[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Indexing Sources::
Editorial Board::
Executive Members::
Articles Archive::
Instruction to Authors::
Peer-Review::
Contact Us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
:: Volume 23, Issue 4 (12-2021) ::
J Gorgan Univ Med Sci 2021, 23(4): 1-9 Back to browse issues page
Effect of Interval Exercise on Serum Level of Fibroblast Growth Factor 21 and Myostatin in Obese and Overweight Males: A Clinical Trial Study
Saeed Ramezani 1, Ali Asghar Ravasi2 , Siroos Choobineh3 , Zeynab Firozeh4
1- Ph.D in Exercise Physiology, Bojnourd Education Department, Bojnourd, Iran. , rsaeid92@gmail.com
2- Professor of Exercise Physiology, Department of Physical Education, University of Tehran, Tehran, Iran.
3- Associate Professor of Exercise Physiology, Department of Physical Education, University of Tehran, Tehran, Iran.
4- Ph.D in Exercise Physiology, Bojnourd Education Department, Bojnourd, Iran.
Abstract:   (3643 Views)
Background and Objective: Differentiation of white adipose tissue into brown through hormonal and non-hormonal factors, causes weight loss and weakens in obese and overweight people. This study was performed to determine the effect of 12 weeks of interval exercise with different intensities on serum levels of fibroblast growth factor 21 and myostatin in obese and overweight males.
Methods: This clinical trial study was done on 47 obese and overweight males (20.5±0.73 years old). Subjects were randomly divided into four groups: control, interval exercise with low intensity, moderate intensity and high intensity. The exercise program consisted of 12weeks of interval exercise with light, medium and heavy intensity respectively with 58-63, 73-78 and 88-93 percent of Reserve heart rate for 25 to 63 minutes and three sessions per week. Serum indices of fibroblast growth factor 21 and myostatin were measured using fasting blood sample 48 hours before and after exercise program using ELISA method.
Results: Performing 12 weeks of interval training with different intensities was not contribute to significant changes in the serum levels of fibroblast growth factor 21 and myostatin. Implementation of interval exercise at moderate and high intensities was associated with reduction of body fat percentage and increasing in maximal oxygen consumption (VO2max) in overweight and obese men (P<0.05).
Conclusion: Performing 12 weeks of low, medium and high intensity interval training without changing the serum level of fibroblast growth factor 21 and myostatin has a beneficial effect on improving body composition and increasing VO2max in obese and overweight young males.
Keywords: Interval Exercise , Obesity [MeSH], Myostatin [MeSH], Fibroblast Growth Factor 21 [MeSH]
Article ID: Vol23-47
Full-Text [PDF 719 kb]   (13766 Downloads)    
Type of Study: Original Articles | Subject: Exercise Physiology
References
1. Rolfe DF, Brown GC. Cellular energy utilization and molecular origin of standard metabolic rate in mammals. Physiol Rev. 1997 Jul; 77(3): 731-58. DOI: 10.1152/physrev.1997.77.3.731 [DOI] [PubMed]
2. Kajimura S, Saito M. A new era in brown adipose tissue biology: molecular control of brown fat development and energy homeostasis. Annu Rev Physiol. 2014; 76: 225-49. DOI: 10.1146/annurev-physiol-021113-170252 [DOI] [PubMed]
3. Zhang Y, Wang D, LiuY, Zhang Y, Liu Y, SuZ, Luo T. Impacts of chronic exercise on human blood fibroblast growth factor 21 levels in normal people: a meta-analysis. Biomedical Research. 2017; 28(13): 5726-32. [View at Publisher]
4. Park JG, Xu X, Cho S, Hur KY, Lee MS, Kersten S, Lee AH. CREBH-FGF21 axis improves hepatic steatosis by suppressing adipose tissue lipolysis. Sci Rep. 2016 Jun; 6: 27938. DOI: 10.1038/srep27938 [DOI] [PubMed]
5. Zhang X, Yeung DCY, Karpisek M, Stejskal D, Zhou ZG, Liu F, et al. Serum FGF21 levels are increased in obesity and are independently associated with the metabolic syndrome in humans. Diabetes. 2008 May; 57(5): 1246-53. DOI: 10.2337/db07-1476 [DOI] [PubMed]
6. Sargeant JA, Aithal GP, Takamura T, Misu H, Takayama H, Douglas JA, et al. The influence of adiposity and acute exercise on circulating hepatokines in normal-weight and overweight/obese men. Appl Physiol Nutr Metab. 2018 May; 43(5): 482-90. DOI: 10.1139/apnm-2017-0639 [DOI] [PubMed]
7. Willis SA, Sargeant JA, Thackray AE, Yates T, Stensel DJ, Aithal GP, et al. Effect of exercise intensity on circulating hepatokine concentrations in healthy men. Appl Physiol Nutr Metab. 2019 Oct; 44(10): 1065-72. DOI: 10.1139/apnm-2018-0818 [DOI] [PubMed]
8. Segsworth BM. Acute sprint interval exercise induces a greater FGF-21 response in comparison to work-matched continuous exercise. Electronic Thesis and Dissertation Repository. 2015. [View at Publisher]
9. Besse-Patin A, Montastier E, Vinel C, Castan-Laurell I, Louche K, Dray C, et al. Effect of endurance training on skeletal muscle myokine expression in obese men: identification of apelin as a novel myokine. Int J Obes (Lond). 2014 May; 38(5): 707-13. DOI: 10.1038/ijo.2013.158 [DOI] [PubMed]
10. Scalzo RL, Peltonen GL, Giordano GR, Binns SE, Klochak AL, Paris HLR, et al. Regulators of human white adipose browning: evidence for sympathetic control and sexual dimorphic responses to sprint interval training. PLoS One. 2014 Mar; 9(6): e90696. DOI: 10.1371/journal.pone.0090696 [DOI] [PubMed]
11. Feldman BJ, Streeper RS, Farese Jr RV, Yamamoto KR. Myostatin modulates adipogenesis to generate adipocytes with favorable metabolic effects. Proc Natl Acad Sci U S A. 2006 Oct; 103(42): 15675-80. DOI: 10.1073/pnas.0607501103 [DOI] [PubMed]
12. Singh R, Braga M, Pervin S. Regulation of brown adipocyte metabolism by myostatin/follistatin signaling. Front Cell Dev Biol. 2014 Oct; 2: 60. DOI: 10.3389/fcell.2014.00060 [DOI] [PubMed]
13. Ge X, Sathiakumar D, Lua BJG, Kukreti H, Lee M, McFarlane C. Myostatin signals through miR-34a to regulate Fndc5 expression and browning of white adipocytes. Int J Obes (Lond). 2017 Jan; 41(1): 137-48. DOI: 10.1038/ijo.2016.110 [DOI] [PubMed]
14. Hittel DS, Axelson M, Sarna N, Shearer J, Huffman KM, Kraus WE. Myostatin decreases with aerobic exercise and associates with insulin resistance. Med Sci Sports Exerc. 2010 Nov; 42(11): 2023-9. DOI: 10.1249/MSS.0b013e3181e0b9a8 [DOI] [PubMed]
15. Bagheri R, Hooshmand Moghadam B, Church DD, Tinsley GM, Eskandari M, Hooshmand Moghadam B, et al. The effects of concurrent training order on body composition and serum concentrations of follistatin, myostatin and GDF11 in sarcopenic elderly men. Experimental Gerontology. 2020; 133: 110869. DOI: 10.1016/j.exger.2020.110869 [Article] [DOI]
16. Kabak B, Belviranli M, Okudan N. Irisin and myostatin responses to acute high-intensity interval exercise in humans. Horm Mol Biol Clin Investig. 2018 Mar; 35(3): /j/hmbci.2018.35.issue-3/hmbci-2018-0008/hmbci-2018-0008.xml. DOI: 10.1515/hmbci-2018-0008 [DOI] [PubMed]
17. Jackson AS, Pollock ML. Generalized equations for predicting body density of men. Br J Nutr. 1978 Nov; 40(3): 497-504. DOI: 10.1079/bjn19780152 [DOI] [PubMed]
18. Kline GM, Porcari JP, Hintermeister R, Freedson PS, Ward A, McCarron RF, et al. Estimation of VO2max from a one-mile track walk, gender, age, and body weight. Med Sci Sports Exerc. 1987 Jun; 19(3): 253-59. [PubMed]
19. American College of Sports Medicine. ACSM's Guidelines for Exercise Testing and Prescription. 8th ed. Philadelphia: Lippincott Williams & Wilkins. 2009.
20. Margaria P, Cerretelli P, Aghemo P, Sassi G. Energy cost of running. J Appl Physiol. 1963 Mar; 18: 367-70. DOI: 10.1152/jappl.1963.18.2.367 [DOI] [PubMed]
21. Uth N, Sørensen H, Overgaard K, Pedersen PK. Estimation of VO2max from the ratio between HRmax and HRrest--the Heart Rate Ratio Method. Eur J Appl Physiol. 2004 Jan; 91(1): 111-15. DOI: 10.1007/s00421-003-0988-y [DOI] [PubMed]
22. Tanaka H, Monahan KD, Seals DR. Age-predicted maximal heart rate revisited. J Am Coll Cardiol. 2001 Jan; 37(1): 153-56. DOI: 10.1016/s0735-1097(00)01054-8 [DOI] [PubMed]
23. Pugh LG. The influence of wind resistance in running and walking and the mechanical efficiency of work against horizontal or vertical forces. J Physiol. 1971 Mar; 213(2): 255-76. DOI: 10.1113/jphysiol.1971.sp009381 [DOI] [PubMed]
24. Cheragh Birjandi S, Saghebjoo M, Hedayati M. [Effect of high intensity interval training and L-Arginine supplementation on serum levels of fibroblast growth factor 21 and atrial natriuretic peptide in overweight and obese young men]. J Birjand Univ Med Sci. 2016; 23(3): 211-21. [Article in Persian] [View at Publisher]
25. Kong Z, Sun S, Liu M, Shi Q. Short-Term High-Intensity Interval Training on Body Composition and Blood Glucose in Overweight and Obese Young Women. J Diabetes Res. 2016; 2016: 4073618. DOI: 10.1155/2016/4073618 [DOI] [PubMed]
26. Cuevas-Ramos D, Almeda-Valdés P, Meza-Arana CE, Brito-Córdova G, Gómez-Pérez FJ, Mehta R, et al. Exercise increases serum fibroblast growth factor 21 (FGF21) levels. PLoS One. 2012; 7(5): e38022. DOI: 10.1371/journal.pone.0038022 [DOI] [PubMed]
27. Taniguchi H, Tanisawa K, Sun X, Kubo T, Higuchi M. Endurance Exercise Reduces Hepatic Fat Content and Serum Fibroblast Growth Factor 21 Levels in Elderly Men. J Clin Endocrinol Metab. 2016 Jan; 101(1): 191-98. DOI: 10.1210/jc.2015-3308 [DOI] [PubMed]
28. Markan KR, Naber MC, Ameka MK, Anderegg MD, Mangelsdorf DJ, Kliewer SA, et al. Circulating FGF21 is liver derived and enhances glucose uptake during refeeding and overfeeding. Diabetes. 2014 Dec; 63(12): 4057-63. DOI: 10.2337/db14-0595 [DOI] [PubMed]
29. Fisher FM, Kleiner S, Douris N, Fox EC, Mepani RJ, Verdeguer F, et al. FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis. Genes Dev. 2012 Feb; 26(3): 271-81. DOI: 10.1101/gad.177857.111 [DOI] [PubMed]
30. Fletcher JA, Linden MA, Sheldon RD, Meers GM, Morris EM, Butterfield A, et al. Fibroblast growth factor 21 and exercise-induced hepatic mitochondrial adaptations. Am J Physiol Gastrointest Liver Physiol. 2016 May; 310(10): G832-43. DOI: 10.1152/ajpgi.00355.2015 [DOI] [PubMed]
31. Yie J, Hecht R, Patel J, Stevens J, Wang W, Hawkins N, et al. FGF21 N- and C-termini play different roles in receptor interaction and activation. FEBS Lett. 2009 Jan; 583(1): 19-24. DOI: 10.1016/j.febslet.2008.11.023 [DOI] [PubMed]
32. Estall JL, Ruas JL, Choi CS, Laznik D, Badman M, Maratos-Flier E, et al. PGC-1alpha negatively regulates hepatic FGF21 expression by modulating the heme/Rev-Erb(alpha) axis. Proc Natl Acad Sci U S A. 2009 Dec; 106(52): 22510-5. DOI: 10.1073/pnas.0912533106 [DOI] [PubMed]
33. Elliott BT, Herbert P, Sculthorpe N, Grace FM, Stratton D, Hayes LD. Lifelong exercise, but not short-term high-intensity interval training, increases GDF11, a marker of successful aging: a preliminary investigation. Physiol Rep. 2017 Jul; 5(13): e13343. DOI: 10.14814/phy2.13343 [DOI] [PubMed]
34. Shabani R, Izaddoust F. Effects of aerobic training, resistance training, or both on circulating irisin and myostatin in untrained women. Acta Gymnica. 2018; 48(2): 47-55. DOI: 10.5507/ag.2018.007 [Article] [DOI]
35. Jensky NE, Sims JK, Dieli-Conwright CM, Sattler FR, Rice JC, Schroeder ET. Exercise does not influence myostatin and follistatin messenger RNA expression in young women. J Strength Cond Res. 2010 Feb; 24(2): 522-30. DOI: 10.1519/JSC.0b013e3181c8664f [DOI] [PubMed]
36. Fu T, Seok S, Choi S, Huang Z, Suino-Powell K, Xu HE, et al. MicroRNA 34a inhibits beige and brown fat formation in obesity in part by suppressing adipocyte fibroblast growth factor 21 signaling and SIRT1 function. Mol Cell Biol. 2014 Nov; 34(22): 4130-42. DOI: 10.1128/MCB.00596-14 [DOI] [PubMed]
37. Horowitz JF, Klein S. Lipid metabolism during endurance exercise. Am J Clin Nutr. 2000 Aug; 72(2 Suppl): 558S-63S. DOI: 10.1093/ajcn/72.2.558S [DOI] [PubMed]
38. Knuth CM, Peppler WT, Townsend LK, Miotto PM, Gudiksen A, Wright DC. Prior exercise training improves cold tolerance independent of indices associated with non-shivering thermogenesis. J Physiol. 2018 Sep; 596(18): 4375-91. DOI: 10.1113/JP276228 [DOI] [PubMed]
39. Dohlmann TL, Hindsø M, Dela F, Helge JW, Larsen S. High-intensity interval training changes mitochondrial respiratory capacity differently in adipose tissue and skeletal muscle. Physiol Rep. 2018 Sep; 6(18): e13857. DOI: 10.14814/phy2.13857 [DOI] [PubMed]
40. Cunha Brandao CF, de Carvalho FG, de Oliveira Souza A, Morandi Junqueira-Franco MV, Batitucci G, Couto-Lima CA, et al. Physical training, UCP1 expression, mitochondrial density, and coupling in adipose tissue from women with obesity. Scand J Med Sci Sports. 2019 Nov; 29(11): 1699-706. DOI: 10.1111/sms.13514 [DOI] [PubMed]
41. Tsiloulis T, Carey AL, Bayliss J, Canny B, Meex RCR, Watt MJ. No evidence of white adipocyte browning after endurance exercise training in obese men. Int J Obes (Lond). 2018 Apr; 42(4): 721-27. DOI: 10.1038/ijo.2017.295 [DOI] [PubMed]
Send email to the article author


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ramezani S, Ravasi A A, Choobineh S, Firozeh Z. Effect of Interval Exercise on Serum Level of Fibroblast Growth Factor 21 and Myostatin in Obese and Overweight Males: A Clinical Trial Study. J Gorgan Univ Med Sci 2021; 23 (4) :1-9
URL: http://goums.ac.ir/journal/article-1-3900-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 23, Issue 4 (12-2021) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
Persian site map - English site map - Created in 0.06 seconds with 36 queries by YEKTAWEB 4645