The Attenuating Effect of High-Intensity Interval Training and Nicotinamide Mononucleotide Supplementation on Aging-Related Oxidative Stress in Rat's Heart Tissue

Document Type : Original Articles

Authors

1 PhD Student in Exercise Physiology, Department of Exercise Physiology, South Tehran Branch, Islamic Azad University, Tehran, Iran

2 Assistant Professor of Exercise Physiology, Department of Exercise Physiology, South Tehran Branch, Islamic Azad University, Tehran, Iran

3 Associate Professor, Department of Exercise Physiology, South Tehran Branch, Islamic Azad University, Tehran, Iran

4 Assistant Professor of exercise Physiology, Department of exercise Physiology, Parand Branch, Islamic Azad University, Tehran, Iran

10.22122/jrrs.v16i0.3634

Abstract

Introduction: Numerous studies have shown attenuating effects of nicotinamide mononucleotide (NMN) and high-intensity interval exercise (HIIT) training on reducing oxidative stress. Therefore, in the present study, we evaluated the effect of HIIT and NMN supplementation on the oxidative stress markers in cardiac tissue of rats.Materials and Methods: 48 sprago dauli rats with an average age of 8 to 10 months were randomly divided into 6 groups of pretest control, control, sham (normal saline), HIIT, NMN supplementation, and combination (HIIT + NMN). The HIIT and combination groups performed HIIT on the treadmill for 8 weeks, 3 sessions per week. NMN with a dose of 500 mg per kilogram body weight was administered intra-peritoneally in the NMN and combination groups. 24 hours after the last training and NMN administration, the animals were sacrificed, and their hearts were removed for evaluating oxidative stress factors [malondialdehyde (MDA), protein carbonyl (PC), superoxide dismutase (SOD), and glutathione peroxidase (GPx)]. One-way ANOVA test was used for statistical analysis.Results: The expression of GPx gene in the groups receiving NMN, HIIT, and combination was significantly higher compared to the pretest control, control, and sham groups (P < 0.050). Moreover, the levels of MDA and PC were lower in NMN, HIIT, and combination groups compared to the pre-test control, control, and sham (P < 0.050). The highest reduction was seen in the combination group (P < 0.001).Conclusion: It seems that regular consumption of NMN and/or HIIT may attenuate oxidative stress in the cardiac tissue; however, combinations of NMN and HIIT significantly improves the effects of sole interventions.

Keywords

  1. Harman D. The free radical theory of aging. Antioxid Redox Signal 2003; 5(5): 557-61.
  2. Salisbury D, Bronas U. Reactive oxygen and nitrogen species: Impact on endothelial dysfunction. Nurs Res 2015; 64(1): 53-66.
  3. Kalantari H, Foruozandeh H, Khodayar MJ, Siahpoosh A, Saki N, Kheradmand P. Antioxidant and hepatoprotective effects of Capparis spinosa L. fractions and Quercetin on tert-butyl hydroperoxide- induced acute liver damage in mice. J Tradit Complement Med 2018; 8(1): 120-7.
  4. Liguori I, Russo G, Curcio F, Bulli G, Aran L, Della-Morte D, et al. Oxidative stress, aging, and diseases. Clin Interv Aging 2018; 13: 757-72.
  5. Sergiev PV, Dontsova OA, Berezkin GV. Theories of aging: an ever-evolving field. Acta Naturae 2015; 7(1): 9-18.
  6. Aronow WS. Heart disease and aging. Med Clin North Am 2006; 90(5): 849-62.
  7. Bogdanis GC, Stavrinou P, Fatouros IG, Philippou A, Chatzinikolaou A, Draganidis D, et al. Short-term high-intensity interval exercise training attenuates oxidative stress responses and improves antioxidant status in healthy humans. Food Chem Toxicol 2013; 61: 171-7.
  8. Freitas DA, Rocha-Vieira E, Soares BA, Nonato LF, Fonseca SR, Martins JB, et al. High intensity interval training modulates hippocampal oxidative stress, BDNF and inflammatory mediators in rats. Physiol Behav 2018; 184: 6-11.
  9. Farinha JB, Ramis TR, Vieira AF, Macedo RCO, Rodrigues-Krause J, Boeno FP, et al. Glycemic, inflammatory and oxidative stress responses to different high-intensity training protocols in type 1 diabetes: A randomized clinical trial. J Diabetes Complications 2018; 32(12): 1124-32.
  10. Henke E, Oliveira VS, Silva IMd, Schipper L, Dorneles G, Elsner VR, et al. Acute and chronic effects of High Intensity Interval Training on inflammatory and oxidative stress markers of postmenopausal obese women. Transl Sports Med 2018; 1(6): 257-64.
  11. Mitranun W, Deerochanawong C, Tanaka H, Suksom D. Continuous vs interval training on glycemic control and macro- and microvascular reactivity in type 2 diabetic patients. Scand J Med Sci Sports 2014; 24(2): e69-e76.
  12. Wisloff U, Stoylen A, Loennechen JP, Bruvold M, Rognmo O, Haram PM, et al. Superior cardiovascular effect of aerobic interval training versus moderate continuous training in heart failure patients: A randomized study. Circulation 2007; 115(24): 3086-94.
  13. Inaba Y, Chen JA, Bergmann SR. Prediction of future cardiovascular outcomes by flow-mediated vasodilatation of brachial artery: a meta-analysis. Int J Cardiovasc Imaging 2010; 26(6): 631-40.
  14. Akbari H, Maleki MJ, Ravasi AA, Kordi MR, Dizagi A, Miri M, et al. The effect of an endurance training period with cellular Anti-aging purpose on telomerase enzyme activity in cardiac tissue and peripheral blood lymphocytes in male rats. J Med Counc I R Iran 2021; 31(4): 389-96. [In Persian].
  15. Akbari Bokani H, Ravasi AA, Akbari MR. The effect of a endurance training period with cellular anti-aging purpose on telomerase enzyme content in cardiac tissue and peripheral blood lymphocytes in rats. Sport Physiology and Management Investigations 2017; 9(3): 127-41. [In Persian].
  16. Mitchell SJ, Bernier M, Aon MA, Cortassa S, Kim EY, Fang EF, et al. Nicotinamide Improves Aspects of Healthspan, but Not Lifespan, in Mice. Cell Metab 2018; 27(3): 667-76.
  17. Kiss T, Balasubramanian P, Valcarcel-Ares MN, Tarantini S, Yabluchanskiy A, Csipo T, et al. Nicotinamide mononucleotide (NMN) treatment attenuates oxidative stress and rescues angiogenic capacity in aged cerebromicrovascular endothelial cells: a potential mechanism for the prevention of vascular cognitive impairment. Geroscience 2019; 41(5): 619-30.
  18. de Picciotto NE, Gano LB, Johnson LC, Martens CR, Sindler AL, Mills KF, et al. Nicotinamide mononucleotide supplementation reverses vascular dysfunction and oxidative stress with aging in mice. Aging Cell 2016; 15(3): 522-30.
  19. Bogan KL, Brenner C. Nicotinic acid, nicotinamide, and nicotinamide riboside: A molecular evaluation of NAD+ precursor vitamins in human nutrition. Annu Rev Nutr 2008; 28: 115-30.
  20. Sengupta P. The laboratory rat: Relating its age with human's. Int J Prev Med 2013; 4(6): 624-30.
  21. Uddin GM, Youngson NA, Doyle BM, Sinclair DA, Morris MJ. Nicotinamide mononucleotide (NMN) supplementation ameliorates the impact of maternal obesity in mice: comparison with exercise. Sci Rep 2017; 7(1): 15063.
  22. Bedford TG, Tipton CM, Wilson NC, Oppliger RA, Gisolfi CV. Maximum oxygen consumption of rats and its changes with various experimental procedures. J Appl Physiol Respir Environ Exerc Physiol 1979; 47(6): 1278-83.
  23. Linossier MT, Denis C, Dormois D, Geyssant A, Lacour JR. Ergometric and metabolic adaptation to a 5-s sprint training programme. Eur J Appl Physiol Occup Physiol 1993; 67(5): 408-14.
  24. Buege JA, Aust SD. Microsomal lipid peroxidation. Methods Enzymol 1978; 52: 302-10.
  25. Goudarzi M, Kalantari H, Rezaei M. Glyoxal toxicity in isolated rat liver mitochondria. Hum Exp Toxicol 2018; 37(5): 532-9.
  26. Han N, Shin JH, Han KH. An on-chip RT-PCR microfluidic device, that integrates mRNA extraction, cDNA synthesis, and gene amplification. Rsc Advances. 2014; 4(18): 9160-5.
  27. Ghorbanalipoor S, Ajami A, Rafiei AR, Taghvaei T, Paylakhi SH, Hosseini V. Expression of interleukin 11 (IL-11) in benign and malignant lesions of the gastric mucosa. J Mazand Univ Med Sci 2011; 21(84): 2-11. [In Persian].
  28. Namjoo E, Shekari M, Piruozi A, Forouzandeh H, Khalafkhany D, Vahedi A, et al. Haloperidol's effect on the expressions of TGFB, NT-3, and BDNF genes in cultured rat microglia. Basic Clin Neurosci 2020; 11(1): 49-58.
  29. Gorska P. Principles in laboratory animal research for experimental purposes. Med Sci Monit 2000; 6(1): 171-80.
  30. Rebelo-Marques A, De Sousa LA, Andrade R, Ribeiro CF, Mota-Pinto A, Carrilho F, et al. Aging hallmarks: The benefits of physical exercise. Front Endocrinol (Lausanne) 2018; 9: 258.
  31. Pham-Huy LA, He H, Pham-Huy C. Free radicals, antioxidants in disease and health. Int J Biomed Sci 2008; 4(2): 89-96.
  32. Halliwell B. Oxidative stress and neurodegeneration: Where are we now? J Neurochem 2006; 97(6): 1634-58.
  33. Droge W. Free radicals in the physiological control of cell function. Physiol Rev 2002; 82(1): 47-95.
  34. Senoner T, Dichtl W. Oxidative stress in cardiovascular diseases: still a therapeutic target? Nutrients 2019; 11(9): 2090.
  35. Lakshmi SV, Padmaja G, Kuppusamy P, Kutala VK. Oxidative stress in cardiovascular disease. Indian J Biochem Biophys 2009; 46(6): 421-40.
  36. Birben E, Sahiner UM, Sackesen C, Erzurum S, Kalayci O. Oxidative stress and antioxidant defense. World Allergy Organ J 2012; 5(1): 9-19.
  37. Hellsten Y, Apple FS, Sjodin B. Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle. J Appl Physiol (1985) 1996; 81(4): 1484-7.
  38. Csiszar A, Tarantini S, Yabluchanskiy A, Balasubramanian P, Kiss T, Farkas E, et al. Role of endothelial NAD(+) deficiency in age-related vascular dysfunction. Am J Physiol Heart Circ Physiol 2019; 316(6): H1253-H1266.
  • Receive Date: 26 January 2021
  • Revise Date: 25 May 2022
  • Accept Date: 22 May 2022