دوره 9، شماره 2 - ( 2-1400 )                   جلد 9 شماره 2 صفحات 154-145 | برگشت به فهرست نسخه ها


XML Print


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

Shahbazi M, Behpoor N, Faramarzi M, Banitalebi E. The Effect of High- and Moderate-intensity Endurance Training on Some Anabolic/Catabolic Osteokines in Old Male Wistar Rats. Res Mol Med (RMM) 2021; 9 (2) :145-154
URL: http://rmm.mazums.ac.ir/article-1-426-fa.html
The Effect of High- and Moderate-intensity Endurance Training on Some Anabolic/Catabolic Osteokines in Old Male Wistar Rats. Research in Molecular Medicine. 1400; 9 (2) :145-154

URL: http://rmm.mazums.ac.ir/article-1-426-fa.html


چکیده:   (2104 مشاهده)
Background: Bone-related osteokines are crucial for bone function and metabolic response to physical activity. The present study aimed to shed light on the effect of different intensities of continuous and interval endurance training on the serum levels of some osteokines that are associated with wingless-related integration site (WNT) signaling pathway and Receptor Activator of Nuclear Factor (NF)-κB Ligand (RANKL) in old male Wistar rats.
Materials and Methods: A total of 24 old male Wistar rats (mean age: 23 months, mean weight: 437.93 g) were randomly assigned to three groups: interval endurance-training group (n=8), continuous endurance-training group (n=8), and control group (n=8). The continuous and interval training interventions comprised 8 weeks of treadmill exercise, 5 days a week. The continuous endurance-training group started to exercise at 60% of velocity at maximal oxygen uptake (vVO2max) for 16 min during the first week. It continued with 70% of vVO2max for 45 min from the fourth week onward. In contrast, the interval endurance-training group switched on exercise with 40%-80% of vVO2max from the first week and persisted with 30%-110% of vVO2max from the fourth week onward. As the exercise bout was completed, the enzyme-linked immunosorbent assay was applied to measure the study dependent variables. Statistical analysis was further performed using 1-way analysis of variance, considering the significance level of P≤0.05.
Results: The study results demonstrated a significant difference in the levels of Oteoprotegerin (OPG) (P=0.036) and RANKL (P=0.001) in the experimental (namely, interval and continuous training) groups compared with the controls following the exercise bout. However, the level of sclerostin was not significantly changed (P=0.549).
Conclusion: High-intensity endurance training in the RANKL/OPG and WNT pathways decreased sclerostin and RANKL levels, but this decrease was significant at the RANKL level. It was effective with regard to the intensities of different types of endurance exercise.
متن کامل [PDF 879 kb]   (464 دریافت)    
نوع مطالعه: پژوهشي | موضوع مقاله: فيزيولوژي
انتشار: 1400/2/30

فهرست منابع
1. Boskey, A.L. and R. Coleman, Aging and bone. Journal of dental research, 2010. 89(12): p. 1333-1348. [DOI:10.1177/0022034510377791] [PMID] [PMCID]
2. Tommasini, S.M., P. Nasser, and K.J. Jepsen, Sexual dimorphism affects tibia size and shape but not tissue-level mechanical properties. Bone, 2007. 40(2): p. 498-505. [DOI:10.1016/j.bone.2006.08.012] [PMID]
3. Bonewald, L.F., The amazing osteocyte. Journal of bone and mineral research, 2011. 26(2): p. 229-238. [DOI:10.1002/jbmr.320] [PMID] [PMCID]
4. Bijeh, N., et al., Effect of aerobic exercises on markers of bone metabolism in middle-aged women. Kowsar Medical Journal, 2011. 16(2): p. 129-135.
5. Frost, H., The biology of fracture healing. An overview for clinicians. Part II. Clinical orthopaedics and related research, 1989(248): p. 294-309. [DOI:10.1097/00003086-198911000-00046]
6. Ellies, D.L., et al., Bone density ligand, Sclerostin, directly interacts with LRP5 but not LRP5G171V to modulate Wnt activity. Journal of Bone and Mineral Research, 2006. 21(11): p. 1738-1749. [DOI:10.1359/jbmr.060810] [PMID]
7. Schoppet, M., K.T. Preissner, and L.C. Hofbauer, RANK ligand and osteoprotegerin: paracrine regulators of bone metabolism and vascular function. Arteriosclerosis, thrombosis, and vascular biology, 2002. 22(4): p. 549-553. [DOI:10.1161/01.ATV.0000012303.37971.DA] [PMID]
8. Niu, T. and C.J. Rosen, The insulin-like growth factor-I gene and osteoporosis: a critical appraisal. Gene, 2005. 361: p. 38-56. [DOI:10.1016/j.gene.2005.07.016] [PMID]
9. Jilka, R.L. and C.A. O'Brien, The role of osteocytes in age-related bone loss. Current osteoporosis reports, 2016. 14(1): p. 16-25. [DOI:10.1007/s11914-016-0297-0] [PMID]
10. Brahm H, Piehl - Aulin K, Liunghall S. Bone Metabolism during Exercise and Recovery:The influence of plasona volume and physical Fithness. J Am Geratr soc. 1996. p. 756-62.
11. Palmas S , Hinton R, Scohrector T, Thomas R. weight-bearing aerobic exercise increase markers of bone formation during short term weight loss in overweight and oboes men and woman. J Metabolism. 2006. p.1616-1618. [DOI:10.1016/j.metabol.2006.07.023] [PMID]
12. Gianni F, Maddalozzo et al. The effect of hormone replacement therapy and resistance training on spine bone mineral density postmenopausal women.bone. 2006. p. 1244-125. [DOI:10.1016/j.bone.2006.12.059] [PMID]
13. Marques, E.A., et al., Effects of resistance and aerobic exercise on physical function, bone mineral density, OPG and RANKL in older women. Experimental gerontology, 2011. 46(7): p. 524-532. [DOI:10.1016/j.exger.2011.02.005] [PMID]
14. West, S.L., J.L. Scheid, and M.J. De Souza, The effect of exercise and estrogen on osteoprotegerin in premenopausal women. Bone, 2009. 44(1): p. 137-144. [DOI:10.1016/j.bone.2008.09.008] [PMID]
15. Shimamura, C., et al., Effect of decreased physical activity on bone mass in exercise-trained young rats. Journal of orthopaedic science, 2002. 7(3): p. 358-363. [DOI:10.1007/s007760200060] [PMID]
16. Sinaki, M., et al., Three-year controlled, randomized trial of the effect of dose-specified loading and strengthening exercises on bone mineral density of spine and femur in nonathletic, physically active women. Bone, 1996. 19(3): p. 233-244. [DOI:10.1016/8756-3282(96)00174-3]
17. Turner, C., Functional determinants of bone structure: beyond Wolff's law of bone transformation. 1992, Elsevier. [DOI:10.1016/8756-3282(92)90082-8]
18. Banfi, G., M. Corsi, and E. Galliera, Osteoprotegerin, RANK and RANKL are not modified by acute exercise in elite rugby players. The Journal of sports medicine and physical fitness, 2012. 52(2): p. 198-201.
19. Aido, M.I.F.d., The Influence of Age and Mechanical Loading on Bone Structure and Material Properties. 2015, Technische Universität Berlin.
20. Marques, E.A., et al., Response of bone mineral density, inflammatory cytokines, and biochemical bone markers to a 32-week combined loading exercise programme in older men and women. Archives of Gerontology and Geriatrics, 2013. 57(2): p. 226-233. [DOI:10.1016/j.archger.2013.03.014] [PMID]
21. Bailey C, Brooke-Wavell K. Exercise for optimising peak bone mass in women: Postgraduate symposium. Proceedings of the Nutrition Society. 2008;67(1):9-18. [DOI:10.1017/S0029665108005971] [PMID]
22. Kiuchi A, Shimegi S, Tanaka I, Izumo N, Fukuyama R, Nakamuta H, et al. Dose-response effects of exercise intensity on bone in ovariectomized rats. International Journal of Sport and Health Science. 2006;4:10-8. [DOI:10.5432/ijshs.4.10]
23. Song F, Jiang D, Wang T, Wang Y, Lou Y, Zhang Y, et al. Mechanical stress regulates osteogenesis and adipogenesis of rat mesenchymal stem cells through PI3K/Akt/GSK-3β/β-catenin signaling pathway. BioMed research international. 2017;2017. [DOI:10.1155/2017/6027402] [PMID] [PMCID]
24. Kohrt WM, Bloomfield SA, Little KD, Nelson ME, Yingling VR. Physical activity and bone health. Medicine & Science in Sports & Exercise. 2004;36(11):1985-96. [DOI:10.1249/01.MSS.0000142662.21767.58] [PMID]
25. Leandro CG, Levada AC, Hirabara SM, MANHAS-DE-CASTRO R, De-Castro CB, Curi R, et al. A program of moderate physical training for wistar rats based on maximal oxygen consumption. J Strength Cond Res. 2007;21(3):751-6. https://doi.org/10.1519/00124278-200708000-00016 [DOI:10.1519/R-20155.1] [PMID]
26. Markou KB, Mylonas P, Theodoropoulou A, Kontogiannis A, Leglise M, Vagenakis AG, et al. The influence of intensive physical exercise on bone acquisition in adolescent elite female and male artistic gymnasts. The Journal of Clinical Endocrinology & Metabolism. 2004;89(9):4383-7. [DOI:10.1210/jc.2003-031865] [PMID]
27. Maddalozzo G, Snow C. High intensity resistance training: effects on bone in older men and women. Calcified tissue international. 2000;66(6):399-404. [DOI:10.1007/s002230010081] [PMID]
28. Fahrleitner A, Prenner G, Leb G, TscheliessniggKH, Piswanger-Sölkner C, ObermayerPietsch B,et al. Serum osteoprotegerin is a major determinantof bone density development andprevalentvertebral fracture status following cardiac transplantationBone 2003;32(1):96-106 [DOI:10.1016/S8756-3282(02)00926-2]
29. Cui, S.F., et al., Similar responses of circulating microRNAs to acute high-intensity interval exercise and vigorous-intensity continuous exercise. Frontiers in physiology, 2016. [DOI:10.3389/fphys.2016.00102]
30. Ziegler S, Niessner A, Richter B, Wirth S, Billensteiner E, Woloszczuk W, et al. Endurance running acutely raises plasma osteoprotegerin and lowers plasma receptor activator of nuclear factor κ B ligand. Metabolism. 2005;54(7):935-8. [DOI:10.1016/j.metabol.2005.02.009] [PMID]
31. Gaudio A, Pennisi P, Bratengeier C, Torrisi V, Lindner B, Mangiafico RA,Pulvirenti I, Hawa G, Tringali G, Fiore CE. Increased sclerostin serum levelsassociated with bone formation and resorption markers in patients withimmobilization-induced bone loss. J Clin Endocrinol Metab. 2010;95(5):2248-53. [DOI:10.1210/jc.2010-0067] [PMID]
32. Baron R, Rawadi G 2007 Minireview: targeting the Wnt/-catenin pathway to regulate bone formation in the adult skeleton. Endocrinology 148:2635-2643 [DOI:10.1210/en.2007-0270] [PMID]
33. Ardawi MSM, Al‐Kadi HA, Rouzi AA, Qari MH. Determinants of serum sclerostin in healthy pre‐and postmenopausal women. Journal of Bone and Mineral Research. 2011;26(12):2812-22. [DOI:10.1002/jbmr.479] [PMID]
34. Spatz JM, Fields EE, Yu EW, Divieti Pajevic P, Bouxsein ML, Sibonga JD, ZwartSR, Smith SM. Serum sclerostin increases in healthy adult men during bedrest. J Clin Endocrinol Metab. 2012;97(9):E1736-40. [DOI:10.1210/jc.2012-1579] [PMID] [PMCID]
35. An J, Yang H, Zhang Q, Liu C, Zhao J, Zhang L, et al. Natural products for treatment of osteoporosis: The effects and mechanisms on promoting osteoblast-mediated bone formation. Life sciences. 2016;147:46-58. [DOI:10.1016/j.lfs.2016.01.024] [PMID]
36. Lombardi G, Lanteri P, Colombini A, Mariotti M, Banfi G. Sclerostinconcentrations in athletes: role of load and gender. J Biol Regul HomeostAgents. 2012;26(1):157-63.
37. Sheng Z, Tong D, Ou Y, Zhang H, Zhang Z, Li S, Zhou J, Zhang J, Liao E.Serum sclerostin levels were positively correlated with fat mass and bonemineral density in central south Chinese postmenopausal women. ClinEndocrinol. 2012;76(6):797-801. [DOI:10.1111/j.1365-2265.2011.04315.x] [PMID]
38. Xu XJ, Shen L, Yang YP, Lu FR, Zhu R, Shuai B, Li CG, Wu MX. Serumsclerostin levels associated with lumbar spine bone mineral density andbone turnover markers in patients with postmenopausal osteoporosis. ChinMed J. 2013;126(13):2480-4. [DOI:10.1155/2013/534352] [PMID] [PMCID]
39. Silverman SL. Sclerostin. J Osteoporos. 2010;2010:941419. [DOI:10.4061/2010/941419] [PMID] [PMCID]
40. Compton JT, Lee FY. A review of osteocyte function and the emergingimportance of sclerostin. J Bone Joint Surg Am. 2014;96(19):1659-68. [DOI:10.2106/JBJS.M.01096] [PMID] [PMCID]
41. Shimamura C, Iwamoto J, Takeda T, Ichimura S, Abe H, Toyama Y. Effect of decreased physical activity on bone mass in exercise-trained young rats.J Orthop Sci. 2002;7(3):358-63. [DOI:10.1007/s007760200060] [PMID]
42. Bergström I, Parini P,Gustafsson SA,Andersson G, Brinck J. Physical training increases osteoprotegerin in postmenopausal women. Journal of bone and mineral metabolism. 2012;30(2):202-7. [DOI:10.1007/s00774-011-0304-6] [PMID]
43. Ardawi M-SM, Rouzi AA, Qari MH. Physical activity in relation to serum sclerostin, insulin-like growth factor-1, and bone turnover markers in healthy premenopausal women: a cross-sectional and a longitudinal study. The Journal of Clinical Endocrinology & Metabolism. 2012;97(10):3691-9. [DOI:10.1210/jc.2011-3361] [PMID]
44. Gombos GC, Bajsz V, Pék E, Schmidt B, Sió E, Molics B, et al. Direct effects of physical training on markers of bone metabolism and serum sclerostin concentrations in older adults with low bone mass. BMC Musculoskeletal Disorders. 2016;17(1):254. [DOI:10.1186/s12891-016-1109-5] [PMID] [PMCID]
45. Karaarslan S, Büyükyazi G, Taneli F, Ulman C, Tikiz C, GÜMÜŞER G, et al. Effects of different intensity resistance exercise programs on bone turnover markers, osteoprotegerin and receptor activator of nuclear factor kappa β ligand in post-menopausal women. Turkiye Klinikleri Journal of Medical Sciences. 2010;30(1):123-34. [DOI:10.5336/medsci.2008-8721]
46. Scott JP, Sale C, Greeves JP, Casey A, Dutton J, Fraser WD. The effect of training status on the metabolic response of bone to an acute bout of exhaustive treadmill running. The Journal of Clinical Endocrinology & Metabolism. 2010;95(8):3918-25. [DOI:10.1210/jc.2009-2516] [PMID]
47. Dekker J, Nelson K, Kurgan N, Falk B, Josse A, Klentrou P. Wnt signaling-related osteokines and transforming growth factors before and after a single bout of plyometric exercise in child and adolescent females. Pediatric exercise science. 2017;29(4):504-12. [DOI:10.1123/pes.2017-0042] [PMID]
48. Kim TH, Chang JS, Park K-S, Park J, Kim N, Lee JI, et al. Effects of exercise training on circulating levels of Dickkpof-1 and secreted frizzled-related protein-1 in breast cancer survivors: A pilot single-blind randomized controlled trial. PLoS One. 2017;12(2):e0171771. [DOI:10.1371/journal.pone.0171771] [PMID] [PMCID]
49. Rahimi Saghand M, Rajabi H, Dehkhoda M, Hosseini A. The Effects of Eight Weeks High-Intensity Interval Training vs. Continuous Moderate-Intensity Training on Plasma Dickkopf-1 and Glycemic Control in Patients with Type 2 Diabetes. Annals of Applied Sport Science. 2020;8(2):0-.
50. Salehikiya A. Effect of endurance and resistance training on the improvement of bone: A densitometric and histomorphometric study in male osteoprotic rats. scientific journal of ilam university of medical sciences. 2016;23(7):90-100.
51. Fukumoto S, Martin TJ. Bone as an endocrine organ. Trends in Endocrinology & Metabolism. 2009;20(5):230-6. [DOI:10.1016/j.tem.2009.02.001] [PMID]
52. Capulli M, Paone R, Rucci N. Osteoblast and osteocyte: games without frontiers. Archives of biochemistry and biophysics. 2014;561:3-12. [DOI:10.1016/j.abb.2014.05.003] [PMID]
53. Marks Jr SC, Popoff SN. Bone cell biology: the regulation of development, structure, and function in the skeleton. American Journal of Anatomy. 1988;183(1):1-44. [DOI:10.1002/aja.1001830102] [PMID]
54. Yano K, Tsuda E, Washida N, Kobayashi F,Goto M, Harada A, et al. Immunological characterizationof circulating osteoprotegerin/osteoclastogenesisinhibitory factor: increasedserum concentrations in postmenopausalwomen with osteoporosis. J Bone Miner Res199914(4):518-27. [DOI:10.1359/jbmr.1999.14.4.518] [PMID]
55. Hofbauer LC, Khosla S, Dunstan CR, Lacey DL,Spelsberg TC, Riggs BL. Estrogen stimulates gene expression and protein production of osteoprotegerin in human osteoblastic cells. Endocrinology 1999;140(9):4367-70. [DOI:10.1210/endo.140.9.7131] [PMID]
56. Liu JM, Zhao HY, Ning G, Zhao YJ, Chen Y,Zhang Zh, et al. Relationships between the changes of serum levels of OPG and RANKL with age, menopause, bone biochemical markers and bone mineral density in Chinese women aged 20-75. Calcif Tissue Int 2005;76(1):1-6. [DOI:10.1007/s00223-004-0007-2] [PMID]
57. Indridason OS, Franzson L, Sigurdsson G.Serum osteoprotegerin and its relationship with bone mineral density and markers of bone turnover. Osteoporos Int 2005;16(4):417-23.35. Khosla S, Arrighi HM, Melton LJ 3rd, Atkinson EJ, O'Fallon WM, Dunstan C, et al. Correlates of osteoprotegerin levels in women and men. Osteoporos Int 2002;13(5):394-9. [DOI:10.1007/s001980200045] [PMID]
58. Khosla S, Arrighi HM, Melton LJ 3rd, Atkinson EJ, O'Fallon WM, Dunstan C, et al. Correlates of osteoprotegerin levels in women and men. Osteoporos Int 2002;13(5):394-9. [DOI:10.1007/s001980200045] [PMID]
59. Hinton PS, Rector RS, Thomas TR. Weight-bearing, aerobic exercise increases markers of bone formation during short-term weight loss in overweight and obese men and women. Metabolism. 2006;55(12):1616-8. [DOI:10.1016/j.metabol.2006.07.023] [PMID]
60. Franchimont N, Reenaers C, Lambert C, Belaiche J, Bours V, Malaise M, et al. Increased expression of receptor activator of NF-kappaB ligand (RANKL), its receptor RANK and its decoy receptor osteoprotegerin in the colon of Crohn's disease patients. Clin Exp Immunol 2004;138(3):491-8. [DOI:10.1111/j.1365-2249.2004.02643.x] [PMID] [PMCID]
61. Uemura H, Yasui T, Miyatani Y, Yamada M, Hiyoshi M, Arisawa K, et al. Circulating profiles of osteoprotegerin and soluble receptor activator of nuclear factor kappaB ligand in post-menopausal women. J Endocrinol Invest 2008;31(2):163-8. [DOI:10.1007/BF03345584] [PMID]
62. Mezil YA, Allison D, Kish K, Ditor D, Ward WE, Tsiani E, et al. Response of bone turnover markers and cytokines to high-intensity low-impact exercise. Med Sci Sports Exerc. 2015;47(7):1495-502. [DOI:10.1249/MSS.0000000000000555] [PMID]
63. Kish, Kimberly,Mezil, Yasmeen, Ward, Wendy E., Klentrou, Panagiota, Falk B. Effects of plyometric exercise session on markers of bone turnover in boys and young men. Eur J Appl Physiol. 2015;1-10. [DOI:10.1007/s00421-015-3191-z] [PMID]
64. Oh KW, Rhee EJ, Lee WY, Kim SW, Baek KH, Kang MI, et al. Circulating osteoprotegerin and receptor activator of NF-kappaB ligand system are associated with bone metabolism in middle-aged males. Clin Endocrinol (Oxf) 2005;62(1):92-8. [DOI:10.1111/j.1365-2265.2004.02179.x] [PMID]
65. Herrmann M, Herrmann W. The assessment of bone metabolism in female elite endurance athletes by biochemical bone markers. Clin Chem Lab Med 2004;42(12):1384-9. [DOI:10.1515/CCLM.2004.258] [PMID]
66. Hinton PS, Rector RS, Thomas TR. Weight-bearing, aerobic exercise increases markers of bone formation during short-term weight loss in overweight and obese men and women. Metabolism 2006;55(12):1616-8. [DOI:10.1016/j.metabol.2006.07.023] [PMID]
67. Daniel W.D.West,Nicholas A.Burd Aaron W.Staples. Human exercise-mediated skeletal muscle hypertrophy is an intrinsic process. September 2010, Pages 1371-1375. [DOI:10.1016/j.biocel.2010.05.012] [PMID]
68. Jemtland R, Holden M, Reppe S, Olstad OK, Reinholt FP, Gautvik VT, et al. Molecular disease map of bone characterizing the postmenopausal osteoporosis phenotype. Journal of bone and mineral research. 2011;26(8):1793-801. [DOI:10.1002/jbmr.396] [PMID]
69. Moustafa A, Sugiyama T, Prasad J, Zaman G, Gross T, Lanyon L, et al. Mechanical loading-related changes in osteocyte sclerostin expression in mice are more closely associated with the subsequent osteogenic response than the peak strains engendered. Osteoporosis International. 2012;23(4):1225-34. [DOI:10.1007/s00198-011-1656-4] [PMID] [PMCID]
70. Bilezikian JP. Primer on the metabolic bone diseases and disorders of mineral metabolism: John Wiley & Sons; 2018.
71. Wieczorek-Baranowska A, Nowak A, Pilaczyńska-Szcześniak Ł. Osteocalcin and glucose metabolism in postmenopausal women subjected to aerobic training program for 8 weeks. Metabolism. 2012;61(4):542-5. [DOI:10.1016/j.metabol.2011.08.011] [PMID]

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

بازنشر اطلاعات
Creative Commons License این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است.

کلیه حقوق این وب سایت متعلق به Research in Molecular Medicine می باشد.

طراحی و برنامه نویسی : یکتاوب افزار شرق

© 2024 CC BY-NC 4.0 | Research in Molecular Medicine

Designed & Developed by : Yektaweb