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Comparative effects of high-intensity interval training and moderate-intensity continuous training on soleus muscle fibronectin type III domain-containing protein 5, myonectin and glucose transporter type 4 gene expressions: a study on the diabetic rat model

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Abstract

Background

The increase in fibronectin type-III domain-containing protein 5 (FNDC5), myonectin, and glucose transporter 4 (GLUT4) leads to a decrease in diabetes; meanwhile, exercise training can affect these factors. The result regarding the comparison between the effect of high-intensity interval training (HIIT) and that of moderate-intensity continuous training (MICT) is confusing. Thus, the present study investigated the comparative effects of HIIT and MICT on soleus muscle FNDC5, myonectin, and GLUT4 gene expressions in the diabetic rat model.

Methods and results

Seventy-two male Wistar rats (weight 200 g ± 20) were randomly and equally assigned to six groups: control-healthy, MICT-healthy, HIIT-healthy, control-diabetes, MICT-diabetes, and HIIT-diabetes. At the first level, Streptozotocin (STZ) was utilized to induce diabetes in rats (at a dose of 55 mg/kg). After that, the training groups performed HIIT and MICT programs on the rodent treadmill for 6 weeks (five-session/week). Twenty-four hours after the last intervention, soleus muscle was removed, and sent to a research facility for future examinations. HIIT and MICT increased the muscle FNDC5, myonectin, and GLUT4 gene expression compared to the control group (P < 0.05). The type of training had no significant effect on the FNDC5 (P > 0.05), while the MICT program induced a greater increase in the myonec ztin and GLUT4 compared to the HIIT program (P < 0.05). Meanwhile, a positive relationship between all variables was observed.

Conclusions

Exercise training has a beneficial effect on diabetes conditions via the effect of FNDC5, myonectin, and GLUT4. Due to the correlation between myonectin and GLUT4 shown in the present study, physical activity may alter myonectin through its effect on GLUT requiring further investigation by subsequent studies.

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Data availability

All raw data used to analyze these results are freely available on reasonable request.

References

  1. Glovaci D, Fan W, Wong ND (2019) Epidemiology of diabetes mellitus and cardiovascular disease. Curr Cardiol Rep 21(4):1–8

    Article  Google Scholar 

  2. Shoaib A et al (2020) Increased serum lipid profile and development of vascular complications in diabetic individuals—a comparative study. PJMHS 14(4):1–2

  3. Dimitriadis GD et al (2021) Regulation of postabsorptive and postprandial glucose metabolism by insulin-dependent and insulin-independent mechanisms: an integrative approach. Nutrients 13(1):159

    Article  CAS  PubMed Central  Google Scholar 

  4. Stanford KI, Goodyear LJ (2014) Exercise and type 2 diabetes: molecular mechanisms regulating glucose uptake in skeletal muscle. Adv Physiol Educ 38(4):308–314

    Article  PubMed  PubMed Central  Google Scholar 

  5. Rodríguez A et al (2017) Crosstalk between adipokines and myokines in fat browning. Acta Physiol 219(2):362–381

    Article  Google Scholar 

  6. Gamas L, Matafome P, Seiça R (2015) Irisin and myonectin regulation in the insulin resistant muscle: implications to adipose tissue: muscle crosstalk. J Diabetes Res 2015:359159–359159

    Article  PubMed  PubMed Central  Google Scholar 

  7. Arhire LI, Mihalache L, Covasa M (2019) Irisin: a hope in understanding and managing obesity and metabolic syndrome. Front Endocrinol. https://doi.org/10.3389/fendo.2019.00524

    Article  Google Scholar 

  8. Chen N et al (2016) Irisin, an exercise-induced myokine as a metabolic regulator: an updated narrative review. Diabetes Metab Res Rev 32(1):51–59

    Article  CAS  PubMed  Google Scholar 

  9. Perakakis N et al (2017) Physiology and role of irisin in glucose homeostasis. Nat Rev Endocrinol 13(6):324–337

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Gizaw M, Anandakumar P, Debela T (2017) A review on the role of irisin in insulin resistance and type 2 diabetes mellitus. J Pharmacopuncture 20(4):235–242

    PubMed  PubMed Central  Google Scholar 

  11. Xin C et al (2016) Irisin improves fatty acid oxidation and glucose utilization in type 2 diabetes by regulating the AMPK signaling pathway. Int J Obes (Lond) 40(3):443–451

    Article  CAS  Google Scholar 

  12. Seldin MM et al (2012) Myonectin (CTRP15), a novel myokine that links skeletal muscle to systemic lipid homeostasis. J Biol Chem 287(15):11968–11980

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Gamas L, Matafome P, Seiça R (2015) Irisin and myonectin regulation in the insulin resistant muscle: implications to adipose tissue: muscle crosstalk. J Diabetes Res. https://doi.org/10.1155/2015/359159

    Article  PubMed  PubMed Central  Google Scholar 

  14. Tayebi SM et al (2019) Plasma retinol-binding protein-4 and tumor necrosis factor-α are reduced in postmenopausal women after combination of different intensities of circuit resistance training and Zataria supplementation. Sport Sci Health 15(3):551–558

    Article  PubMed  PubMed Central  Google Scholar 

  15. Brandt C, Pedersen BK (2010) The role of exercise-induced myokines in muscle homeostasis and the defense against chronic diseases. J Biomed Biotechnol. https://doi.org/10.1155/2010/520258

    Article  PubMed  PubMed Central  Google Scholar 

  16. Mathur N, Pedersen BK (2008) Exercise as a mean to control low-grade systemic inflammation. Mediators Inflamm. https://doi.org/10.1155/2008/109502

    Article  PubMed  Google Scholar 

  17. Arabzadeh E et al (2020) Alteration of follistatin-like 1, neuron-derived neurotrophic factor, and vascular endothelial growth factor in diabetic cardiac muscle after moderate-intensity aerobic exercise with insulin. Sport Sci Health. https://doi.org/10.1007/s11332-020-00631-9

    Article  Google Scholar 

  18. Fisher G et al (2015) High Intensity interval- vs moderate intensity-training for improving cardiometabolic health in overweight or obese males: a randomized controlled trial. PLoS One. https://doi.org/10.1371/journal.pone.0138853

    Article  PubMed  PubMed Central  Google Scholar 

  19. Stein RA et al (1990) Effects of different exercise training intensities on lipoprotein cholesterol fractions in healthy middle-aged men. Am Heart J 119(2 Pt 1):277–283

    Article  CAS  PubMed  Google Scholar 

  20. O’Donovan G et al (2005) Changes in cardiorespiratory fitness and coronary heart disease risk factors following 24 wk of moderate- or high-intensity exercise of equal energy cost. J Appl Physiol. https://doi.org/10.1152/japplphysiol.01310.2004

    Article  PubMed  Google Scholar 

  21. Rahmati-Ahmadabad S et al (2019) High-intensity interval training has a greater effect on reverse cholesterol transport elements compared with moderate-intensity continuous training in obese male rats. Eur J Prev Cardiol. https://doi.org/10.1177/2047487319887828

    Article  PubMed  Google Scholar 

  22. Tine Kartinah N et al (2018) The effects of exercise regimens on irisin levels in obese rats model: comparing high-intensity intermittent with continuous moderate-intensity training. Biomed Res Int 2018:4708287

    Article  PubMed  PubMed Central  Google Scholar 

  23. Teimourian M, Fatolahi H, Mateenhomaei H (2020) Effect of different exercise mode and ursolic acid supplementation on FNDC5 and UCP1 gene expression and plasma irisin in rats. Int J Sports Exerc Med. https://doi.org/10.23937/2469-5718/1510160

    Article  Google Scholar 

  24. Chavanelle V et al (2017) Effects of high-intensity interval training and moderate-intensity continuous training on glycaemic control and skeletal muscle mitochondrial function in db/db mice. Sci Rep 7(1):204

    Article  PubMed  PubMed Central  Google Scholar 

  25. Arabzadeh E, Mirdar S, Fathi Z (2015) Measurement of levels of lung HIF-1α protein in response to tapering for 14-and 21-day with nigella sativa supplementation in maturing rat, with histological study. Sport Sciences for Health 11(2):195–202

    Article  Google Scholar 

  26. Arabzadeh E, Mirdar S, Moradiani H (2016) Nigella sativa supplementation attenuates exercise-induced bronchoconstriction in the maturing rat: a histometric and histologic study. Comp Clin Pathol 25(1):1–5

    Article  CAS  Google Scholar 

  27. Yoon H et al (2015) Moderate exercise training attenuates inflammatory mediators in DRG of Type 1 diabetic rats. Exp Neurol 267:107–114

    Article  CAS  PubMed  Google Scholar 

  28. Grant CW et al (2012) Development of standardized insulin treatment protocols for spontaneous rodent models of type 1 diabetes. Comp Med 62(5):381–390

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Bedford TG et al (1979) Maximum oxygen consumption of rats and its changes with various experimental procedures. J Appl Physiol 47(6):1278–1283

    Article  CAS  PubMed  Google Scholar 

  30. Leandro CG et al (2007) A program of moderate physical training for Wistar rats based on maximal oxygen consumption. J Strength Cond Res 21(3):751

    PubMed  Google Scholar 

  31. Lade CG et al (2018) Effects of moderate intensity endurance training vs high intensity interval training on weight gain, cardiorespiratory capacity, and metabolic profile in postnatal overfed rats. Diabetol Metab Syndrome. https://doi.org/10.1186/s13098-018-0374-x

    Article  Google Scholar 

  32. Kurdiova T et al (2014) Exercise-mimicking treatment fails to increase Fndc5 mRNA & irisin secretion in primary human myotubes. Peptides 56:1–7

    Article  CAS  PubMed  Google Scholar 

  33. Timmons JA et al. (2012) Is irisin a human exercise gene? Nature 488(7413):E9–10; discussion E10–1

  34. Park KH et al (2013) Circulating irisin in relation to insulin resistance and the metabolic syndrome. J Clin Endocrinol Metab 98(12):4899–4907

    Article  CAS  PubMed  Google Scholar 

  35. Li K et al (2017) Myonectin predicts the development of type 2 diabetes. J Clin Endocrinol Metab 103(1):139–147

    Article  Google Scholar 

  36. Bostrom P et al (2012) A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature 481(7382):463–468

    Article  PubMed  PubMed Central  Google Scholar 

  37. Erickson HP (2013) Irisin and FNDC5 in retrospect: an exercise hormone or a transmembrane receptor? Adipocyte 2(4):289–293

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Gouni-Berthold I et al (2013) Effects of lipid-lowering drugs on irisin in human subjects in vivo and in human skeletal muscle cells ex vivo. PLoS ONE. https://doi.org/10.1371/journal.pone.0072858

    Article  PubMed  PubMed Central  Google Scholar 

  39. Huh JY et al (2014) Exercise-induced irisin secretion is independent of age or fitness level and increased irisin may directly modulate muscle metabolism through AMPK activation. J Clin Endocrinol Metab 99(11):E2154–E2161

    Article  CAS  PubMed  Google Scholar 

  40. Lee HJ et al (2015) Irisin, a novel myokine, regulates glucose uptake in skeletal muscle cells via AMPK. Mol Endocrinol 29(6):873–881

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Yang Z et al (2015) Decreased irisin secretion contributes to muscle insulin resistance in high-fat diet mice. Int J Clin Exp Pathol 8(6):6490–6497

    PubMed  PubMed Central  Google Scholar 

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Authors and Affiliations

Authors

Contributions

HSH conceived the study. SRA and FR carried out the experiments. GHM and SRA provided methodological advice and materials. HSH and FR wrote the manuscript. All authors agreed upon the final manuscript.

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Correspondence to Hossein Shirvani.

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The authors declare that they have no conflict of interest.

Ethical approval

This study was conducted following the National Institutes of Health (NIH) guidelines. Moreover, this study was performed with the written permission of the research deputy of Baqiyatallah University and has an ethical code (IR.BMSU.REC.1396.649).

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Animal study.

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Rahmati-Ahmadabad, S., Rostamkhani, F., Meftahi, G.H. et al. Comparative effects of high-intensity interval training and moderate-intensity continuous training on soleus muscle fibronectin type III domain-containing protein 5, myonectin and glucose transporter type 4 gene expressions: a study on the diabetic rat model. Mol Biol Rep 48, 6123–6129 (2021). https://doi.org/10.1007/s11033-021-06633-1

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