تأثیر مکمل بتا-هیدروکسی-β-متیل بوتیرات بر IL-4، IL-10 و TGF-β1 در طول ورزش مقاومتی در ورزشکاران

نوع مقاله : مقاله پژوهشی Released under (CC BY-NC 4.0) license I Open Access I

نویسندگان

1 دانشیار فیزیولوژی ورزشی، گروه فیزیولوژی ورزشی، دانشکده علوم انسانی و اجتماعی، دانشگاه کردستان، سنندج، کردستان، ایران.

2 کارشناسی ارشد فیزیولوژی ورزشی، گروه فیزیولوژی ورزشی، دانشکده علوم انسانی و اجتماعی، دانشگاه کردستان، سنندج، کردستان، ایران.

چکیده

هدف از این مطالعه بررسی تأثیر مکمل بتا-هیدروکسی-β-متیل بوتیرات (HMB) بر سیتوکین‌های ضد التهابی شامل IL-4، IL-10 و TGF-β در طول یک جلسه تمرین مقاومتی حاد (RE) در مردان جوان تمرین کرده با تمرینات مقاومتی بود. ده مرد تمرین کرده با تمرینات مقاومتی در یک مطالعه تصادفی، دوسوکور، کنترل شده با دارونما و متقاطع، به مدت 7 روز مکمل HMB (3×1 گرم در روز HMB) و دارونما (3×1 گرم در روز مالتودکسترین) با یک دوره استراحت 7 روزه دریافت کردند. پس از دوره‌های مکمل، آزمودنی‌ها سه ست پرس سینه، کشش لت به پایین، جلو پا، پشت پا، جلو بازو، جلو بازو، جلو بازو، جلو بازو و پرس شانه تا حد ناتوانی با 85٪ از یک تکرار بیشینه (1RM) انجام دادند. نمونه‌های خون قبل (قبل)، بلافاصله پس از (IP) و 1 ساعت پس از RE (1 ساعت P) برای ارزیابی غلظت سرمی IL-4، IL-10 و TGF-β1 گرفته شد. داده‌ها با استفاده از تحلیل واریانس با اندازه‌گیری‌های مکرر (ANOVA) 2 (تیمار: HMB و PL) × 3 (نقاط زمانی: قبل، قبل و بعد از 1 ساعت تمرین) و به دنبال آن آزمون تعقیبی بونفرونی با سطح معنی‌داری p<0.05 تجزیه و تحلیل شدند. IL-4 سرم در تمرین مقاومتی IP در HMB در مقایسه با دارونما به طور معنی‌داری بالاتر بود. IL-4 و TGF-β1 در گردش خون در IP در مقایسه با قبل در هر دو گروه HMB و دارونما به طور معنی‌داری افزایش یافت. هیچ تفاوت معنی‌داری بین تیمارها برای IL-10 و TGF-β1 در هیچ یک از نقاط زمانی مشاهده نشد. در نتیجه، مکمل HMB سطح IL-4 در گردش خون را در طول RE در مردان تمرین کرده با مقاومت افزایش داد، که ممکن است التهاب را کاهش داده و سازگاری با RE را تسهیل کند.

تازه های تحقیق

 

کلیدواژه‌ها


عنوان مقاله [English]

Effects of β-Hydroxy-β-Methylbutyrate Supplementation on IL-4, IL-10 and TGF-β1 during Resistance Exercise in Athletes

نویسندگان [English]

  • Mohammad Rahman Rahimi 1
  • Hamid Shoker-Nejad 2
1 Associate Professor of Exercise Physiology, Department of Exercise Physiology, Faculty of Humanities and Social Sciences, University of Kurdistan, Sanandaj, Kurdistan, Iran.
2 Master of exercise physiology, Department of Exercise Physiology, Faculty of Humanities and Social Sciences, University of Kurdistan, Sanandaj, Kurdistan, Iran.
چکیده [English]

The aim of this study was to investigate the effect of β-Hydroxy-β-methylbutyrate (HMB) supplementation on anti-inflammatory cytokines including IL-4, IL-10 and TGF-β during an acute bout of resistance exercise (RE) in young resistance trained men. Ten resistance-trained men in a randomized, double-blind, placebo-controlled and crossover study, were administered a 7-day HMB supplementation (3×1 g.d-1 of HMB) and placebo (3×1 g.d-1 of Maltodextrin) with a 7 days washout period. After supplementation periods, subjects performed three sets of bench press, lat pull down, leg extension, leg curl, biceps curl, triceps curl and shoulder press to failure with 85% of one repetition to maximum (1RM). Blood samples were obtained before- (Pre), immediately post- (IP) and 1 hour-post RE (1h P) to assess serum concentrations of IL-4, IL-10 and TGF-β1. The data were analyzed using 2 (treatment: HMB and PL) × 3 (time points: Pre, IP and 1hP) repeated measures analysis of variance (ANOVA) followed by the Bonferroni post hoc test with a significant level of p<0.05. Serum IL-4 was significantly higher at IP resistance exercise in HMB compared to placebo. Circulating IL-4 and TGF-β1 were significantly raised at IP compared to Pre in both HMB and placebo treatments. No significant differences between treatments were observed for IL-10 and TGF-β1at any time points. In conclusion, HMB supplementation increased the circulating level of IL-4 during RE in resistance-trained men, which may attenuate inflammation and facilitate adaptation to RE.

کلیدواژه‌ها [English]

  • β-Hydroxy-β-Methylbutyrate
  • anti-inflamatory cytokines
  • resistance exercise

 

[1] N. Mathur, B.K. Pedersen, Exercise as a mean to control low-grade systemic inflammation, Mediators of inflammation 2008 (2009).
[2] T.W. Buford, M.B. Cooke, D.S. Willoughby, Resistance exercise-induced changes of inflammatory gene expression within human skeletal muscle, European journal of applied physiology 107(4) (2009) 463.
[3] M.C. Calle, M.L. Fernandez, Effects of resistance training on the inflammatory response, Nutrition research and practice 4(4) (2010) 259-269.
[4] A.M.W. Petersen, B.K. Pedersen, The anti-inflammatory effect of exercise, Journal of applied physiology 98(4) (2005) 1154-1162.
[5] L. Smith, A. Anwar, M. Fragen, C. Rananto, R. Johnson, D. Holbert, Cytokines and cell adhesion molecules associated with high-intensity eccentric exercise, European journal of applied physiology 82(1-2) (2000) 61-67.
[6] J.R. Townsend, M.S. Fragala, A.R. Jajtner, A.M. Gonzalez, A.J. Wells, G.T. Mangine, E.H. Robinson, W.P. McCormack, K.S. Beyer, G.J. Pruna, β-Hydroxy-β-methylbutyrate (HMB)-free acid attenuates circulating TNF-α and TNFR1 expression postresistance exercise, Journal of Applied Physiology 115(8) (2013) 1173-1182.
[7] M.C. Uchida, K. Nosaka, C. Ugrinowitsch, A. Yamashita, E. Martins Jr, A.S. Moriscot, M.S. Aoki, Effect of bench press exercise intensity on muscle soreness and inflammatory mediators, Journal of sports sciences 27(5) (2009) 499-507.
[8] M. Sousa, V.H. Teixeira, J. Soares, Dietary strategies to recover from exercise-induced muscle damage, International journal of food sciences and nutrition 65(2) (2014) 151-163.
[9] S. Arbogast, M.B. Reid, Oxidant activity in skeletal muscle fibers is influenced by temperature, CO2 level, and muscle-derived nitric oxide, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 287(4) (2004) R698-R705.
[10] B.K. Pedersen, L. Hoffman-Goetz, Exercise and the immune system: regulation, integration, and adaptation, Physiological reviews 80(3) (2000) 1055-1081.
[11] S.K. Powers, M.J. Jackson, Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production, Physiological reviews 88(4) (2008) 1243-1276.
[12] M. Gleeson, N.C. Bishop, D.J. Stensel, M.R. Lindley, S.S. Mastana, M.A. Nimmo, The anti-inflammatory effects of exercise: mechanisms and implications for the prevention and treatment of disease, Nature reviews. Immunology 11(9) (2011) 607.
[13] D.C. Kluth, A.J. Rees, Inhibiting inflammatory cytokines, Seminars in nephrology, 1996, pp. 576-582.
[14] S.M. Opal, V.A. DePalo, Anti-inflammatory cytokines, Chest Journal 117(4) (2000) 1162-1172.
[15] K.A. Volaklis, I. Smilios, A.T. Spassis, C.E. Zois, H.T. Douda, M. Halle, S.P. Tokmakidis, Acute pro-and anti-inflammatory responses to resistance exercise in patients with coronary artery disease: a pilot study, Journal of sports science & medicine 14(1) (2015) 91.
[16] J.M. Wilson, R.P. Lowery, J.M. Joy, J.A. Walters, S.M. Baier, J.C. Fuller, J.R. Stout, L.E. Norton, E.M. Sikorski, S.M. Wilson, β-Hydroxy-β-methylbutyrate free acid reduces markers of exercise-induced muscle damage and improves recovery in resistance-trained men, British Journal of Nutrition 110(03) (2013) 538-544.
[17] W.J. Kraemer, D.L. Hatfield, B.A. Comstock, M.S. Fragala, P.M. Davitt, C. Cortis, J.M. Wilson, E.C. Lee, R.U. Newton, C. Dunn-Lewis, Influence of HMB supplementation and resistance training on cytokine responses to resistance exercise, Journal of the American College of Nutrition 33(4) (2014) 247-255.
[18] W.J. Kraemer, D.R. Hooper, T.K. Szivak, B.R. Kupchak, C. Dunn-Lewis, B.A. Comstock, S.D. Flanagan, D.P. Looney, A.J. Sterczala, W.H. DuPont, The addition of beta-hydroxy-beta-methylbutyrate and isomaltulose to whey protein improves recovery from highly demanding resistance exercise, Journal of the American College of Nutrition 34(2) (2015) 91-99.
[19] D.S. Rowlands, J.S. Thomson, Effects of β-hydroxy-β-methylbutyrate supplementation during resistance training on strength, body composition, and muscle damage in trained and untrained young men: A meta-analysis, The Journal of Strength & Conditioning Research 23(3) (2009) 836-846.
[20] E.A. Nunes, A.R. Lomax, P.S. Noakes, E.A. Miles, L.C. Fernandes, P.C. Calder, β-Hydroxy-β-methylbutyrate modifies human peripheral blood mononuclear cell proliferation and cytokine production in vitro, Nutrition 27(1) (2011) 92-99.
[21] J. Hoffman, Norms for fitness, performance, and health, Human Kinetics2006.
[22] A. Marchant, C. Bruyns, P. Vandenabeele, M. Ducarme, C. Gérard, A. Delvaux, D. De Groote, D. Abramowicz, T. Velu, M. Goldman, Interleukin‐10 controls interferon‐γ and tumor necrosis factor production during experimental endotoxemia, European journal of immunology 24(5) (1994) 1167-1171.
[23] V. Horsley, K.M. Jansen, S.T. Mills, G.K. Pavlath, IL-4 acts as a myoblast recruitment factor during mammalian muscle growth, Cell 113(4) (2003) 483-494.
[24] A.M. Gonzalez, J.R. Stout, A.R. Jajtner, J.R. Townsend, A.J. Wells, K.S. Beyer, C.H. Boone, G.J. Pruna, G.T. Mangine, T.M. Scanlon, Effects of β-hydroxy-β-methylbutyrate free acid and cold water immersion on post-exercise markers of muscle damage, Amino acids 46(6) (2014) 1501-1511.
[25] A.M. Gonzalez, M.S. Fragala, A.R. Jajtner, J.R. Townsend, A.J. Wells, K.S. Beyer, C.H. Boone, G.J. Pruna, G.T. Mangine, J.D. Bohner, Effects of β-hydroxy-β-methylbutyrate free acid and cold water immersion on expression of CR3 and MIP-1β following resistance exercise, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 306(7) (2014) R483-R489.
[26] J.R. Hoffman, Y. Gepner, J.R. Stout, M.W. Hoffman, D. Ben-Dov, S. Funk, I. Daimont, A.R. Jajtner, J.R. Townsend, D.D. Church, β-Hydroxy-β-methylbutyrate attenuates cytokine response during sustained military training, Nutrition Research 36(6) (2016) 553-563.
[27] S. Portal, A. Eliakim, D. Nemet, O. Halevy, Z. Zadik, Effect of HMB supplementation on body composition, fitness, hormonal profile and muscle damage indices, Journal of Pediatric Endocrinology and Metabolism 23(7) (2010) 641-650.
[28] S.M. Opal, J.C. Wherry, P. Grint, Interleukin-10: potential benefits and possible risks in clinical infectious diseases, Clinical infectious diseases 27(6) (1998) 1497-1507.
[29] Yan Wang, Research progress of relations between exercise training and obese chronic inflammatory, Journal of Chemical & Pharmaceutical Research 5(2) (2013) 829.
[30] D.C. Nieman, N.C. Bishop, Nutritional strategies to counter stress to the immune system in athletes, with special reference to football, Journal of sports sciences 24(07) (2006) 763-772.
[31] D.C. Nieman, D.A. Henson, J.M. Davis, E.A. Murphy, D.P. Jenkins, S.J. Gross, M.D. Carmichael, J.C. Quindry, C.L. Dumke, A.C. Utter, Quercetin's influence on exercise-induced changes in plasma cytokines and muscle and leukocyte cytokine mRNA, Journal of Applied Physiology 103(5) (2007) 1728-1735.
[32] D.C. Nieman, J.M. Davis, D.A. Henson, J. Walberg-Rankin, M. Shute, C.L. Dumke, A.C. Utter, D.M. Vinci, J.A. Carson, A. Brown, Carbohydrate ingestion influences skeletal muscle cytokine mRNA and plasma cytokine levels after a 3-h run, Journal of applied physiology 94(5) (2003) 1917-1925.
[33] A.V. Caris, E.T. Da Silva, S.A. Dos Santos, F.S. Lira, L.M. Oyama, S. Tufik, R.V.T. Dos Santos, Carbohydrate Supplementation Influences Serum Cytokines after Exercise under Hypoxic Conditions, Nutrients 8(11) (2016) 706.
[34] L. Hirose, K. Nosaka, M. Newton, A. Laveder, M. Kano, J. Peake, K. Suzuki, Changes in inflammatory mediators following eccentric exercise of the elbow flexors, Exerc Immunol Rev 10(75-90) (2004) 20.
[35] P.A. Della Gatta, A.P. Garnham, J.M. Peake, D. Cameron-Smith, Effect of exercise training on skeletal muscle cytokine expression in the elderly, Brain, behavior, and immunity 39 (2014) 80-86.
[36] J. Peake, K. Nosaka, M. Muthalib, K. Suzuki, Systemic inflammatory responses to maximal versus submaximal lengthening contractions of the elbow flexors, Exercise immunology review 12 (2005) 72-85.
[37] M.W. Feinberg, M.K. Jain, F. Werner, N.E. Sibinga, P. Wiesel, H. Wang, J.N. Topper, M.A. Perrella, M.-E. Lee, Transforming growth factor-β1 inhibits cytokine-mediated induction of human metalloelastase in macrophages, Journal of Biological Chemistry 275(33) (2000) 25766-25773.
[38] K.A. Volaklis, I. Smilios, A.T. Spassis, C.E. Zois, H.T. Douda, M. Halle, S.P. Tokmakidis, Acute pro-and anti-inflammatory responses to resistance exercise in patients with coronary artery disease: a pilot study, Journal of sports science & medicine 14(1) (2015) 91-97.
[39] S. Hering, C. Jost, H. Schulz, B. Hellmich, H. Schatz, A. Pfeiffer, Circulating transforming growth factor β1 (TGFβ1) is elevated by extensive exercise, European journal of applied physiology 86(5) (2002) 406-410.
[40] A.-M. Touvra, K.A. Volaklis, A.T. Spassis, C.E. Zois, H. Douda, K. Kotsa, S.P. Tokmakidis, Combined strength and aerobic training increases transforming growth factor-beta1 in patients with type 2 diabetes, Hormones (Athens) 10(2) (2011) 125-30.
[41] P. Gordon, E. Vannier, K. Hamada, J. Layne, B. Hurley, R. Roubenoff, C. Castaneda-Sceppa, Resistance training alters cytokine gene expression in skeletal muscle of adults with type 2 diabetes, International journal of immunopathology and pharmacology 19(4) (2006) 739-749.
[42] I. Bautmans, R. Njemini, S. Vasseur, H. Chabert, L. Moens, C. Demanet, T. Mets, Biochemical changes in response to intensive resistance exercise training in the elderly, Gerontology 51(4) (2005) 253-265.
[43] B. Schober-Halper, M. Hofmann, S. Oesen, B. Franzke, T. Wolf, E.-M. Strasser, N. Bachl, M. Quittan, K.-H. Wagner, B. Wessner, Elastic band resistance training influences transforming growth factor-ß receptor I mRNA expression in peripheral mononuclear cells of institutionalised older adults: the Vienna Active Ageing Study (VAAS), Immunity & Ageing 13(1) (2016) 22.
[44] D.J. Grainger, Transforming growth factor β and atherosclerosis: so far, so good for the protective cytokine hypothesis, Arteriosclerosis, thrombosis, and vascular biology 24(3) (2004) 399-404.