نوع مقاله : مقاله پژوهشی
نویسندگان
1 دکتری فیزیولوژی ورزشی، بخش علوم ورزشی، دانشکده علوم تربیتی وروانشناسی، دانشگاه شیراز، شیراز، ایران.
2 دانشیار بخش علوم ورزشی، دانشکده علوم تربیتی وروانشناسی، دانشگاه شیراز، شیراز، ایران.
3 استادیار بخش علوم ورزشی، دانشکده علوم تربیتی وروانشناسی، دانشگاه شیراز، شیراز، ایران.
چکیده
زمینه و هدف: پروتئین تنظیم کننده بیوژنز میتوکندریایی گیرنده فعال کننده تکثیر پروکسیزوم گاما-1 آلفا (PGC-1α) به عنوان عامل اصلی مسیر سیگنالینگ در کنترل متابولیسم میتوکندری عمل میکند. در عین حال، یک عامل رونویسی به نام عامل 2 وابسته به اریتروئید عامل هستهای-2 (Nrf2) نیز شناخته شده که با فعال سازی PGC-1α رابطه دارد و تا حدودی مشخص شده است که مسیر یکی از این دو عامل رونویسی، میتواند بر دیگری تأثیر بگذارد. هدف از تحقیق حاضر بررسی اثر هشت هفته تمرین مقاومتی به همراه مصرف مکملدهی کوآنزیم Q10 بر مقادیر Nrf2، PGC-1α در رتهای نر نژاد اسپراگوداولی بود. روش تحقیق: در این تحقیق تجربی، 36 سر رت به صورت تصادفی به شش گروه مساوی شامل گروه تمرین مقاومتی، دو گروه تمرین مقاومتی و مکمل Q10 با دوزهای 200 و 300 میلی گرم/کیلوگرم وزن، دو گروه مکمل Q10 با دوزهای 200 و 300 میلی گرم/کیلوگرم وزن، و کنترل تقسیم شدند. مکمل به رتها در گروههای تمرین - مکمل و مکمل، گاواژ شد. تمرین مقاومتی شامل سه نوبت با پنج تکرار بود که سه روز در هفته و به مدت هشت هفته اجرا گردید. از آزمونهای تحلیل واریانس یک راهه و توکی در سطح معنی داری 05/0>p برای استخراج نتایج استفاده شد. یافتهها: بیان Nrf2 و PGC-1α به طور معنیداری در گروههای تمرین مقاومتی و تمرین مقاومتی + مکمل (دوز 200 میلی گرم/کیلوگرم) افزایش یافت (0001>p)، در حالی که در گروه تمرین مقاومتی + مکمل با دوز 300 میلی گرم/کیلوگرم (07/0>p) و دو گروه دریافت کننده مکمل (09/0>p) تغییر معنیداری نکرد. نتیجه گیری: با توجه به اثر افزایشی ترکیب تمرینات مقاومتی همراه با مکمل دهی Q10 (با دوز 200 میلی گرم/کیلوگرم) در بهبود Nrf2 و PGC-1α؛ میتوان این شیوه را در بیوژنز میتوکندریایی موثر دانست.
کلیدواژهها
عنوان مقاله [English]
The effect of eight-weeks of resistance training a long with coenzyme Q10 supplementation on some factors of mitochondrial biogenesis in young male rats
نویسندگان [English]
- Mohammad Javad Shafahi 1
- Mohsen Salesi 2
- Rasoul Rezaei 3
- Farhad Daryanoosh 2
1 PhD in Exercise Physiology, Department of Sport Sciences, School of Education and Psychology, Shiraz University, Shiraz, Iran.
2 Associate Professor, Department of Sport Sciences, School of Education and Psychology, Shiraz University, Shiraz, Iran.
3 Assistant Professor of Exercise Physiology, Department of Sport Sciences, School of Education and Psychology, Shiraz University, Shiraz, Iran.
چکیده [English]
Background and Aim: The mitochondrial biogenesis-regulating protein of the peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) acts as a major signaling pathway for controlling of mitochondrial metabolism. Meanwhile, a transcription factor namely nuclear factor erythroid 2-related factor 2 (Nrf2) is recognized that also associated with PGC1α activation, and it has been shown to some extent to the pathway of one of these two transcription factors can affect the other. The aim of this study was to evaluate the effect of eight weeks of resistance training a long with coenzyme Q10 supplementation on Nrf2 and PGC-1α levels in male Sprague-Dawley rats. Materials and Methods: In this experimental study, 36 rats were randomly divided into six equal groups including resistance training, two resistance training and Q10 supplement (200 and 300 mg/kg/body weight), two supplement (200 and 300 mg/kg/body weight) and control group. The all supplements were applied as a gavage to the exercise-supplement and gavage supplement groups. Resistance training consisted of three sessions and five repetitions which were performed three days a week for eight weeks. One-way analysis of variance and Tukey tests at the significant level of p<0.05 were used to extract the results. Results: Nrf2 and PGC-1α expression increased significantly in resistance training and resistance training+supplement (200 mg/kg) groups (p<0001), while in resistance training group+supplement a dose of 300 mg/kg (p<0.07) and two groups of supplements (p<0.09) no significantly changes were observed. Conclusion: Due to the additive effect of resistance training combined with Q10 supplementation (a dose of 200 mg/kg) in improving Nrf2 and PGC-1α; it can be considered as a effective method in mitochondrial biogenesis.
کلیدواژهها [English]
- Resistance training
- Coenzyme Q10
- Nuclear factor erythroid 2-related factor 2
- Peroxisome proliferator-activated receptor gamma coactivator 1-alpha
Baar, K., Wende, A.R., Jones, T.E., Marison, M., Nolte, L.A., Chen, M.A.Y., & Holloszy, J. (2002). Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC‐1. The Federation of American Societies for Experimental Biology Journal, 16(14), 1879-1886.
Bentinger, M., Tekle, M., & Dallner, G. (2010). Coenzyme Q–biosynthesis and functions. Biochemical and Biophysical Research Communications, 396(1), 74-79.
Boccatonda, A., Tripaldi, R., Davì, G., & Santilli, F. (2016). Oxidative stress modulation through habitual physical activity. Current Pharmaceutical design, 22(24), 3648-3680.
Bryan, H.K., Olayanju, A., Goldring, C.E., & Park, B.K. (2013). The Nrf2 cell defence pathway: Keap1-dependent and-independent mechanisms of regulation. Biochemical Pharmacology, 85(6), 705-717.
Ebadi, M., Sharma, S.K., Wanpen, S., & Amornpan, A. (2004). Coenzyme Q10 inhibits mitochondrial complex‐1 down‐regulation and nuclear factor‐kappa B activation. Journal of Cellular and Molecular Medicine, 8(2), 213-222.
Garrido-Maraver, J., Cordero, M.D., Oropesa-Ávila, M., Vega, A.F., De La Mata, M., Pavón, A.D., & Sánchez-Alcázar, J.A. (2014). Coenzyme q10 therapy. Molecular Syndromology, 5(3-4), 187-197.
Gounder, S.S., Kannan, S., Devadoss, D., Miller, C.J., Whitehead, K.S., Odelberg, S.J., & Rajasekaran, N.S. (2012). Impaired transcriptional activity of Nrf2 in age-related myocardial oxidative stress is reversible by moderate exercise training. Journal of Scientific Exploration, 7(9), e45697.
Granata, C., Jamnick, N.A., & Bishop, D.J. (2018). Principles of exercise prescription, and how they influence exercise- induced changes of transcription factors and other regulators of mitochondrial biogenesis. Sports Medicine, 48(7), 1541-1559.
Handy, D.E., & Loscalzo, J. (2012). Redox regulation of mitochondrial function. Antioxidants & Redox Signaling, 16(11), 1323-1367.
Hong, D.S., Kurzrock, R., Supko, J.G., He, X., Naing, A., Wheler, J., & Dezube, B.J. (2012). A phase I first-in-human trial of bardoxolone methyl in patients with advanced solid tumors and lymphomas. Clinical Cancer Research, 18(12), 3396-3406.
Kansanen, E., Kuosmanen, S.M., Leinonen, H., & Levonen, A.L. (2013). The Keap1-Nrf2 pathway: Mechanisms of activation and dysregulation in cancer. Redox Biology, 1(1), 45-49.
Kon, M., Kimura, F., Akimoto, T., Tanabe, K., Murase, Y., Ikemune, S., & Kono, I. (2007). Effect of coenzyme Q10 supplementation on exercise-induced muscular injury of rats. Exercise Immunology, 13(2), 76-88.
Lin, J., Handschin, C., & Spiegelman, B.M. (2005). Metabolic control through the PGC-1 family of transcription coactivators. Cell Metabolism, 1(6), 361-370.
Merry, T. L., & Ristow, M. (2016). Nuclear factor erythroid‐derived 2‐like 2 (NFE2L2, Nrf2) mediates exercise‐induced mitochondrial biogenesis and the anti‐oxidant response in mice. The Journal of Physiology, 594(18), 5195-5207.
Pala, R., Orhan, C., Tuzcu, M., Sahin, N., Ali, S., Cinar, V., ... & Sahin, K. (2016). Coenzyme Q10 supplementation modulates NFκB and Nrf2 pathways in exercise training. Journal of Sports Science & Medicine, 15(1), 196.
Powers, S.K., & Jackson, M.J. (2008). Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiological Reviews, 88(4), 1243-1276.
Raghunath, A., Sundarraj, K., Nagarajan, R., Arfuso, F., Bian, J., Kumar, A.P., ... & Perumal, E. (2018). Antioxidant response elements: discovery, classes, regulation and potential applications. Redox Biology, 17(6), 297-314.
Samavati Sharif, M.A., Afshar, A., Siavoshy, H., & Keshvary, M. (2017). The effect of two exercises training on some of immune system markers in adolescent athletes. Journal of Practical Studies of Biosciences in Sport, 4(8), 55-65. [In Persian]
Scarpulla, R.C. (2008). Nuclear control of respiratory chain expression by nuclear respiratory factors and PGC-1-related coactivator. Annals of The New York Academy of Sciences, 4(11), 345-367.
Scarpulla, R.C. (2018). Transcriptional paradigms in mammalian mitochondrial biogenesis and function. Physiological reviews, 88(2), 611-638.
Su, X., Jiang, X., Meng, L., Dong, X., Shen, Y., & Xin, Y. (2018). Anticancer activity of sulforaphane: the epigenetic mechanisms and the Nrf2 signaling pathway. Oxidative Medicine and Cellular Longevity, 16(11), 1345-1367.
Sun, Z., Zhang, S., Chan, J.Y., & Zhang, D.D. (2007). Keap1 controls postinduction repression of the Nrf2-mediated antioxidant response by escorting nuclear export of Nrf2. Molecular and Cellular Biology, 27(18), 6334-6349.
Tebay, L.E., Robertson, H., Durant, S.T., Vitale, S.R., Penning, T.M., Dinkova-Kostova, A.T., & Hayes, J.D. (2015). Mechanisms of activation of the transcription factor Nrf2 by redox stressors, nutrient cues, and energy status and the pathways through which it attenuates degenerative disease. Free Radical Biology and Medicine, 88(6), 108-146.
Vargas-Mendoza, N., Morales-González, Á., Madrigal-Santillán, E.O., Madrigal-Bujaidar, E., Álvarez-González, I., García-Melo, L.F., & Morales-Gonzalez, J.A. (2019). Antioxidant and adaptative response mediated by Nrf2 during physical exercise. Antioxidants, 8(6), 196.
Vomund, S., Schäfer, A., Parnham, M.J., Brüne, B., & Von Knethen, A. (2017). Nrf2, the master regulator of anti-oxidative responses. International Journal of Molecular Sciences, 18(12), 27-32.
Wang, P., Li, C.G., Qi, Z., Cui, D., & Ding, S. (2016). Acute exercise stress promotes Ref1/Nrf2 signalling and increases mitochondrial antioxidant activity in skeletal muscle. Experimental Physiology, 101(3), 410-420.
Zhang, Y.P., Song, C.Y., Yuan, Y., Eber, A., Rodriguez, Y., Levitt, R.C., & Candiotti, K.A. (2013). Diabetic neuropathic pain development in type 2 diabetic mouse model and the prophylactic and therapeutic effects of coenzyme Q10. Neurobiology of Disease, 58(1), 169-178.