The Effect of High-Intensity Interval Training (HIIT) on the Contents of Dynamin-Like Protein 1 (DRP1) and Optic Atrophy 1 (OPA1) in the Left Ventricle of Aged Male Rats

Document Type : Original Article (s)

Authors

1 Department of Physical Education and Sport Sciences, Aliabad Katoul Branch, Islamic Azad University, Aliabad Katoul, Iran

2 Department of Physical Education, Farhangian University, P.O. Box 14665-889, Tehran, Iran

Abstract

Background: Aging is accompanied by a gradual weakening of heart function, which can lead to an increase in the risk of cardiovascular diseases. HIIT, as a potent exercise intervention, seems to benefit heart function and mitochondrial health in elderly groups.
Methods: The present research is of an experimental type, conducted with 12 20-month-old Wistar male rats with an average weight of 400 ± 30 grams. The inclusion criteria were male rats aged 20 months and older, which were randomly divided into two HIIT and control groups (6 rats in each group). During the research, the control group had no activity, and the training group ran on the treadmill for eight weeks and five sessions weekly. The HIIT program was performed with high-intensity bouts of 85-95% of maximum speed (m/min) and active rest periods with an intensity of 40-55% of maximum speed (m/min) for each session per week. After 48 hours following the last training session, the rats were anesthetized, and the variables were measured using the western blot method. The data were analyzed through Shapiro-Wilk and independent t-test, and the significance level was considered P ≥ 0.05.
Findings: The results showed that eight weeks of HIIT caused a significant increase in DRP1 in the hearts of old rats, while it did not significantly change the content of OPA1 protein.
Conclusion: HIIT protocol seems to improve mitochondrial quality control in the heart of aged rats.

Highlights

Neda Aghaei Bahmanbeglou: Google Scholar, PubMed

Hamed Alizadeh Pahlavani: Google Scholar, PubMed

Habib Asgharpour: Google Scholar

Keywords

Main Subjects


  1. Steenman M, Lande G. Cardiac aging and heart disease in humans. Biophys Rev 2017; 9(2): 131-7.
  2. Stern S, Behar S, Gottlieb S. Aging and diseases of the heart. Circulation 2003; 108(14): e99-e101.
  3. Chaudhary KR, El-Sikhry H, Seubert JM. Mitochondria and the aging heart. J Geriatr Cardiol 2011; 8(3): 159-67.
  4. Dai D-F, Rabinovitch PS, Ungvari Z. Mitochondria and cardiovascular aging. Circ Res 2012; 110(8): 1109-24.
  5. Wu NN, Zhang Y, Ren J. Mitophagy, mitochondrial dynamics, and homeostasis in cardiovascular aging. Oxid Med Cell Longev 2019; 2019(1): 9825061.
  6. Chen L, Liu T, Tran A, Lu X, Tomilov AA, Davies V, et al. OPA 1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial Dysfunction and mtDNA Instability. J Am Heart Assoc 2012; 1(5): e003012.
  7. Poznyak AV, Kirichenko TV, Borisov EE, Shakhpazyan NK, Kartuesov AG, Orekhov AN. Mitochondrial implications in cardiovascular aging and diseases: the specific role of mitochondrial dynamics and shifts. Int J Mol Sci 2022; 23(6): 2951.
  8. Uchikado Y, Ikeda Y, Ohishi M. Current understanding of the pivotal role of mitochondrial dynamics in cardiovascular diseases and senescence. Front Cardiovasc Med 2022; 9: 905072.
  9. Chauhan A, Vera J, Wolkenhauer O. The systems biology of mitochondrial fission and fusion and implications for disease and aging. Biogerontology 2014; 15(1): 1-12.
  10. Liu YJ, McIntyre RL, Janssens GE, Houtkooper RH. Mitochondrial fission and fusion: A dynamic role in aging and potential target for age-related disease. Mech Ageing Dev 2020; 186: 111212.
  11. Ong S-B, Kalkhoran SB, Cabrera-Fuentes HA, Hausenloy DJ. Mitochondrial fusion and fission proteins as novel therapeutic targets for treating cardiovascular disease. Eur J Pharmacol 2015; 763(Pt A): 104–14.
  12. Wang C, Xing J, Zhao B, Wang Y, Zhang L, Wang Y, et al. The effects of high‐intensity interval training on exercise capacity and prognosis in heart failure and coronary artery disease: a systematic review and meta‐analysis. Cardiovasc Ther 2022; 2022: 4273809.
  13. Taylor JL, Barnes JN, Johnson BD. The utility of high intensity interval training to improve cognitive aging in heart disease patients. Int J Environ Res Public Health 2022; 19(24): 16926.
  14. Silva M, Baptista L, Neves R, França E, Loureiro H, Rezende M, et al. High intensity interval training improves health-related quality of life in adults and older adults with diagnosed cardiovascular risk. Journal of Physical Education and Sport 2019; 19(1): 611-8.
  15. Zafaranieh S, Choobineh S, Soori R. The effect of 12 weeks of aerobic exercise on mitochondrial dynamics in cardiac myocytes of type 2 diabetic rats. Sport Sciences for Health 2018; 14: 305-12.
  16. Lim AY, Chen Y-C, Hsu C-C, Fu T-C, Wang J-S. The effects of exercise training on mitochondrial function in cardiovascular diseases: A systematic review and meta-analysis. Int J Mol Sci 2022; 23(20): 12559.
  17. Zafaranieh S, Soori R. The effect of 12 weeks of high intensity interval training on mitochondrial dynamics in cardiac myocytes of type 2 diabetic rats [in Persian]. Journal of Sport Biosciences 2021; 13(1): 25-38.
  18. Garcia NF, Sponton AC, Delbin MA, Parente JM, Castro MM, Zanesco A, et al. Metabolic parameters and responsiveness of isolated iliac artery in LDLr-/-mice: role of aerobic exercise training. Am J Cardiovasc Dis 2017; 7(2): 64-71.
  19. Soori R, Gerami M, Pornemati P, Eskandari A. Effect of high intensity interval training and continus training on antioxidant enzymes in the heart of the old rats [in Persian]. J Gorgan Univ Med Sci 2019; 21(2): 26-31.
  20. Alizadeh R, Salehi O, Rezaeinezhad N, Hosseini SA. The effect of high intensity interval training with genistein supplementation on mitochondrial function in the heart tissue of elderly rats. Exp Gerontol 2023; 171: 112039.
  21. Sherafati-Moghadam M, Pahlavani HA, Daryanoosh F, Salesi M. The effect of high-intensity interval training (HIIT) on protein expression in Flexor Hallucis Longus (FHL) and soleus (SOL) in rats with type 2 diabetes. J Diabetes Metab Disord 2022; 21(2): 1499-508.
  22. Yan X, Shen Z, Yu D, Zhao C, Zou H, Ma B, et al. Nrf2 contributes to the benefits of exercise interventions on age-related skeletal muscle disorder via regulating Drp1 stability and mitochondrial fission. Free Radic Biol Med 2022; 178: 59-75.
  23. Kemi OJ, Wisløff U. High-intensity aerobic exercise training improves the heart in health and disease. J Cardiopulm Rehabil Prev 2010; 30(1): 2-11.
  24. Gu C, Yan J, Zhao L, Wu G, Wang Y-l. Regulation of mitochondrial dynamics by aerobic exercise in cardiovascular diseases. Front Cardiovasc Med 2022; 8: 788505.
  25. No M-H, Heo J-W, Yoo S-Z, Kim C-J, Park D-H, Kang J-H, et al. Effects of aging and exercise training on mitochondrial function and apoptosis in the rat heart. Pflugers Arch 2020; 472(2): 179-93.
  26. Wei X, Wu YE, Wang W, Zhang S, Liu D, Liu H. Decreased dynamin-related protein 1-related mitophagy induces myocardial apoptosis in the aging heart. Acta Biochim Biophys Sin (Shanghai) 2021; 53(10): 1354-66.
  27. Gusdon AM, Callio J, Distefano G, O'Doherty RM, Goodpaster BH, Coen PM, et al. Exercise increases mitochondrial complex I activity and DRP1 expression in the brains of aged mice. Exp Gerontol 2017; 90: 1-13.
  28. Moore TM, Zhou Z, Cohn W, Norheim F, Lin AJ, Kalajian N, et al. The impact of exercise on mitochondrial dynamics and the role of Drp1 in exercise performance and training adaptations in skeletal muscle. Mol Metab 2019; 21: 51-67.
  29. Robert P, Nguyen PMC, Richard A, Grenier C, Chevrollier A, Munier M, et al. Protective role of the mitochondrial fusion protein OPA1 in hypertension. FASEB J 2021; 35(7): e21678.
  30. Tezze C, Romanello V, Desbats MA, Fadini GP, Albiero M, Favaro G, et al. Age-associated loss of OPA1 in muscle impacts muscle mass, metabolic homeostasis, systemic inflammation, and epithelial senescence. Cell Metab 2017; 25(6): 1374-89.e6.
  31. Konopka AR, Suer MK, Wolff CA, Harber MP. Markers of human skeletal muscle mitochondrial biogenesis and quality control: effects of age and aerobic exercise training. J Gerontol A Biol Sci Med Sci 2014; 69(4): 371-8.
  32. Alizadeh Pahlavani H, Laher I, Knechtle B, Zouhal H. Exercise and mitochondrial mechanisms in patients with sarcopenia. Front Physiol 2022; 13: 1040381.
  33. Alizadeh Pahlavani H. Exercise therapy for people with sarcopenic obesity: myokines and adipokines as effective actors. Front Endocrinol (Lausanne) 2022; 13: 811751.