نوع مقاله : مقاله پژوهشی

نویسندگان

1 دکترای تخصصی فیزیولوژی ورزش، گروه تربیت بدنی، دانشگاه فرهنگیان، تهران، ایران.

2 دانشیار گروه فیزیولوژی ورزشی دانشکده تربیت بدنی و علوم ورزشی دانشگاه فردوسی مشهد، مشهد، ایران.

3 دکترای تخصصی فیزیولوژی ورزش، گروه تربیت بدنی، واحد نیشابور، دانشگاه آزاد اسلامی، نیشابور، ایران.

چکیده

زمینه وهدف: آیریزین که توسط عضله اسکلتی در پاسخ به فعالیت ورزشی تولید می‌شود، اخیراً به‌عنوان هدف درمانی برای بیماری‌های متابولیک گزارش شده است. هدف از پژوهش حاضر ‌بررسی تأثیر هشت هفته تمرین مقاومتی و استقامتی بر سطوح آیریزین بافت کبد و عضله دوقلو در موش‌های صحرایی نر است.
مواد و روش‌ها:در این پژوهش 15سر موش صحرایی نر به‌طور تصادفی به سه گروه کنترل(5 سر)،تمرین استقامتی(5 سر)و تمرین مقاومتی(5 سر)، تقسیم شدند.گروه استقامتی تمرینات را به مدت هشت هفته روی نوارگردان وگروه مقاومتی نیزتمرینات مقاومتی را به مدت هشت هفته روی نردبان یک متری با شیب 85 درجه انجام دادندو گروه کنترل در این مدت بدون تمرین بودند.72 ساعت پس از آخرین جلسه تمرین حیوانات بیهوش و بافت کبدو عضله دوقلو برداشته شد. از آزمون شاپیروویلک جهت تعیین توزیع طبیعی داده‌ها،و از آزمون‌آنالیز واریانس یک طرفه و آزمون تعقیبی توکی برای تجزیه و تحلیل داده‌ها استفاده گردیدو معنی‌داری در سطح 05/0 ≥P پذیرفته شد.
یافته‌ها:پس ازتأیید توزیع طبیعی داده‌ها با آزمون شاپیروویلک،نتایج آزمون آنالیز واریانس یک‌طرفه اختلاف معنی‌داری را در مقادیر آیریزین بافت کبد و عضله دوقلو در بین گروه‌ها نشان داد(به‌ترتیب؛ 001/0P=، 016/0=P).آزمون تعقیبی توکی نیز افزایش معنی‌داری را در مقادیر آیریزین عضله دوقلو در گروه تمرین استقامتی و تمرین مقاومتی نسبت به گروه کنترل نشان داد(به‌ترتیب؛016/0P=، 061/0=P).همچنین آزمون تعقیبی توکی نشان داد که افزایش معنی‌داری در مقادیر آیریزین بافت کبد در گروه تمرین استقامتی و تمرین مقاومتی نسبت به گروه کنترل وجود دارد(به‌ترتیب؛ 001/0P=، 001/0=P). اما اختلاف معنی‌داری در مقادیر آیریزین بافت کبدو عضله دوقلو بین گروه‌های تمرینی وجود نداشت(به‌ترتیب؛ 962/0P =، 742/0= P).
نتیجه‌گیری:براساس نتایج پژوهش حاضر، هر دو تمرینات مقاومتی و استقامتی می‌تواند سطوح آیریزین را در هر دو بافت کبدو عضله دوقلو به‌طور معنی‌داری افزایش دهد که به‌نظر می‌رسد فعالیت ورزشی از این طریق می‌تواند اثرات مفیدی در پیشگیری و درمان بیماری‌های متابولیک داشته‌باشد.

کلیدواژه‌ها

موضوعات

عنوان مقاله [English]

The Effect of Eight Weeks Progressive Resistance and Endurance Training on Liver Tissue and Gastrocnemius Muscle’s Irisin levels in Male Rats

نویسندگان [English]

  • Mohammad Hoseinzadeh 1
  • Amir Rashidlamir 2
  • farida sadeghi fazel 3
  • Rambod Khajei 3

1 PhD. in sport physiology, Department of physical education, Farhagian University, Tehran, Iran

2 Associate Professor, Department of physical education, Ferdowsi University of Mashhad, Mashhad,Iran.

3 PhD. in sport physiology, Department of physical education, Neyshabur branch, Islamic Azad University, Neyshabur, Iran.

چکیده [English]

Background and purpose:Irisin, which is released in response to physical activity, has recently been reported as the therapeutic target in metabolic disorders. The present study attempts to discover the effect of eight weeks’ resistance or endurance training on the irisin level in rats’ gastrocnemius and liver.

Materials and methods:To this purpose,15 male rats were randomly assigned to three groups of 5: the resistance group, the endurance group, and the control group. For 8 weeks, the resistance group did the activities on the treadmill and the endurance group on a one-meter-long ladder with 85 steep, while the control group did not receive any training. 72 hours after their last training session, the subjects were anaesthetized and their liver and gastrocnemius were removed. A Shapiro-Wilk test was run to determine the normal distribution of data, and a one-way ANOVA and a Tukey test were applied to analyze the data(P ≥ 0.05).
Results: The normal distribution having been approved via the Shapiro-Wilk test, the one-way ANOVA showed a significant difference in the irisin levels between the groups’ livers and gastrocnemii (P =0.001 and P -0.016, respectively). The Tukey test revealed a significant rise in the liver tissue of the resistance group and endurance group in comparison to the control group (P =0.001 and P =0.742, respectively).

Conclusion:According to this study, both resistance and endurance training can help significantly increase the irisin level of both the liver and the gastrocnemius, indicating how physical activity can help in the prevention and treatment of metabolic illnesses.

کلیدواژه‌ها [English]

  • Resistance training
  • Endurance Training
  • Irisin
  • Liver
  • Gastrocnemius Muscle
[1]. Huh JY, Siopi A, Mouqios V, Park KH, Mantzoros CS.Irisin in response to exercise in humans with and without
metabolic syndrome. J Clin Endocrinol Metab. 2015;100(3): 453-7.
[2]. EsfahaniM, BaranchiM, Goodarzi MT. Irisin and Metabol ic Disorders. Avicenna J Med Biochem. 2016;4(1): e33230.
[3]. Aydin S. Three new players in energy regulation: Preptin,adropinand irisin. Peptides. 2014; 56: 94-110.
[4]. Barja-Fernández S, Folgueira C, Castelao C, Al-Massadi O,Bravo SB, Garcia-Caballero T, et al. FNDC5 is produced in
the stomach and associated to body composition. Scientific Reports. 2016;6:23067.
[5]. Schumacher MA, Chinnam N, Ohashi T, Shah RS,Erickson HP. The Structure of Irisin Reveals a Novel Intersubunit-Sheet Fibronectin Type III (FNIII) Dimer.Journal of Biologycal Chemisty. 2013; 288(47):33738-44.
[6]. Askari H, Rajani SF, Poorebrahim M, Haghi-Aminjan H,Raeis-Abdollahi E, Abdollahi. A glance at the therapeutic otential of irisin against diseases involving inflammation, oxidative stress, and apoptosis: An introductory review. Pharmacological Research. 2018;129: 44–55.
[7]. Soliman NA, Asalah AK, Moursi SM, Gamal SM, Eldeen MA. Effect of Exercise Training on Metabolic Homeostasis
and Some Hemodynamics (Some Hepatic and Cardiovascular Functions) in Experimentally Induced Obesity. J Obes Weight Loss Ther. 2018; 8: 368.
[8]. Zhang Y, Li R, Meng Y, Li Sh, Donelan W, Zhao Y et al.Irisin Stimulates Browning of White Adipocytes Through
Mitogen-Activated Protein Kinase p38 MAP Kinase and ERK MAP Kinase Signaling. Diabetes, 2014; 83: 514-25.
[9]. Pedersen BK, Febbraio MA. Muscles, exercise and obesity:skeletal muscle as a secretory organ. Nat. Rev.Endocrinol. 2012; 8: 457–65.
[10]. Dewal RS, StanfordKI. Effects of exercise on brown and beige adipocytes. Biochim Biophys Acta. 2018; 1388-1981(18): 30075-1.
[11]. Arias-Loste MT, Ranchal I, Romero-Gómez M, Crespo J.Irisin, a Link among Fatty Liver Disease, Physical Inactivity and Insulin Resistance. Int. J. Mol. Sci. 2014; 15:23163-78.
[12]. Silva-Magosso NS, Barbosa MR, Tomaz LM, Rodrigues MFC, Magosso RF, Canevazzi GH, et al. Irisin Signaling
Pathway is up Regulated by Resistance Training in Ovariectomized Rats. Obes Control Ther. 2017; 4(2): 1-7.
[13]. Khodadadi H, Rajabi H, Seyyed Reza Attarzadeh S R,Abbasian S. The Effect of High Intensity Interval Training
(HIIT) and Pilates on Levels of Irisin and Insulin Resistance in Overweight Women. Iranian Journal of Endocrinology and Metabolism 2014; 16(3): 190-6.[persion]
[14]. Jones A, Carter H. The Effect of Endurance Training on Parameters of Aerobic Fitness. Sports Med 2000; 29 (6):
373-86.
[15]. Khalafi M, Shabkhiz F, Azali Alamdari K, Bakhtiyari A.Irisin Response to Two Types of Exercise Training in Type
2 Diabetic Male Rats. Arak Medical University Journal (AMUJ). 2016; 19(111): 37-45.[persion]
[16]. Mombini H, Eslami Farsani M, Ab Abzadeh S, Barzegar H,Vahdat H. Effect of High-Intensity Interval Training (HIIT)
on the Levels of Irisin and Interleukin-10 in Overweight Men. Qom Univ Med Sci. 2018; 12(2): 35-44. [persion]
[17]. Kim HJ, Lee HJ, SO B, Son JS, Yoon D, Song W. Effect of aerobic training and resistance training on circulating
irisin level and their association with change of body composition in overweight/obese adults: a pilot study.Physiological Research Praha. 2016; 65(2): 271-9.
[18]. Reisi J, Rajabi H, Ghaedi K, Marandi SM, Dehkhoda MR.Effect of Acute Resistance Training on Plasma Irisin Protein Level and Expression of Muscle FNDC5 and Adipose Tissue UCP1 Genes in Male Rats. J Isfahan Med Sch, 2013; 31(256): 1657-66.
[19]. Disanzo BL, You T. Effects of exercise training on indicators of adipose tissue angiogenesis and hypoxia in obese rats. Metabolism Clinical and Experimental. 2014;63(4):452-5.
[20]. Matinhomaee H, Ziaolhagh SJ, Azarbayjani MA, Piri M.Effects of Boldenone consumption and resistance exercise
on hepatocyte morphologic damages in male wistar rats.European Journal of Experimental Biology. 2014; 4(2): 211-4.
[21]. Reisi J, Rajabi H, Ghaedi K, Marandi SM, Asadysamani Z,Kazeminasab F. Effect of eight weeks’ resistance training
on plasma irisin protein level and muscle FNDC5 and adipose tissue UCP1 genes expression in male rats.Exercise phisiology. 2015; 7(28):117- 30.
[22]. Soori R, Ravasi AA, HazratiMolaee S. Comparing the Effects of High Intensity Endurance Training and Resistance Training on Irisin Levels and Insulin Resistance in Rats. Iranian Journal of Endocrinology and Metabolism.2015; 17(3):24-.
[23]. Bonfante I. L, Chacon-Mikahil M. P, Brunelli D. T, Gaspari A. F, Duft R. G, Lopes W. A, et. al. Combined training,
FNDC5/irisin levels and metabolic markers in obese men:A randomised controlledtrial. Eur J Sport Sci. 2017; 17(5):629-37.
[24]. Zhao J, Su Z, Qu C, DongY. Effects of 12 Weeks Resistance Training on Serum Irisin in Older Male Adults. Front
Physiol. 2017; 8: 171.
[25]. Pekkala S, Wiklund P. K, Hulmi J. J, Ahtiainen J. P,Horttanainen M, Pollanen E, et. al. Are skeletal muscle FNDC5 gene expression and irisin release regulated by exercise and related to health?.j Physiol.2013;591(21):5393-400.
[26]. Fain J. N, Company J. M, Booth F. W, Laughlin M. H, Padilla J, Jenkins N. T, et. al. Exercise training does not increase muscle FNDC5 protein or mRNA expression in pigs. Metabolism. 2013;62(10): 1503-11.
[27]. Xie Ch, Zhang Y, Tran T, Wang H, Li Sh, Vertes George, et al. Irisin Controls Growth, Intracellular Ca2+ signals,andMitochondrial Thermogenesis in Cardiomyoblasts.PLoS ONE, 2015; 10(8): e0136816.
[28]. Keating S.E, Hackett D.A, George J, Johnson N.A.Exerciseand non-alcoholic fatty liver disease: A systematic
review and meta-analysis. J. Hepatol. 2012; 57: 157–66.
[29]. Zhang H.J, Zhang X.F, Ma Z.M, Pan L.L, Chen Z, Han H.W, et al. Irisin is inversely associated with intrahepatic
triglyceride contents in obese adults. J. Hepatol. 2013; 59:557–62.
[30]. Polyzos SA, Kountouras J, Shields K, Mantzoros CS. Irisin:A renaissance in metabolism? Metabolism. 2013; 62: 1037–44.
[31]. Hondares E, Rosell M, Diaz-Delfin J, Olmos Y, Monsalve M, Iglesias R, et. al. Peroxisome proliferator-activated
receptor alpha (PPARalpha) induces PPARgamma coactivator 1alpha (PGC-1alpha) gene expression and contributes to thermogenic activation of brown fat:Involvement of PRDM16. J. Biol. Chem. 2011; 286: 43112–22.
[32]. Barbera M.J, Schluter A, Pedraza N, Iglesias R, Villarroya F, Giralt M. Peroxisome proliferator-activated receptor
alpha activates transcription of the brown fat uncoupling protein-1 gene. A link between regulation of the thermogenic and lipid oxidation pathways in the brown fat cell. J. Biol. Chem. 2001: 276: 1486–93.
[33]. Xu J, Lloyd D.J, Hale C, Stanislaus S, Chen M, Sivits G, et al. Fibroblast growth factor 21 reverses hepatic steatosis,
increases energy expenditure, and improves insulin sensitivity in diet-induced obese mice. Diabetes. 2009; 58:250–9.
[34]. Mo L, Shen J, Liu Q, Zhang Y, Kuang J, Pu SH et al. IrisinIs Regulated by CAR in Liver and Is a Mediator of Hepatic
Glucose and Lipid Metabolism. Mol Endocrinol. 2016.
[35]. Tang h, Yu R, Liu Sh, Huwatibieke B, Li Z, Zhang W. IrisinInhibits Hepatic Cholesterol Synthesis via AMPK-SREBP2
Signaling. EbioMedicine. 2016.
[36]. American College of Sports Medicine position stand: therecommended quantity and quality of exercise for
developing and maintaining cardio-respiratory andmuscular fitness in healthy adults.Med Sci Sports Exerc.1990;22:265–274.
[37]. Reisi J, Ghaedi K, Rajabi H, Marandi SM. Can ResistanceExercise Alter Irisin Levels and Expression Profiles of
FNDC5 and UCP1 inRats?. Asian J SportsMed. 2016; 7(4):e35205.
[38]. Roca-Rivada A, Castelao C, L. Senin l, O. Landrove M,Baltar j, Crujeiras A B et al. FNDC5/Irisin Is Not Only a
Myokine but Also an Adipokine. PLOS ONE. 2013; 8(4): 1-10.
[39]. Huh JY, Panagiotou G, Mougios V, et al. FNDC5 and irisininhumans: I Predictors of circulating concentrations in
serumand plasma and II. mRNA expression andcirculatingconcentrations in response to weight loss and exercise.Metabolism 2012;61(12):1725–38.
[40]. Moon HS, Dincer F, Mantzoros CS. Pharmacologicalconcen-trations of irisin increase cell proliferation without influenc-ing markers of neurite outgrowth andsynaptogenesis inmouse H19-7 hippocampal cell lines.Metabolism. 2013; 62(8): 1131–6.