Volume 31, Issue 3 (June 2020)                   Studies in Medical Sciences 2020, 31(3): 169-177 | Back to browse issues page

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Gilani A, Gaeini A, Nouri R. EFFECT OF AEROBIC EXERCISE TRAINING AND OZONE THERAPY ON TRF2 AND TERT GENE EXPRESSIONS IN HEART TISSUE OF RATS WITH OSTEOARTHRITIS. Studies in Medical Sciences 2020; 31 (3) :169-177
URL: http://umj.umsu.ac.ir/article-1-5009-en.html
Department of Exercise Physiology, University of Tehran, Kish International Campus, Tehran, Iran (Corresponding Author) , nuri_r7@ut.ac.ir
Abstract:   (3277 Views)
Background & Aims: Osteoarthritis (OA) is the most common disease of joints caused by the degradation of articular cartilage and subchondral bone. It is unknown whether different therapies exert differential cellular effects. Telomeres and telomerase play a major role in cellular aging with implications for global health. Also, OA may be associated with CVD and reduction in telomeres length. Thus, this study investigated the effect of ozone therapy and aerobic training on telomeres and telomerase expression genes in the heart of rats with knee OA.
Materials & Methods: In this experimental study, knee OA was induced by the surgical method in rats. OA rats were randomly divided into the OA, OA and ozone therapy (OAO), and OA and aerobic exercise (OAE) groups. Rats in the OAO group received O3 at the concentration of 20μg/ml, once a week for 3 weeks. Rats in the OAE group were trained on rodent treadmill with intensity of 16 m/min, 3 days/week. 48 hours after the intervention, cartilage and heart tissues were isolated and the expression of TRF2 and TERT gene was measured using Real-Time qPCR (RT-qPCR).
Results: OAE significantly increased the expression of TRF2 compared to the OA (p=0.045) group. Also, OAE group had significantly higher expression of TERT compared to the control (p= 0.02) group but no difference was observed between OA and OAO in TRF2 (p=0.303) and TERT (p=0.382) genes expression.
Conclusion: TRF2 and TERT increased after 8 weeks of aerobic exercise compared to the Ozone therapy.
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Type of Study: Research | Subject: Exercise physiology

References
1. AlKuwaity, K.W., et al., Prevalence and Determinant Factors of Osteoarthritis of the Knee Joint among Elderly in Arar, KSA. The Egyptian Journal of Hospital Medicine (July 2018), 2018. 72(9): p. 5173-5177. [DOI:10.21608/ejhm.2018.10737]
2. Eskandari-Nasab, E., et al., Telomere and telomerase: From discovery to cancer treatment. Gene, Cell and Tissue, 2015. 2(3). [DOI:10.17795/gct28084]
3. Rahman, M.M., et al., The relationship between osteoarthritis and cardiovascular disease in a population health survey: a cross-sectional study. BMJ open, 2013. 3(5): p. e002624. [DOI:10.1136/bmjopen-2013-002624] [PMID] [PMCID]
4. Booth, S.A. and F.J. Charchar, Cardiac telomere length in heart development, function, and disease. Physiological Genomics, 2017. 49(7): p. 368-384. [DOI:10.1152/physiolgenomics.00024.2017] [PMID]
5. Kunduracilar, Z. and K. Selici, Cardiovascular and Functional Capacity of Patients with Knee Osteoarthritis, in Osteoarthritis. 2018, IntechOpen. [DOI:10.5772/intechopen.81680] [PMCID]
6. Noorimofrad, S., The effect of high intensity interval training on telomere length and telomerase activity in non-athlete young men. Journal of Basic Research in Medical Sciences, 2018. 5(2): p. 1-7. [DOI:10.29252/jbrms.5.2.1]
7. Mosallanezhad, Z., et al., The effect of high-intensity interval training on telomere length of leukocytes in sedentary young women. Advances in Environmental Biology, 2014: p. 841-846. [URL]
8. Kuszel, L., et al., Osteoarthritis and telomere shortening. Journal of applied genetics, 2015. 56(2): p. 169-176. [DOI:10.1007/s13353-014-0251-8] [PMID] [PMCID]
9. Fernandez-Cuadros, M.E., et al., Mid-Term Effectiveness of Ozone (O2-O3) Compared to Platelet-Rich Plasma (PRP) in the Management of Knee Osteoarthritis: A Randomized Parallel Controlled Trial. 2019. [DOI:10.5812/mejrh.74140]
10. Hossein Mirkarimpour, S., et al., The Effect of 4-week Swimming Training on Rat's Knee Osteoarthritis induced by Monosodium Iodoacetate. Razi Journal of Medical Sciences, 2013. 19(104). [Google Scholar]
11. AKBARI, B.H., A.A. RAVASI, and M.R. AKBARI, THE EFFECT OF A ENDURANCE TRAINING PERIOD WITH CELLULAR ANTI-AGING PURPOSE ON TELOMERASE ENZYME CONTENT IN CARDIAC TISSUE AND PERIPHERAL BLOOD LYMPHOCYTES IN RATS. 2017. [URL]
12. نوروزي کمره, م.ح., et al., Effect of 12 weeks aerobic training and oral green tea extract on cardiac caspase-3 expression in aged male rats. نشريه علوم زيستي ورزشي, 2018. 10(2): p. 221-235. [Google Scholar]
13. Werner, C.M., et al., Differential effects of endurance, interval, and resistance training on telomerase activity and telomere length in a randomized, controlled study. European heart journal, 2018. 40(1): p. 34-46. [DOI:10.1093/eurheartj/ehy585] [PMID] [PMCID]
14. Ludlow, A.T., et al., Exercise alters mRNA expression of telomere-repeat binding factor 1 in skeletal muscle via p38 MAPK. Journal of applied physiology, 2012. 113(11): p. 1737-1746. [DOI:10.1152/japplphysiol.00200.2012] [PMID] [PMCID]
15. Assis, L., et al., Aerobic exercise training and low-level laser therapy modulate inflammatory response and degenerative process in an experimental model of knee osteoarthritis in rats. Osteoarthritis and cartilage, 2016. 24(1): p. 169-177. [DOI:10.1016/j.joca.2015.07.020] [PMID]
16. Stellos, K. and I. Spyridopoulos, Exercise, telomerase activity, and cardiovascular disease prevention. European heart journal, 2019. [DOI:10.1093/eurheartj/ehy707] [PMID]
17. Tucker, L.A., Physical activity and telomere length in US men and women: An NHANES investigation. Preventive medicine, 2017. 100: p. 145-151. [DOI:10.1016/j.ypmed.2017.04.027] [PMID]
18. Du, M., et al., Physical activity, sedentary behavior, and leukocyte telomere length in women. American journal of epidemiology, 2012. 175(5): p. 414-422. [DOI:10.1093/aje/kwr330] [PMID] [PMCID]
19. Santoso, D.I.S., et al., The effect of aerobic exercise on relative leukocyte telomere length in male Sprague-Dawley rats given a high fat-diet. F1000Research, 2018. 7. [DOI:10.12688/f1000research.15127.1]
20. Control, C.f.D. and Prevention, NCHS research ethics review board (ERB) approval. National Center for Health Statistics. Available: http://www. cdc. gov/nchs/nhanes/irba98. htm. Accessed, 2012. 20. [URL]
21. Bär, C., et al., Telomerase expression confers cardioprotection in the adult mouse heart after acute myocardial infarction. Nature communications, 2014. 5: p. 5863. [DOI:10.1038/ncomms6863] [PMID] [PMCID]
22. Ait-Aissa, K., et al., Telomerase deficiency predisposes to heart failure and ischemia-reperfusion Injury. Frontiers in cardiovascular medicine, 2019. 6: p. 31. [DOI:10.3389/fcvm.2019.00031] [PMID] [PMCID]
23. Azabijani, M., The Effects of an 8-Week Resistance-Interval Training on the Telomere Length, Telomerase Activity, and TRF2 Expression in Sedentary Young Men. Community Health Journal, 2017. 11(شماره): p. 76-85. [URL]
24. Brown, L., B. Needham, and J. Ailshire, Telomere length among older US adults: differences by race/ethnicity, gender, and age. Journal of aging and health, 2017. 29(8): p. 1350-1366. [DOI:10.1177/0898264316661390] [PMID] [PMCID]
25. Control, C.f.D. and Prevention, NHANES questionnaires, datasets, and related documentation. 2011.
26. Marcon, F., et al., Diet-related telomere shortening and chromosome stability. Mutagenesis, 2011. 27(1): p. 49-57. [DOI:10.1093/mutage/ger056] [PMID] [PMCID]
27. Lee, J., et al., Association between dietary patterns in the remote past and telomere length. European journal of clinical nutrition, 2015. 69(9): p. 1048. [DOI:10.1038/ejcn.2015.58] [PMID]
28. Kyu, H.H., et al., Physical activity and risk of breast cancer, colon cancer, diabetes, ischemic heart disease, and ischemic stroke events: systematic review and dose-response meta-analysis for the Global Burden of Disease Study 2013. bmj, 2016. 354: p. i3857. [DOI:10.1136/bmj.i3857] [PMID] [PMCID]
29. Johnson, C.L., et al., National health and nutrition examination survey. Analytic guidelines, 1999-2010. 2013. [Google Scholar]
30. Seyam, O., et al., Clinical utility of ozone therapy for musculoskeletal disorders. Medical gas research, 2018. 8(3): p. 103. [DOI:10.4103/2045-9912.241075] [PMID] [PMCID]
31. Di Filippo, C., et al., Daily oxygen/O3 treatment reduces muscular fatigue and improves cardiac performance in rats subjected to prolonged high intensity physical exercise. Oxidative Medicine and Cellular Longevity, 2015. 2015. [DOI:10.1155/2015/190640] [PMID] [PMCID]
32. Di Filippo, C., et al., Acute oxygen-ozone administration to rats protects the heart from ischemia reperfusion infarct. Inflammation Research, 2008. 57(10): p. 445-449. [DOI:10.1007/s00011-008-7237-0] [PMID]
33. Smith, A.J., et al., Ozone Therapy: a critical physiological and diverse clinical evaluation with regard to immune modulation, anti-infectious properties, anti-cancer potential, and impact on anti-oxidant enzymes. Open Journal of Molecular and Integrative Physiology, 2015. 5(03): p. 37. [DOI:10.4236/ojmip.2015.53004]

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