, Saudi Arabia
  • Department of Anatomy, Faculty of Medicine, Tanta University, Egypt
autor
  • Department of Anatomy, Faculty of Dentistry, Modern Sciences and Arts University, Egypt
autor
  • Department of Anatomy, Faculty of Medicine, King Abdulaziz University, Saudi Arabia
  • Yousef Abdullatif Jameel Chair of Prophetic Medical Applications, Saudi Arabia
autor
  • Department of Anatomy, College of Medicine, Taibah University, Almadinah Almunawwarah, Saudi Arabia
autor
  • Orthopedic Surgery, Ministry of Interior Hospitals, Cairo, Egypt

Bibliografia

  • 1. Adlard PA, Perreau VM, Pop V, et al. Voluntary exercise decreases amyloid load in a transgenic model of Alzheimer’s disease. J Neurosci. 2005; 25(17): 4217–4221, doi: 10.1523/JNEUROSCI.0496-05.2005, indexed in Pubmed: 15858047.
  • 2. Armstrong RB, Ogilvie RW, Schwane JA. Eccentric exercise-induced injury to rat skeletal muscle. J Appl Physiol Respir Environ Exerc Physiol. 1983; 54(1): 80–93, doi: 10.1152/jappl.1983.54.1.80, indexed in Pubmed: 6826426.
  • 3. Arnold JC, Salvatore MF. Getting to compliance in forced exercise in rodents: a critical standard to evaluate exercise impact in aging-related disorders and disease. J Vis Exp. 2014(90), doi: 10.3791/51827, indexed in Pubmed: 25178094.
  • 4. Ayuob NN, Ali SS, Suliaman M, et al. The antidepressant effect of musk in an animal model of depression: a histopathological study. Cell Tissue Res. 2016; 366(2): 271–284, doi: 10.1007/s00441-016-2468-9, indexed in Pubmed: 27481508.
  • 5. Bazgir B, Fathi R, Rezazadeh Valojerdi M, et al. Satellite cells contribution to exercise mediated muscle hypertrophy and repair. Cell J. 2017; 18(4): 473–484, doi: 10.22074/cellj.2016.4714, indexed in Pubmed: 28042532.
  • 6. Bellamy LM. Temporal Pattern of Type Ii Fibre- Specific Satellite Cell Expansion To Exercise Correlates With Human Muscle Hypertrophy: Potential Role for Myostatin. 2012.
  • 7. Clow C, Jasmin BJ. Brain-derived neurotrophic factor regulates satellite cell differentiation and skeltal muscle regeneration. Mol Biol Cell. 2010; 21(13): 2182–2190, doi: 10.1091/mbc.e10-02-0154, indexed in Pubmed: 20427568.
  • 8. Contarteze RV, Manchado FD, Gobatto CA, et al. Stress biomarkers in rats submitted to swimming and treadmill running exercises. Comp Biochem Physiol A Mol Integr Physiol. 2008; 151(3): 415–422, doi: 10.1016/j.cbpa.2007.03.005, indexed in Pubmed: 17428717.
  • 9. Eldomiaty MA, Almasry SM, Desouky MK, et al. Voluntary running improves depressive behaviours and the structure of the hippocampus in rats: A possible impact of myokines. Brain Res. 2017; 1657: 29–42, doi: 10.1016/j.brainres.2016.12.001, indexed in Pubmed: 27919728.
  • 10. Gavin TP, Westerkamp LM, Zwetsloot KA. Soleus, plantaris and gastrocnemius VEGF mRNA responses to hypoxia and exercise are preserved in aged compared with young female C57BL/6 mice. Acta Physiol (Oxf). 2006; 188(2): 113–121, doi: 10.1111/j.1748-1716.2006.01609.x, indexed in Pubmed: 16948798.
  • 11. Gleeson M. Immune function in sport and exercise. J Appl Physiol (1985). 2007; 103(2): 693–699, doi: 10.1152/japplphysiol.00008.2007, indexed in Pubmed: 17303714.
  • 12. Grizzle WE. Special symposium: fixation and tissue processing models. Biotech Histochem. 2009; 84(5): 185–193, doi: 10.3109/10520290903039052, indexed in Pubmed: 19886755.
  • 13. Johnson SE, Allen RE. Proliferating cell nuclear antigen (PCNA) is expressed in activated rat skeletal muscle satellite cells. J Cell Physiol. 1993; 154(1): 39–43, doi: 10.1002/jcp.1041540106, indexed in Pubmed: 8093452.
  • 14. Jonsson J. Effect of voluntary exercise on BDNF/TrkB gene expression and alcohol intake Josefine Jonsson. Master Thesis. 2012.
  • 15. Klein GL. The effect of glucocorticoids on bone and muscle. Osteoporos Sarcopenia. 2015; 1(1): 39–45, doi: 10.1016/j.afos.2015.07.008, indexed in Pubmed: 26557727.
  • 16. Muñoz-Cánoves P, Scheele C, Pedersen BK, et al. Interleukin-6 myokine signaling in skeletal muscle: a double-edged sword? FEBS J. 2013; 280(17): 4131–4148, doi: 10.1111/febs.12338, indexed in Pubmed: 23663276.
  • 17. Pedersen BK, Steensberg A, Fischer C, et al. Searching for the exercise factor: is IL-6 a candidate? J Muscle Res Cell Motil. 2003; 24(2-3): 113–119, doi: 10.1023/a:1026070911202, indexed in Pubmed: 14609022.
  • 18. Perdiguero E, Ruiz-Bonilla V, Gresh L, et al. Genetic analysis of p38 MAP kinases in myogenesis: fundamental role of p38alpha in abrogating myoblast proliferation. EMBO J. 2007; 26(5): 1245–1256, doi: 10.1038/sj.emboj.7601587, indexed in Pubmed: 17304211.
  • 19. Porsolt RD. Animal models of depression: utility for transgenic research. Rev Neurosci. 2000; 11(1): 53–58, doi: 10.1515/revneuro.2000.11.1.53, indexed in Pubmed: 10716655.
  • 20. Rodriguez I, Diaz A, Vaamonde D. Assessment of the effect of prolonged forced swimming on CD-1 mice sperm morphology with and without antioxidant supplementation. Andrologia. 2016; 48(3): 277–281, doi: 10.1111/and.12443, indexed in Pubmed: 26032180.
  • 21. Rowe GC, Safdar A, Arany Z. Running forward: new frontiers in endurance exercise biology. Circulation. 2014; 129(7): 798–810, doi: 10.1161/CIRCULATIONAHA.113.001590, indexed in Pubmed: 24550551.
  • 22. Schnyder S, Handschin C. Skeletal muscle as an endocrine organ: PGC-1a, myokines and exercise. Bone. 2015; 80: 115–125, doi: 10.1016/j.bone.2015.02.008, indexed in Pubmed: 26453501.
  • 23. So B, Kim HJ, Kim J, et al. Exercise-induced myokines in health and metabolic diseases. Integr Med Res. 2014; 3(4): 172–179, doi: 10.1016/j.imr.2014.09.007, indexed in Pubmed: 28664094.
  • 24. Tang K, Breen EC, Gerber HP, et al. Capillary regression in vascular endothelial growth factor-deficient skeletal muscle. Physiol Genomics. 2004; 18(1): 63–69, doi: 10.1152/physiolgenomics.00023.2004, indexed in Pubmed: 15084712.
  • 25. Tang K, Breen EC, Wagner H, et al. HIF and VEGF relationships in response to hypoxia and sciatic nerve stimulation in rat gastrocnemius. Respir Physiol Neurobiol. 2004; 144(1): 71–80, doi: 10.1016/j.resp.2004.04.009, indexed in Pubmed: 15522704.
  • 26. Varghese F, Bukhari AB, Malhotra R, et al. IHC Profiler: an open source plugin for the quantitative evaluation and automated scoring of immunohistochemistry images of human tissue samples. PLoS One. 2014; 9(5): e96801, doi: 10.1371/journal.pone.0096801, indexed in Pubmed: 24802416.
  • 27. Webster I, Du Toit EF, Huisamen B. Peer reviewed Peer reviewed short communication the effect of long term swim training on physiological stress levels in the rat. Med Tech. 2010; 24(2): 37–40.
  • 28. Wen F, Zheng J, Yu J, et al. Macrophage migration inhibitory factor in the regulation of myoblast proliferation and differentiation. Biosci Biotechnol Biochem. 2016; 80(7): 1313–1320, doi: 10.1080/09168451.2016.1153951, indexed in Pubmed: 26927414.
  • 29. Wisse BE, Schwartz MW. The skinny on neurotrophins. Nat Neurosci. 2003; 6(7): 655–656, doi: 10.1038/nn0703-655, indexed in Pubmed: 12830151.

Typ dokumentu

Bibliografia

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