ورزش و علوم زیست حرکتی

ورزش و علوم زیست حرکتی

تاثیر 8 هفته تمرینات تناوبی شنا با شدت بالا بر سطح فاکتور شبه هسته‌ای ۲ مشتق از اریتروئید ۲ (Nrf2) و سوپراکسیددیسموتاز (SOD) در موش های صحرایی نر چاق مبتلا به استئاتوهپاتیت غیرالکلی

نویسندگان
1 موسسه آموزش عالی زند شیراز
2 دانشگاه شیراز
چکیده
مقدمه و هدف: با افزایش بی­ تحرکی در دنیای مدرن امروزی، بسیاری از بیماری­ های متابولیکی ناشی از عدم فعالیت بدنی گسترش یافته­ اند. از جمله این بیماری­ ها می­ توان به بیماری استئاتوهپاتیت غیرالکلی اشاره کرد که با افزایش استرس اکسیداتیو همراه است. هدف از این پژوهش، بررسی تاثیر هشت هفته تمرینات تناوبی شنا با شدت بالا بر سطح فاکتور شبه­ هسته‌ای ۲ مشتق از اریتروئید ۲ (Nrf2) و سوپراکسید­دیسموتاز (SOD) در موش­ های صحرایی نر چاق مبتلا به استئاتوهپاتیت غیرالکلی (NASH) بود.
مواد و روش ­ها: در ابتدا موش­ های صحرایی در سن 6 تا 8 هفته به­ طور تصادفی به دو گروه سالم (20= n) و بیمار (رژیم پرچرب (HFD)) (n=20) تقسیم شدند. رژیم پرچرب به مدت 8 هفته ادامه داشت تا موش­ه ای صحرایی مبتلا به NASH شوند. پس از القا بیماری، گروه بیمار به­ طور تصادفی به 2 گروه بیمار - بی­ تحرک (10=n)، بیمار - شنا (10=n)،  تقسیم شدند؛ هم­چنین گروه سالم نیز به دو گروه سالم - بی­ تحرک (10=n) و گروه سالم - شنا (10=n) تقسیم گردیدند. تمرین HIIT شنا، شامل 20 نوبت 30 ثانیه ­ای شنا با 30 ثانیه استراحت بین هر نوبت (سه روز در هفته به مدت هشت هفته) بود. در تمرین تناوبی، بار اعمال شده در هفته اول، وزنه­ ای به میزان 7 درصد وزن بدن هر موش صحرایی بود و هر هفته 1 درصد به آن اضافه شد. پروتئین Nrf2 از بافت کبد و از طریق تکنیک وسترن بلات و SOD از سرم خون اندازه ­گیری شدند. برای مشخص نمودن تفاوت میان گروه­ ها از آزمون آماری آنووای یکراهه و آزمون تعقیبی بونفرونی (0.05>P < span lang="FA">) استفاده شد.
یافته‌ها: نتایج آنالیز آماری نشان داد در متغیر SOD، گروه بیمار بی­تحرک نسبت به سالم بی­ تحرک و سالم - شنا کاهش معنادار (0.05>P < span lang="FA">) و گروه سالم - شنا نسبت به بیمار - شنا افزایش معنادار وجود داشت (0.05>P < span lang="FA">). در متغیر Nrf2 گروه سالم - بی­ تحرک نسبت به گروه ­های بیمار - بی­ تحرک و بیمار - شنا افزایش معنادار وجود داشت (0.05>P < span lang="FA">). هم­چنین در گروه بیمار - شنا نسبت به بیمار - بی­ تحرک تغییر معناداری وجود نداشت(0.05
)
بحث و نتیجه­ گیری: تمرینات تناوبی شنا با شدت بالا در بیماران مبتلا به NASH، می­تواند بر سیستم آنتی­ اکسیدانی تاثیر مثبت داشته باشد با این­ وجود در این زمینه انجام پژوهش­ های دیگر ضروری است.
کلیدواژه‌ها

عنوان مقاله English

The effect of 8 weeks of high-intensity swimming interval training on the factor level of Erythroid-Derived 2-nuclear Factor 2 (Nrf2) and Superoxide Dismutase (SOD) in obese male rats with Non-alcoholic Steatohepatitis

نویسندگان English

Mohammad Hashemi Azizli 1
Farhad Daryanoosh 2
Homa Sheikhani Shahin 1
Alireza Jowhari 2
چکیده English

Introduction and purpose: With the increase of inactivity in today's modern world, many metabolic diseases caused by lack of physical activity have spread. Among these diseases, we can mention non-alcoholic steatohepatitis, which is associated with increased oxidative stress. This study aimed to investigate the effect of 8 weeks of high-intensity swimming interval training on the factor level of Erythroid-Derived 2-Nuclear Factor 2 (Nrf2) and superoxide dismutase (SOD) in obese male rats with non-alcoholic Steatohepatitis (NASH).
Material and methods: At the beginning, rats aged 6 to 8 years were randomly divided into healthy (n=20) and sick (high fat diet (HFD)) (n=20) groups. The high-fat diet lasted eight weeks until the rats became infected with NASH. After induction of the disease, the patient group was divided into 2 groups: disease-immobile (n=10), disease-swimming (n=10) by chance; Also, the healthy group was divided into two groups: healthy-immobile (n=10) and healthy-swimming (n=10). The HIIT swimming exercise consisted of 20 30-second swimming sessions with a 30-second break between sessions (three days a week for eight weeks). In the interval training load applied in the first week, a weight of 7% of each rat's body weight added, and 1% added to it every week. Nrf2 protein measured from liver tissue through the western blotting technique and SOD from blood serum. One-way ANOVA and Bonferroni post hoc test (p<0.05) were used to determine the differences between the groups.
Results: The results of statistical analysis showed that in the SOD variable, there was a significant decrease (P<0.05) in the inactive disease group compared to the sedentary and sedentary healthy group and a significant increase in the healthy-swimming group compared to the patient-swimming group (P<0.05). There was a significant increase in the Nrf2 variable of the healthy-inactive group compared to the patient-inactive and disease-swimming groups (P<0.05). There was also a non-significant increase in the disease-swimming group compared to the patient-immobile
Discussion and Conclusion: high-intensity swimming interval training in patients with NASH can have a positive effect on the anti-oxidant system, but it is necessary to conduct other research.
Key words: Erythroid-Derived 2-Nuclear Factor 2, Superoxide Dismutase, High-intensity swimming interval training, Non-alcoholic Steatohepatitis

کلیدواژه‌ها English

Erythroid-Derived 2-Nuclear Factor 2 (Nrf2)
Superoxide dismutase (SOD)
high-intensity swimming interval training
Non-alcoholic Steatohepatitis (NASH)
1. Vernon G, Baranova A, Younossi Z. Systematic review: the epidemiology and natural history of non‐alcoholic fatty liver disease and non‐alcoholic steatohepatitis in adults. Alimentary pharmacology & therapeutics. 2011;34(3):274-85. 2. Roeb E, Geier A. Nonalcoholic steatohepatitis (NASH)–current treatment recommendations and future developments. Zeitschrift für Gastroenterologie. 2019;57(04):508-17. 3. Rosato V, Masarone M, Dallio M, Federico A, Aglitti A, Persico M. NAFLD and extra-hepatic comorbidities: current evidence on a multi-organ metabolic syndrome. International journal of environmental research and public health. 2019;16(18):3415. 4. Polimeni L, Del Ben M, Baratta F, Perri L, Albanese F, Pastori D, et al. Oxidative stress: New insights on the association of non-alcoholic fatty liver disease and atherosclerosis. World journal of hepatology. 2015;7(10):1325. 5. Farzanegi P, Dana A, Ebrahimpoor Z, Asadi M, Azarbayjani MA. Mechanisms of beneficial effects of exercise training on non-alcoholic fatty liver disease (NAFLD): Roles of oxidative stress and inflammation. European journal of sport science. 2019;19(7):994-1003. 6. Hajighasem A, Farzanegi P, Mazaheri Z. Effects of combined therapy with resveratrol, continuous and interval exercises on apoptosis, oxidative stress, and inflammatory biomarkers in the liver of old rats with non-alcoholic fatty liver disease. Archives of physiology and biochemistry. 2019;125(2):142-9. 7. Ding C, Zhao Y, Shi X, Zhang N, Zu G, Li Z, et al. New insights into salvianolic acid A action: Regulation of the TXNIP/NLRP3 and TXNIP/ChREBP pathways ameliorates HFD-induced NAFLD in rats. Scientific reports. 2016;6:28734. 8. Krautbauer S, Eisinger K, Lupke M, Wanninger J, Ruemmele P, Hader Y, et al. Manganese superoxide dismutase is reduced in the liver of male but not female humans and rodents with non-alcoholic fatty liver disease. Experimental and molecular pathology. 2013;95(3):330-5. 9. Tonelli C, Chio IIC, Tuveson DA. Transcriptional regulation by Nrf2. Antioxidants & redox signaling. 2018;29(17):1727-45. 10. Vargas-Mendoza N, Morales-González Á, Madrigal-Santillán EO, Madrigal-Bujaidar E, Álvarez-González I, García-Melo LF, et al. Antioxidant and Adaptative Response Mediated by Nrf2 during Physical Exercise. Antioxidants. 2019;8(6):196. 11. Wang P, Li CG, Qi Z, Cui D, Ding S. Acute exercise stress promotes Ref1/Nrf2 signalling and increases mitochondrial antioxidant activity in skeletal muscle. Experimental physiology. 2016;101(3):410-20. 12. Li T, He S, Liu S, Kong Z, Wang J, Zhang Y. Effects of different exercise durations on Keap1-Nrf2-ARE pathway activation in mouse skeletal muscle. Free radical research. 2015;49(10):1269-74. 13. Ostrom EL, Valencia AP, Marcinek DJ, Traustadóttir T. High intensity muscle stimulation activates a systemic Nrf2-mediated redox stress response. Free Radical Biology and Medicine. 2021;172:82-9. 14. Done AJ, Traustadóttir T. Nrf2 mediates redox adaptations to exercise. Redox biology. 2016;10:191-9. 15. Younossi ZM, Blissett D, Blissett R, Henry L, Stepanova M, Younossi Y, et al. The economic and clinical burden of nonalcoholic fatty liver disease in the United States and Europe. Hepatology. 2016;64(5):1577-86. 16. Brunner KT, Henneberg CJ, Wilechansky RM, Long MT. Nonalcoholic fatty liver disease and obesity treatment. Current obesity reports. 2019;8(3):220-8. 17. Patel NS, Doycheva I, Peterson MR, Hooker J, Kisselva T, Schnabl B, et al. Effect of weight loss on magnetic resonance imaging estimation of liver fat and volume in patients with nonalcoholic steatohepatitis. Clinical gastroenterology and hepatology. 2015;13(3):561-8. e1. 18. Marchesini G, Petta S, Dalle Grave R. Diet, weight loss, and liver health in nonalcoholic fatty liver disease: Pathophysiology, evidence, and practice. Hepatology. 2016;63(6):2032-43. 19. Chalasani N, Younossi Z, Lavine JE, Charlton M, Cusi K, Rinella M, et al. The diagnosis and management of nonalcoholic fatty liver disease: practice guidance from the American Association for the Study of Liver Diseases. Hepatology. 2018;67(1):328-57. 20. Zelber-Sagi S, Buch A, Yeshua H, Vaisman N, Webb M, Harari G, et al. Effect of resistance training on non-alcoholic fatty-liver disease a randomized-clinical trial. World journal of gastroenterology: WJG. 2014;20(15):4382. 21. Nagle EF, Sanders ME, Franklin BA. Aquatic high intensity interval training for cardiometabolic health: benefits and training design. American Journal of Lifestyle Medicine. 2017;11(1):64-76. 22. Martins RR, de Oliveira Macedo UB, Leite LD, Rezende AA, Brandão-Neto J, Almeida MdG. Lipoic acid and moderate swimming improves the estrous cycle and oxidative stress in Wistar rats. Applied physiology, nutrition, and metabolism. 2011;36(5):693-7. 23. Zou Y, Li J, Lu C, Wang J, Ge J, Huang Y, et al. High-fat emulsion-induced rat model of nonalcoholic steatohepatitis. Life sciences. 2006;79(11):1100-7. 24. Farzanegi P, habibian m, alinejad h. The Combined Effect of Regular Aerobic Exercise with Garlic Extract on Renal Apoptosis Regulatory Factors in Aged rats with Chronic Kidney Disease. Journal of Arak University of Medical Sciences. 2016;19(3):62-70. 25. Ramos-Filho D, Chicaybam G, de-Souza-Ferreira E, Guerra Martinez C, Kurtenbach E, Casimiro-Lopes G, et al. High intensity interval training (HIIT) induces specific changes in respiration and electron leakage in the mitochondria of different rat skeletal muscles. PloS one. 2015;10(6):e0131766. 26. Shafiee A, Gaeini A, Soleimani M, Nekouei A, Hadidi V. The effect of eight week of high intensity interval training on expression of mir-210 and ephrinA3 mRNA in soleus muscle healthy male rats. Journal of Arak University of Medical Sciences. 2014;17(3):26-34. 27. Skandari M, Nazemzadegan GH, Daryanosh F, Samadi M, Honarpisheh S, Hasanpor M. Comparative effect of single bout of continuous endurance and high intensity interval exercise on serum BDNF in rat. KAUMS Journal (FEYZ). 2016;20(2):141-6. 28. Alouie A, Zehsaz F, Pouzesh Jadidi R. Effect of endurance exercise with chamomile recutita leaves extract on liver superoxide dismutase activity and malondialdehyde levels in type 1 diabetic rats. Research in Medicine. 2017;40(4):165-71. 29. Mohammad Hosseini F, Hosseini SA, Ahmadi M. The effect of a period of swimming training and chamomile extract on antioxidant status in adult male rats. Qom University of Medical Sciences Journal. 2018;12(6):10-9. 30. Nonato L, Rocha-Vieira E, Tossige-Gomes R, Soares A, Soares B, Freitas D, et al. Swimming training attenuates oxidative damage and increases enzymatic but not non-enzymatic antioxidant defenses in the rat brain. Brazilian Journal of Medical and Biological Research. 2016;49. 31. Casimiro-Lopes G, Ramos D, Sorenson MM, Salerno VP. Redox balance and mitochondrial glycerol phosphate dehydrogenase activity in trained rats. European journal of applied physiology. 2012;112(11):3839-46. 32. Benzie IF, Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Analytical biochemistry. 1996;239(1):70-6. 33. Nazem F, Farhangi N, Neshat-Gharamaleki M. Beneficial effects of endurance exercise with Rosmarinus officinalis labiatae leaves extract on blood antioxidant enzyme activities and lipid peroxidation in streptozotocin-induced diabetic rats. Canadian journal of diabetes. 2015;39(3):229-34. 34. Peeri M, Haghigh MM, Azarbayjani MA, Atashak S, Behrouzi G. Effect of aqueous extract of saffron and aerobic training on hepatic non enzymatic antioxidant levels in streptozotocin-diabetic rats. Archives Des Sciences. 2012;65(10):525-32. 35. Henkel J, Buchheim-Dieckow K, Castro JP, Laeger T, Wardelmann K, Kleinridders A, et al. Reduced oxidative stress and enhanced FGF21 formation in livers of endurance-exercised rats with diet-induced NASH. Nutrients. 2019;11(11):2709. 36. Keihanian A, Arazi H, Kargarfard M. Effects of aerobic versus resistance training on serum fetuin-A, fetuin-B, and fibroblast growth factor-21 levels in male diabetic patients. Physiology International. 2019;106(1):70-80. 37. Gonzalez A, Huerta-Salgado C, Orozco-Aguilar J, Aguirre F, Tacchi F, Simon F, et al. Role of oxidative stress in hepatic and extrahepatic dysfunctions during nonalcoholic fatty liver disease (NAFLD). Oxidative Medicine and Cellular Longevity. 2020;2020. 38. Coskun O, Ocakci A, Bayraktaroglu T, Kanter M. Exercise training prevents and protects streptozotocin-induced oxidative stress and β-cell damage in rat pancreas. The Tohoku journal of experimental medicine. 2004;203(3):145-54. 39. Zou Y, Chen Z, Sun C, Yang D, Zhou Z, Peng X, et al. Exercise Intervention Mitigates Pathological Liver Changes in NAFLD Zebrafish by Activating SIRT1/AMPK/NRF2 Signaling. International journal of molecular sciences. 2021;22(20):10940.
دوره 13، شماره 26 - شماره پیاپی 26
پاییز و زمستان
اسفند 1400
صفحه 66-76

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