[صفحه اصلی ]   [Archive] [ English ]  
:: صفحه اصلي :: درباره مجله :: شماره جاری :: تمام شماره‌ها :: جستجو :: ثبت نام :: ارسال مقاله :: تماس با ما ::
بخش‌های اصلی
صفحه اصلی::
اطلاعات نشریه::
بانک‌ها و نمایه‌ها::
آرشیو مجله و مقالات::
برای نویسندگان::
اخلاق در پژوهش::
برای داوران::
تسهیلات پایگاه::
تماس با ما::
هوش مصنوعی::
::
Basic and Clinical Biochemistry and Nutrition
..
DOAJ
..
CINAHL
..
EBSCO
..
IMEMR
..
ISC
..
جستجو در پایگاه

جستجوی پیشرفته
..
دریافت اطلاعات پایگاه
نشانی پست الکترونیک خود را برای دریافت اطلاعات و اخبار پایگاه، در کادر زیر وارد کنید.
..
enamad
..
:: دوره 27، شماره 5 - ( دوماه نامه 1402 ) ::
جلد 27 شماره 5 صفحات 492-481 برگشت به فهرست نسخه ها
اثرات تمرین مقاومتی، تستوسترون و عصاره گرده نخل (Phoenix dactylifera L.) بر بیان ژن‌های FNDC5 و IGF1 بافت چربی قهوه‌ای در موش‌های صحرایی نر
علی اربطی ، حسن متین همایی* ، محمدعلی آذربایجانی ، صالح رحمتی
گروه فیزیولوژی ورزشی، واحد تهران مرکزی، دانشگاه آزاد اسلامی، تهران، ایران ، matinhomaeehasan@gmail.com
چکیده:   (991 مشاهده)
زمینه و هدف: استفاده از تستوسترون انانتات در بین ورزشکاران، به‌ویژه رشته ­های مقاومتی رواج دارد. با توجه به عوارض جانبی استفاده از تستوسترون انانتات، یافتن روش‌های جایگزین ضروری به نظر می‌رسد. مطالعه حاضر به مقایسه اثرات مستقل و تعاملی تمرین مقاومتی، تستوسترون و عصاره گرده نخل بر بیان ژن‌های FNDC5 و IGF1 بافت چربی قهوه‌ای در موش‌های صحرایی نر پرداخته است.
روش‌ها: در این مطالعه تجربی 36 سر موش صحرایی نر به طور تصادفی به 6 گروه‌ کنترل، تمرین مقاومتی، عصاره گرده نخل، تستوسترون انانتات، عصاره گرده نخل+تمرین مقاومتی و تستوسترون انانتات+تمرین مقاومتی تقسیم شدند. برنامه تمرین مقاومتی به مدت 4 هفته (5 روز در هفته) اجرا شد. در روزهای تمرین، گاواژ عصاره گرده نخل (100 میلی‌گرم/کیلوگرم) و تزریق تستوسترون (2 میلی‌گرم/کیلوگرم) در گروه‌های مربوطه انجام شد. 48 ساعت پس از آخرین مداخله، موش‌ها قربانی شدند، بافت چربی قهوه‌ای جمع‌آوری و به آزمایشگاه ارسال شد و بیان ژن های FNDC5 و IGF1 با Real-time PCR سنجش شد.
یافته‌ها: در رت­ ها تمرین مقاومتی موجب افزایش بیان ژن‌های FNDC5 و IGF1 بافت چربی قهوه‌ای شد (0/001=P). تستوسترون نیز موجب افزایش بیان ژن FNDC5 بافت چربی قهوه‌ای شد (0/013= P). اما عصاره گرده نخل تاثیر معنی ­داری بر بیان ژن‌های FNDC5 و IGF1 بافت چربی قهوه‌ای نداشت. همچنین اثر هم‌افزایی (سینرژیکی) معنی‌داری بین متغیرهای پژوهش یافت نشد (0/05>P).

نتیجه‌گیری: بر اساس نتایج حاضر، هر دو تمرین مقاومتی و تستوسترون به طور معنی داری باعث افزایش بیان ژن FNDC5 در بافت چربی قهوه‌ای در رتها شد اما بر IGF1 تاثیر معنی داری نداشت. عصاره گرده نخل نیز تاثیر معنی­داری بر بیان ژن‌های FNDC5 و IGF1 بافت چربی قهوه‌ای در رت­ها نداشت.
واژه‌های کلیدی: تمرین مقاومتی، بافت چربی قهوه‌ای، تستوسترون، عصاره گرده نخل، بیان ژن
متن کامل [PDF 542 kb]   (693 دریافت)    
نوع مطالعه: پژوهشي | موضوع مقاله: عمومى
دریافت: 1401/9/10 | ویرایش نهایی: 1402/9/19 | پذیرش: 1402/7/25 | انتشار: 1402/5/10
فهرست منابع
1. Al-Zoubi RM, Yassin AA, Alwani M, Al-Qudimat A, Aboumarzouk OM, Zarour A, Al Ansari A. A systematic review on the latest developments in testosterone therapy: Innovations, advances, and paradigm shifts. Arab journal of urology. 2021; 19(3): 370-5. doi: 10.1080/2090598x.2021.1959260.
2. Pastuszak AW, Gomez LP, Scovell JM, Khera M, Lamb DJ, Lipshultz LI. Comparison of the Effects of Testosterone Gels, Injections, and Pellets on Serum Hormones, Erythrocytosis, Lipids, and Prostate-Specific Antigen. Sexual medicine. 2015; 3(3):165-73. doi: 10.1002/sm2.76.
3. Falqueto H, Dos Santos MR, Manfredi LH. Anabolic-Androgenic Steroids and Exercise Training: Breaking the Myths and Dealing With Better Outcome in Sarcopenia. Frontiers in physiology. 2022;13:838526. doi: 10.3389/fphys.2022.838526.
4. Vingren JL, Kraemer WJ, Ratamess NA, Anderson JM, Volek JS, Maresh CM. Testosterone physiology in resistance exercise and training: the up-stream regulatory elements. Sports medicine (Auckland, NZ). 2010;40(12):1037-53. doi: 10.2165/11536910-000000000-00000.
5. Bachman E, Travison TG, Basaria S, Davda MN, Guo W, Li M, et al. Testosterone induces erythrocytosis via increased erythropoietin and suppressed hepcidin: evidence for a new erythropoietin/hemoglobin set point. The journals of gerontology Series A, Biological sciences and medical sciences. 2014;69(6):725-35. doi: 10.1093/gerona/glt154.
6. de Almeida Ferreira M, Mendonça JA. Long-term testosterone replacement therapy reduces fatigue in men with hypogonadism. Drugs in context. 2022;11. doi: 10.7573/dic.2021-8-12.
7. Kelly DM, Jones TH. Testosterone: a metabolic hormone in health and disease. J Endocrinol. 2013; 217(3): R25-45. doi: 10.1530/JOE-12-0455.
8. Kelly DM, Akhtar S, Sellers DJ, Muraleedharan V, Channer KS, Jones TH. Testosterone differentially regulates targets of lipid and glucose metabolism in liver, muscle and adipose tissues of the testicular feminised mouse. Endocrine. 2016; 54(2):504-15. doi: 10.1007/s12020-016-1019-1.
9. Layton JB, Li D, Meier CR, Sharpless JL, Stürmer T, Brookhart MA. Injection testosterone and adverse cardiovascular events: A case-crossover analysis. Clin Endocrinol (Oxf). 2018;88(5):719-27. doi: 10.1111/cen.13574.
10. Mehrabi M, Kazemzadeh Y, Gorzi A, Hosseini SA, Sedaghati S. The Effect of Eight Weeks of Testosterone Enanthate Consumption on Oxidative Indicators of Kidney Tissue in Resistance Trained Rats. 2020; 5(4):155-9. doi: 10.34172/ijbsm.2020.27.
11. Albano GD, Amico F, Cocimano G, Liberto A, Maglietta F, Esposito M, Rosi GL, Di Nunno N, Salerno M, Montana A. Adverse Effects of Anabolic-Androgenic Steroids: A Literature Review. 2021; 9(1): 97.
12. Tsametis CP, Isidori AM. Testosterone replacement therapy: For whom, when and how? Metabolism. 2018; 86: 69-78. doi: 10.1016/j.metabol.2018.03.007.
13. Petering RC, Brooks NA. Testosterone Therapy: Review of Clinical Applications. Am Fam Physician. 2017; 96(7): 441-9.
14. Osterberg EC, Bernie AM, Ramasamy R. Risks of testosterone replacement therapy in men. Indian J Urol. 2014; 30(1): 2-7. doi: 10.4103/0970-1591.124197.
15. Howatson G, McHugh MP, Hill JA, Brouner J, Jewell AP, van Someren KA, Shave RE, Howatson SA. Influence of tart cherry juice on indices of recovery following marathon running. Scand J Med Sci Sports. 2010;20(6):843-52. doi: 10.1111/j.1600-0838.2009.01005.x.
16. Levers K, Dalton R, Galvan E, O'Connor A, Goodenough C, Simbo S, et al. Effects of powdered Montmorency tart cherry supplementation on acute endurance exercise performance in aerobically trained individuals. J Int Soc Sports Nutr. 2016;13:22. doi: 10.1186/s12970-016-0133-z.
17. Stefanescu R, Tero-Vescan A, Negroiu A, Aurica E, Vari CE. A Comprehensive Review of the Phytochemical, Pharmacological, and Toxicological Properties of Tribulus terrestris L. Biomolecules. 2020;10(5). doi: 10.3390/biom10050752.
18. Smith SJ, Lopresti AL, Teo SYM, Fairchild TJ. Examining the Effects of Herbs on Testosterone Concentrations in Men: A Systematic Review. Advances in nutrition (Bethesda, Md). 2020. doi: 10.1093/advances/nmaa134.
19. Chauhan NS, Sharma V, Dixit VK, Thakur M. A Review on Plants Used for Improvement of Sexual Performance and Virility. BioMed Res Int 2014; 2014: 868062. doi: 10.1155/2014/868062.
20. Mehraban F, Jafari M, Akbartabar Toori M, Sadeghi H, Joodi B, Mostafazade M, Sadeghi H. Effects of date palm pollen (Phoenix dactylifera L.) and Astragalus ovinus on sperm parameters and sex hormones in adult male rats. Iran J Reproductive Med 2014; 12(10):705-12.
21. Elblehi SS, El-Sayed YS, Soliman MM, Shukry M. Date Palm Pollen Extract Avert Doxorubicin-Induced Cardiomyopathy Fibrosis and Associated Oxidative/Nitrosative Stress, Inflammatory Cascade, and Apoptosis-Targeting Bax/Bcl-2 and Caspase-3 Signaling Pathways. Animals: an open access journal from MDPI. 2021; 11(3). doi: 10.3390/ani11030886.
22. Vitale K, Getzin A. Nutrition and Supplement Update for the Endurance Athlete: Review and Recommendations. Nutrients. 2019; 11(6). doi: 10.3390/nu11061289.
23. Maky MA, Sadek M, Shanab O, Mahmoud HAM, Rehan IF. Nutritional characterization of various classes of Egyptian beef luncheon. J Advanced Veterinary Animal Res 2020; 7(2):299-307. doi: 10.5455/javar.2020.g421.
24. Mahran GH, Abdel-Wahab SM, Attia AM. A phytochemical study of date palm pollen. Planta medica. 1976; 29(2): 171-5. doi: 10.1055/s-0028-1097648.
25. Abbas FA, Ateya AM. Estradiol, esteriol, estrone and novel flavonoids from date palm pollen. Australian J Basic Appl Sci 2011; 5(8):606-14.
26. Maunder A, Bessell E, Lauche R, Adams J, Sainsbury A, Fuller NR. Effectiveness of herbal medicines for weight loss: A systematic review and meta-analysis of randomized controlled trials. Diabetes, Obesity Metabol 2020; 22(6):891-903. doi: 10.1111/dom.13973.
27. Liu Y, Sun M, Yao H, Liu Y, Gao R. Herbal Medicine for the Treatment of Obesity: An Overview of Scientific Evidence from 2007 to 2017. Evidence-Based Complementary and Alternative Medicine. 2017; 2017: 8943059. doi: 10.1155/2017/8943059.
28. Shirvani H, Ghanbari-Niaki A, Rahmati-Ahmadabad S, Sobhani VJIJoAEP. Effects of endurance training and herb supplementation on tissue nesfatin-1/nucleobindin-2 and ghrelin mRNA expression. 2017; 6(1):72-85.
29. Zarezadehmehrizi A, Hong J, Lee J, Rajabi H, Gharakhanlu R, Naghdi N, Azimi M, Park Y. Exercise training ameliorates cognitive dysfunction in amyloid beta-injected rat model: possible mechanisms of Angiostatin/VEGF signaling. Metabolic Brain Disease. 2021;36(8):2263-71. doi: 10.1007/s11011-021-00751-2.
30. Park Y, Aminizadeh S, Lee J, Zarezadehmehrizi A, Najafipour H, Amiri‐Deh Ahmadi M, Moflehi D, Rashidzadeh HJTFJ. MitoQ supplementation improves oxygen uptake kinetic by reduced reactive oxygen species levels and altered expression of miR‐155 and miR‐181b. 2022;36.
31. Lee J, Zarezadehmehrizi A, Hong J, Park YJFJOPotFoASfEB. Exercise Training Alleviates Alzheimer's Disease-Associated Aortic Endothelial Dysfunction. 2022;36.
32. Arbati A, Matinhomaee H, Azarbayjani MA, Rahmati-Ahmadabad S. Effect of Resistance Training, Testosterone, and Phoenix dactylifera on Gene Expression of Adiponectin and GLUT4 and Oxidative Stress Markers in Adipose Tissue of Rats. J Mazandaran Univ Med Sci 2021; 31(203):39-49.
33. Korta P, Pocheć E, Mazur-Biały A. Irisin as a Multifunctional Protein: Implications for Health and Certain Diseases. 2019; 55(8):485.
34. Arias-Loste MT, Ranchal I, Romero-Gómez M, Crespo J. Irisin, a Link among Fatty Liver Disease, Physical Inactivity and Insulin Resistance. 2014; 15(12):23163-78.
35. Gulick CN, Peddie MC, Jowett T, Hackney AC, Rehrer NJ. Exercise, Dietary Protein, and Combined Effect on IGF-1. Int J Sci Res Methodol 2020; 16(3): 61-77.
36. Srinivasa S, Suresh C, Mottla J, Hamarneh SR, Irazoqui JE, Frontera W, et al. FNDC5 relates to skeletal muscle IGF-I and mitochondrial function and gene expression in obese men with reduced growth hormone. Growth Horm IGF Res. 2016; 26:36-41. doi: 10.1016/j.ghir.2015.12.008.
37. Huh JY, Panagiotou G, Mougios V, Brinkoetter M, Vamvini MT, Schneider BE, Mantzoros CS. FNDC5 and irisin in humans: I. Predictors of circulating concentrations in serum and plasma and II. mRNA expression and circulating concentrations in response to weight loss and exercise. Metabolism. 2012; 61(12): 1725-38. doi: 10.1016/j.metabol.2012.09.002.
38. Shirvani H, Rahmati-Ahmadabad S, Broom DR, Mirnejad R. Eccentric resistance training and β-hydroxy-β-methylbutyrate free acid affects muscle PGC-1α expression and serum irisin, nesfatin-1 and resistin in rats. J Experimental Biol 2019;222(10):jeb198424. doi: 10.1242/jeb.198424..
39. Jiheel MJ, Arrak JK. Role of DPP (Phoenix dactylifera L.) extract on ameliorating The incidence of hemoglobinoxidation induced by sodium nitrite. Kufa J Veterinary Med Sci 2015;6(2). doi:
40. Chodari L, Mohammadi M, Ghorbanzadeh V, Dariushnejad H, Mohaddes G. Testosterone and Voluntary Exercise Promote Angiogenesis in Hearts of Rats with Diabetes by Enhancing Expression of VEGF-A and SDF-1a. Can J Diabetes. 2016; 40(5):436-41. doi: 10.1016/j.jcjd.2016.03.004.
41. Rahmati-Ahmadabad S, Azarbayjani MA, Farzanegi P, Moradi L. High-intensity interval training has a greater effect on reverse cholesterol transport elements compared with moderate-intensity continuous training in obese male rats. Eur J Preventive Cardiol 2019: 2047487319887828. doi: 10.1177/2047487319887828.
42. Rahmati-Ahmadabad S, Azarbayjani M-A, Broom DR, Nasehi M. Effects of high-intensity interval training and flaxseed oil supplement on learning, memory and immobility: relationship with BDNF and TrkB genes. 2021;17(3):273-83. doi: 10.3920/cep200046.
43. Albert FW, Bloom JS, Siegel J, Day L, Kruglyak L. Genetics of trans-regulatory variation in gene expression. eLife. 2018;7. doi: 10.7554/eLife.35471.
44. Saito T, Whatmore P, Taylor JF, Fernandes JMO, Adam AC, Tocher DR, Espe M, Skjærven KH. Micronutrient supplementation affects transcriptional and epigenetic regulation of lipid metabolism in a dose-dependent manner. Epigenetics. 2021; 16(11): 1217-34. doi: 10.1080/15592294.2020.1859867.
45. Karoly HC, Stevens CJ, Magnan RE, Harlaar N, Hutchison KE, Bryan AD. Genetic Influences on Physiological and Subjective Responses to an Aerobic Exercise Session among Sedentary Adults. J Cancer Epidemiol 2012; 2012: 540563. doi: 10.1155/2012/540563.
46. Leońska-Duniec A, Ahmetov, II, Zmijewski P. Genetic variants influencing effectiveness of exercise training programmes in obesity - an overview of human studies. Biol Sport 2016; 33(3):207-14. doi: 10.5604/20831862.1201052.
47. Maleki F, Ovens K, McQuillan I, Kusalik AJ. Size matters: how sample size affects the reproducibility and specificity of gene set analysis. Human genomics. 2019; 13(Suppl 1):42. doi: 10.1186/s40246-019-0226-2.
48. Cao RY, Zheng H, Redfearn D, Yang J. FNDC5: A novel player in metabolism and metabolic syndrome. Biochimie. 2019; 158: 111-6. doi: https://doi.org/10.1016/j.biochi.2019.01.001.
49. Vecchiato M, Zanardo E, Battista F, Quinto G, Bergia C, Palermi S, Duregon F, Ermolao A, Neunhaeuserer D. The Effect of Exercise Training on Irisin Secretion in Patients with Type 2 Diabetes: A Systematic Review. Journal of clinical medicine. 2022; 12(1). doi: 10.3390/jcm12010062.
50. Zunner BEM, Wachsmuth NB, Eckstein ML, Scherl L, Schierbauer JR, Haupt S, Stumpf C, Reusch L, Moser O. Myokines and Resistance Training: A Narrative Review. 2022;23(7):3501. doi:
51. Shirvani H, Rahmati-Ahmadabad S, Kowsari E, Fry H, Kazemi M, Kaviani M. Effects of 2-week HMB-FA supplementation with or without eccentric resistance exercise on expression of some genes related to muscle protein turnover and serum irisin and IGF-1 concentrations. Gene. 2020;760:145018. doi: https://doi.org/10.1016/j.gene.2020.145018.
52. Tsuchiya Y, Mizuno S, Goto K. Irisin response to downhill running exercise in humans. J Exerc Nutr Biochem 2018; 22(2): 12-7. doi: 10.20463/jenb.2018.0011.
53. Fox J, Rioux BV, Goulet EDB, Johanssen NM, Swift DL, Bouchard DR, Loewen H, Senechal M. Effect of an acute exercise bout on immediate post-exercise irisin concentration in adults: A meta-analysis. Scand J Med Sci Sports. 2018;28(1):16-28. doi: 10.1111/sms.12904.
54. Pekkala S, Wiklund PK, Hulmi JJ, Ahtiainen JP, Horttanainen M, Pollanen E, Makela KA, Kainulainen H, Hakkinen K, Nyman K, Alen M, Herzig KH, Cheng S. Are skeletal muscle FNDC5 gene expression and irisin release regulated by exercise and related to health? J Physiol. 2013; 591(21): 5393-400. doi: 10.1113/jphysiol.2013.263707.
55. Rodríguez-Gutiérrez E, Torres-Costoso A, Pascual-Morena C, Pozuelo-Carrascosa DP, Garrido-Miguel M, Martínez-Vizcaíno V. Effects of Resistance Exercise on Neuroprotective Factors in Middle and Late Life: A Systematic Review and Meta-Analysis. Aging and disease. 2023;14(4):1264-75. doi: 10.14336/ad.2022.1207.
56. Choobineh S, Akbarnejad A, Kakavand V, Yari M. Comparison of growth hormone and insulin-like growth factor-1 responses to high intensity and low intensity resistance training with and without blood flow restriction in adolescent male athletes. 2019; 41(4):40-8. doi: 10.34172/mj.2019.044.
57. Dieli-Conwright CM, Kiwata JL, Tuzon CT, Spektor TM, Sattler FR, Rice JC, Schroeder ET. Acute Response of PGC-1alpha and IGF-1 Isoforms to Maximal Eccentric Exercise in Skeletal Muscle of Postmenopausal Women. J Strength Cond Res. 2016; 30(4): 1161-70. doi: 10.1519/JSC. 0000000000001171.
58. Zebrowska A, Waskiewicz Z, Zajac A, Gasior Z, Galbo H, Langfort J. IGF-1 response to arm exercise with eccentric and concentric muscle contractions in resistance-trained athletes with left ventricular hypertrophy. Int J Sports Med. 2013;34(2):116-22. doi: 10.1055/s-0032-1321720.
59. Townsend JR, Hoffman JR, Gonzalez AM, Jajtner AR, Boone CH, Robinson EH, Mangine GT, Wells AJ, Fragala MS, Fukuda DH, Stout JR. Effects of beta-Hydroxy-beta-methylbutyrate Free Acid Ingestion and Resistance Exercise on the Acute Endocrine Response. Int J Endocrinol. 2015; 2015: 856708. doi: 10.1155/2015/856708.
60. Jiang Q, Lou K, Hou L, Lu Y, Sun L, Tan SC, Low TY, Kord-Varkaneh H, Pang S. The effect of resistance training on serum insulin-like growth factor 1(IGF-1): A systematic review and meta-analysis. Complementary Therapies in Medicine. 2020;50:102360. doi: https://doi.org/10.1016/j.ctim. 2020.102360.
61. Shehzad M, Rasheed H, Naqvi SA, Al-Khayri JM, Lorenzo JM, Alaghbari MA, Manzoor MF, Aadil RM. Therapeutic Potential of Date Palm against Human Infertility: A Review. Metabolites. 2021; 11(6). doi: 10.3390/metabo11060408.
62. Tahvilzadeh M, Hajimahmoodi M, Rahimi R. The Role of Date Palm (Phoenix dactylifera L) Pollen in Fertility:A Comprehensive Review of Current Evidence. 2016; 21(4): 320-4. doi: 10.1177/2156587215609851.
63. Selmani C, Chabane D, Bouguedoura N. Ethnobotanical survey of phoenix dactylifera l. pollen used for the treatment of infertility problems in algerian oases. Afr J Tradit Complement Altern Med. 2017; 14(3): 175-86. doi: 10.21010/ajtcam.v14i3.19.
64. Karasawa K, Uzuhashi Y, Hirota M, Otani H. A matured fruit extract of date palm tree (Phoenix dactylifera L.) stimulates the cellular immune system in mice. J Agricultural Food Chem 2011; 59(20):11287-93. doi: 10.1021/jf2029225.
65. Jahromi AR, Mosallanezhad Z, Hosini FS, Jamali S, Sharifi N. The effect of date palm on sexual function in infertile couples: a double-blind controlled clinical trial. BMC Res Notes 2022; 15(1):55. doi: 10.1186/s13104-022-05945-0.
66. Habib HM, El-Fakharany EM, El-Gendi H, El-Ziney MG, El-Yazbi AF, Ibrahim WH. Palm Fruit (Phoenix dactylifera L.) Pollen Extract Inhibits Cancer Cell and Enzyme Activities and DNA and Protein Damage. Nutrients. 2023; 15(11). doi: 10.3390/nu15112614.
67. Assyov Y, Gateva A, Karamfilova V, Gatev T, Nedeva I, Velikova T, Kamenov ZA. Impact of testosterone treatment on circulating irisin in men with late-onset hypogonadism and metabolic syndrome. Aging Male. 2020:1-7. doi: 10.1080/13685538.2020.1770721.
68. Hobbs CJ, Plymate SR, Rosen CJ, Adler RA. Testosterone administration increases insulin-like growth factor-I levels in normal men. J Clin Endocrinol Metab. 1993; 77(3): 776-9. doi: 10.1210/jcem.77.3.7690364.
ارسال پیام به نویسنده مسئول

ارسال نظر درباره این مقاله
نام کاربری یا پست الکترونیک شما:

CAPTCHA



XML   English Abstract   Print


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

Arbati A, Matinhomaee H, Azarbayjani M A, Rahmati S. The effects of resistance training, testosterone and palm (Phoenix dactylifera L.) pollen extract on the expression of FNDC5 and IGF1 genes in brown adipose tissue in male rats. Feyz Med Sci J 2023; 27 (5) :481-492
URL: http://feyz.kaums.ac.ir/article-1-4755-fa.html

اربطی علی، متین همایی حسن، آذربایجانی محمدعلی، رحمتی صالح. اثرات تمرین مقاومتی، تستوسترون و عصاره گرده نخل (Phoenix dactylifera L.) بر بیان ژن‌های FNDC5 و IGF1 بافت چربی قهوه‌ای در موش‌های صحرایی نر. مجله علوم پزشکی فيض. 1402; 27 (5) :481-492

URL: http://feyz.kaums.ac.ir/article-1-4755-fa.html



Creative Commons License
This open access journal is licensed under a Creative Commons Attribution-NonCommercial ۴.۰ International License. CC BY-NC ۴. Design and publishing by Kashan University of Medical Sciences.
Copyright ۲۰۲۳© Feyz Medical Sciences Journal. All rights reserved.
دوره 27، شماره 5 - ( دوماه نامه 1402 ) برگشت به فهرست نسخه ها
مجله علوم پزشکی فیض Feyz Medical Sciences Journal
Persian site map - English site map - Created in 0.08 seconds with 46 queries by YEKTAWEB 4700