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

نویسندگان

1 استادیار گروه تربیت بدنی، واحد نیشابور، دانشگاه ازاد اسلامی، نیشابور، ایران،

2 استاد گروه فیزیولوژی ورزشی، دانشگاه ازاد اسلامی، واحد تهران مرکزی، تهران، ایران،

3 دانشیار گروه فیزیولوژی ورزشی، دانشگاه ازاد اسلامی، واحد تهران مرکزی، تهران، ایران،

4 کارشناسی ارشد، مربی، آموزش و پرورش ناحیه ٥ مشهد، خراسان رضوی، ایران،

5 دکتری فیزیولوژی ورزش، مربی، اموزش و پرورش ناحیه ١ مشهد، خراسان رضوی، ایران

چکیده

هدف: با این که چاقی در تمام دنیا فراگیر شده است تلاش برای کاهش این اپیدمیک موثر نبوده است. بنابراین نیاز به یافتن راه های جدید پیشگیری از چاقی وجود دارد. هدف از انجام این پژوهش تعیین اثر تمرین استقامتی و آدنوزین بر بیان ژن A1AR در بافت  چربی احشایی رت های نر چاق  بود.
روش‌شناسی: بیست سر رت نر صحرایی، نژاد ویستار به مدت دوازده هفته با غذای پر چرب تغذیه شدند تا به میانگین وزنی 30±319 گرم رسیدند. پس از همسان سازی، رت ها به صورت تصادفی در چهار گروه کنترل-سالین، کنترل-آدنوزین، تمرین-آدنوزین و تمرین-سالین تقسیم شدند. برنامه تمرینی شامل دویدن روی نوارگردان بدون شیب به مدت 12 هفته بود. هر هفته پنج جلسه با سرعت 25-20متر در دقیقه و به مدت31-15 دقیقه اجرا شد. برای اندازه‌گیری  بیان نسبی ژن A1AR از روش PCR  استفاده شد. اطلاعات جمع آوری شده با استفاده از روش آماری آنالیز واریانس دو طرفه مورد بررسی قرار گرفت.
یافته‌ها: هر دو متغیر تمرین استقامتی و مصرف آدنوزین (به‌طور مستقل) کاهش معنی داری را در تغییرات بیان ژن A1AR بافت چربی احشایی نشان دادند (001/0= P). همچنین اثرات تعاملی تمرین و آدنوزین حاکی از کاهش معنی‌دار در تغییرات بیان نسبی ژن A1AR بود (003/0=P)
نتیجه‌گیری: تمرینات استقامتی و مصرف آدنوزین به عنوان آنتاگونیست های A1AR ، محرک‌های قوی لیپولیز بافت چربی هستند و این پتانسیل را دارند که به عنوان عوامل لیپولیتیک موثر در چاقی به کار گرفته شوند.
 

کلیدواژه‌ها

عنوان مقاله [English]

The effect of endurance training and adenosine consumption on the a1ar gene expression in the visceral adipose tissue of obese male rats

نویسندگان [English]

  • A Barjaste Yazdi 1
  • MA Azarbayjani 2
  • H Matin Homaee 3
  • M Peeri 2
  • F Torabi 4
  • Z Ramezani 5

1 Assistant Professor, Department of Exercise Physiology, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran

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

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

4 Master's in Physical Education, Instructor, Department of Education, District 5, Mashhad, Khorassan-e-Razavi, Iran

5 PhD in Sport Physiology, Instructor, Department of Education, District 1, Mashhad, Khorassan-e-Razavi, Iran

چکیده [English]

Aim: Although obesity is becoming epidemic all around the world, the effort to reduce its prevalence has not been effective. Thus, there is a need to find further paths to prevent obesity. The aim of this study was to determine the effect of endurance training and adenosine on the A1AR gene expression in the visceral adipose tissue of obese male rats
Method: Twenty wistar strain male rats were fed with high-fat food for twelve weeks and reached the average weight of 319+-30 grams. The rats were divided randomly into four groups after being conformed. The exercise training session included running on the treadmill with no slope for 12 week. Each week, five sessions were held for 15-31 minutes with the speed of 20-25 meters per minute. In order to measure the relative gene expression of A1AR, the PCR method was used. The data was analyzed using the statistical method of two-way analysis of variance.
Results: both variable of endurance training and adenosine consumption (independently) demonstrated a significant decrease in the A1AR gene expression in the visceral adipose tissue. (P=0.001). Also, the intraction of training and adenosine affects significant reduction of the A1AR expression.
Conclusion: Endurance training and adenosine are strong stimulants of adipose tissue lipolysis as A1AR antagonists and have the potential to be used as effective lipolysis agents in obesity
Keywords: Endurance Training, A1AR, Visceral White Adipose Tissue.

کلیدواژه‌ها [English]

  • Keywords: Endurance Training
  • A1AR
  • Visceral White Adipose Tissue
  1. Bartelt A & Heeren J. (2014). Adipose tissue browning and metabolic health. Nature Reviews. Endocrinology 10 24–36.
  2. Harms M, Seale P. (2013). Brown and beige fat: development, function and therapeutic potential. Nat Med;19:1252-63.
  3. Dodd GT, Decherf S, Loh K, Simonds SE, Wiede F, Balland E, Merry TL, Munzberg H, Zhang ZY, Kahn BB et al. (2015). Leptin and insulin act on POMC neurons to promote the browning of white fat. Cell 160 88–104.
  4. Ruan HB, Dietrich MO, Liu ZW, Zimmer MR, Li MD, Singh JP, Zhang K, Yin R, Wu J, Horvath TL et al. (2014). O-GlcNAc transferase enables AgRP neurons to suppress browning of white fat. Cell 159 306–317.
  5. Daneshyar S, Kordi M, Gaeini A, Kadivar M, Afshari S.(2015). The effect of endurance training on gene expression of uncoupling protein 1(UCP-1) in white visceral adipose tissue of retroperitoneal depot of male Wistar rats. Razi Journal of Medical Sciences; Vol. 22, No.136.
  6. Rachid TL, Penna-de-Carvalho A, Bringhenti I, Aguila MB, Mandarim-de- Lacerda CA & Souza-Mello V.(2015). Fenofibrate (PPARa agonist) induces beige cell formation in subcutaneous white adipose tissue from diet-induced male obese mice. Molecular and Cellular Endocrinology 402 86–94. (doi:10.1016/j.mce.2014.12.027).
  7. Petrovic N, Walden TB, Shabalina IG, Timmons JA, Cannon B & Nedergaard J.(2010).Chronic peroxisome proliferator-activated receptor gamma (PPARgamma) activation of epididymally derived white adipocyte cultures reveals a population of thermogenically competent, UCP1-containing adipocytes molecularly distinct from classic brown adipocytes. Journal of Biological Chemistry 285 7153–7164.
  8. Coskun T, Bina HA, Schneider MA, Dunbar JD, Hu CC, Chen Y, Moller DE & Kharitonenkov A.(2008). Fibroblast growth factor 21 corrects obesity in mice. Endocrinology 149 6018–6027.
  9. Petruzzelli M, Schweiger M, Schreiber R, Campos-Olivas R, Tsoli M, Allen J, Swarbrick M, Rose-John S, Rincon M, Robertson G et al. (2014). A switch from white to brown fat increases energy expenditure in cancerassociated cachexia. Cell Metabolism 20 433–447.
  10. Bordicchia M, Liu D, Amri EZ, Ailhaud G, Dessi-Fulgheri P, Zhang C, Takahashi N, Sarzani R & Collins S.(2012). Cardiac natriuretic peptides act via p38 MAPK to induce the brown fat thermogenic program in mouse and human adipocytes. Journal of Clinical Investigation 122 1022–1036
  11. Gnad T, Scheibler S, von Kugelgen I, Scheele C, Kilic A, Glode A, Hoffmann LS, Reverte-Salisa L, Horn P, Mutlu S et al. (2014). Adenosine activates brown adipose tissue and recruits beige adipocytes via A2A receptors. Nature 516 395–399.
  12. Jimenez-Aranda A, Fernandez-Vazquez G, Campos D, Tassi M, Velasco-Perez L, Tan DX, Reiter RJ & Agil A.(2013). Melatonin induces browning of inguinal white adipose tissue in Zucker diabetic fatty rats. Journal of Pineal Research 55 416–423.
  13. Villanueva CJ, Vergnes L, Wang J, Drew BG, Hong C, Tu Y, Hu Y, Peng X, Xu F, Saez E et al. (2013). Adipose subtype-selective recruitment of TLE3 or Prdm16 by PPARgamma specifies lipid storage versus thermogenic gene programs. Cell Metabolism 17 423–435.
  14. Hoffmann LS, Etzrodt J, Willkomm L, Sanyal A, Scheja L, Fischer AW, Stasch JP, Bloch W, Friebe A, Heeren J et al. (2015). Stimulation of soluble guanylyl cyclase protects against obesity by recruiting brown adipose tissue. Nature Communications 6 7235.
  15. Hu F, Wang M, Xiao T, Yin B, He L, MengW, Dong M & Liu F.(2015). miR-30 promotes thermogenesis and the development of beige fat by targeting RIP140. Diabetes 64 2056–2068.
  16. Koupenova  M, Ravid K.(2014).Adenosine, Adenosine Receptors and Their Role in GlucoseHomeostasis and Lipid Metabolism. J Cell Physiol. Author manuscript; available in PMC 2014 September 04.
  17. Fain JN, Pointer RH, Ward WF .(1972). Effects of adenosine nucleosides on adenylate cyclase, phosphodiesterase, cyclic adenosine monophosphate accumulation, and lipolysis in fat cells. J Biol Chem 247:6866–6872.
  18. Ringholm S, Grunnet Knudsen J, Leick L, Lundgaard A, Munk Nielsen M, et al. (2013). PGC-1a Is Required for Exercise- and Exercise Training-Induced UCP1 Up-Regulation in Mouse White Adipose Tissue. PLoS ONE 8(5): e64123.
  19. Xu X, Ying Z, Cai M, Xu Z, Li Y, Jiang SY, et al.(2011). Exercise ameliorates high-fat diet-induced metabolic and vascular dysfunction, and increases adipocyte progenitor cell population in brown adipose tissue. Am J Physiol Regul Integr Comp Physiol;300(5):1115-25.
  20. Vannucci SJ, Klim CM, Martin LF, LaNoue KF. (1989). A1-adenosine receptor-mediated inhibition of adipocyte adenylate cyclase and lipolysis in Zucker rats. Am J Physiol 257: E871-E878.
  21. Kaartinen JM, LaNoue KF, Ohisalo JJ .(1994).Quantitation of inhibitory G-proteins in fat cells of obese and normal-weight human subjects. Biochim Biophys Acta;1201:69–75.
  22. Arvinder K, Dhalla, Jeffrey W Chisholm, Gerald M, Reaven, and Luiz Belardinelli.(2009). A1 Adenosine Receptor: Role in Diabetes and Obesity. Article in Handbook of experimental pharmacology · DOI: 10.1007/978-3-540-89615-9_9.
  23. Rosen, E D & Spiegelman B M.(2014). What we talk about when we talk about fat. Cell 156, 20–44.
  24. Nedergaard J, Cannon B.(2014). The browning of white adipose tissue: some burning issues. Cell Metab;20:396–407.
  25. Cao L, Choi EY, Liu X, Martin A, Wang C, Xu X, During MJ.(2011). White to brown fat phenotypic switch induced by genetic and environmental activation of a hypothalamic-adipocyte axis. Cell Metab;14:324-38.
  26. Pedersen BK, Febbraio MA.(2012). Muscles, exercise and obesity: skeletal muscle as a secretory organ. Nat Rev Endocrinol ;8:457–465.
  27. Bostrom P, Wu J, Jedrychowski MP, Korde A, Ye L, Lo JC, et al.(2012). A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature;481(7382):463-8.
  28. Rao RR, Long JZ, White JP, Svensson KJ, Lou J, Lokurkar I, JedrychowskiMP, Ruas JL, Wrann CD, Lo JC et al. (2014). Meteorin-like is a hormone that regulates immune-adipose interactions to increase beige fat thermogenesis. Cell 157 1279–1291.
  29. Feldman BJ, Streeper RS, Farese RV Jr, Yamamoto KR.(2006). Myostatin modulates adipogenesis to generate adipocytes with favorable metabolic effects. Proc Natl Acad Sci U S A;103:15675–15680.
  30. Roberts LD, Boström P, O’Sullivan JF, et al.(2014). b-Aminoisobutyric acid induces browning of white fat and hepatic b-oxidation and is inversely correlated with cardiometabolic risk factors. Cell Metab;19:96–108.