Volume 24, Issue 10 (Jan 2017)                   JSSU 2017, 24(10): 798-809 | Back to browse issues page

XML Persian Abstract Print


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

Farhangi N, Nazem F, Zehsaz F. Effect of Endurance Exercise on Antioxidant Enzyme Activities and Lipid Peroxidation in the Heart of the Streptozotocin-Induced Diabetic Rats. JSSU 2017; 24 (10) :798-809
URL: http://jssu.ssu.ac.ir/article-1-3795-en.html
Abstract:   (9791 Views)

Introduction: Oxidative stress can promote the development of complications of diabetes. Moderate exercise improves cardiac antioxidant status in diabetic animals. The current study aimed to investigate the effect of 8 week endurance exercise training on some heart antioxidant enzyme activities and lipid peroxidation of heart tissue in streptozotocin-induced diabetic rats.

Methods: To this end, 30 male Wistar rats were randomly divided into 3 groups: the healthy control group (C), diabetic control group (DC) and trained diabetic group (TD). Animals in TD group were exercised on a treadmill 4 days a week for 8 weeks. After 8 weeks, superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase (CAT) activities and malondialdehyde (MDA) levels were measured in heart tissues. The data were analyzed using one-way ANOVA (p<0.05).

Results: The CAT and GPx activities of the heart tissue in DC group were found to be significantly higher (p=0.000) in compared with C group, whereas SOD activity was not found significantly different among the experimental groups. Also, heart GPx activity in TD group was significantly lower (p=0.000) than that of DC group, while CAT activity was not affected by endurance training. After 8-week endurance exercise (TD group), the MDA levels of heart tissue were significantly higher (respectively p<0.017 and p=0.000) than C and DC groups.

Conclusion: The results of the present study have demonstrated that due to decreased GPx activities and MDA levels, endurance exercise may make the heart tissue more susceptible to oxidative stress.

Full-Text [PDF 712 kb]   (2817 Downloads)    
Type of Study: Original article | Subject: Exercise Physiology
Received: 2016/06/29 | Accepted: 2016/12/24 | Published: 2017/01/18

References
1. Dailey G. Overall mortality in diabetes mellitus: where do we stand today? Diabetes Technol Ther 2011; 13(S1): S65-74.
2. Rains JL, Jain SK. Oxidative stress, insulin signaling, and diabetes. Free Radic Biol Med 2011; 50(5): 567-75.
3. American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care 2014; 37(1): S81–90.
4. Pérez-Matute P, Zulet M, Martínez JA. Reactive species and diabetes: counteracting oxidative stress to improve health. Curr Opin Pharmacol 2009; 9(6): 771-9.
5. Porter KE, Riches K. The vascular smooth muscle cell: a therapeutic target in Type 2 diabetes? Clin Sci (Lond) 2013; 125(4): 167-82.
6. Hsu WT, Tsai LY, Lin SK, Hsiao JK, Chen BH. Effects of diabetes duration and glycemic control on free radicals in children with type 1 diabetes mellitus. Ann Clin Lab Sci 2006; 36(2): 174-8.
7. Folli F, Corradi D, Fanti P, Davalli A, Paez A, Giaccari A, et al. The role of oxidative stress in the pathogenesis of type 2 diabetes mellitus micro- and macrovascular complications: avenues for a mechanistic-based therapeutic approach. Curr Diabetes Rev 2011; 7(5): 313–24.
8. Raedschelders K, Ansley DM, Chen DD. The cellular and molecular origin of reactive oxygen species generation during myocardial ischemia and reperfusion. Pharmacol Ther 2012; 133(2): 230–55.
9. Ansley DM, Wang B. Oxidative stress and myocardial injury in the diabetic heart. J Pathol 2013; 229(2): 232-41.
11. West IC. Radicals and oxidative stress in diabetes. Diabet Med 2000; 17(3): 171-80.
12. Fisher-Wellman K, Bloomer RJ. Acute exercise and oxidative stress: a 30 year history. Dyn Med 2009; 8(1): 1-25.
14. Asmat U, Abad K, Ismail K. Diabetes mellitus and oxidative stress-A concise review. Saudi Pharm J 2016; 24(5): 547-53.
15. Tsutsui H, Kinugawa S, Matsushima S, Yokota T. Oxidative stress in cardiac and skeletal muscle dysfunction associated with diabetes mellitus. J Clin Bioche Nutr 2011; 48(1): 68-71.
16. Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circ Res 2010; 107(9):1058-70.
17. American Diabetes Association: clinical practice recommendations. Diabetes Care 1998; 21: S1-95.
18. Ascensão A, Magalhães J, Soares J, Oliveira J, Duarte JA. Exercise and cardiac oxidative stress. Rev Port Cardiol 2003; (5):651-78.
19. Atalay M, Sen CK. Physical exercise and antioxidant defenses in the heart. Ann N Y Acad Sci 1999; 874(1): 169-77.
21. Husain K, Somani SM. Response of cardiac antioxidant system to alcohol and exercise training in the rat. Alcohol 1997; 14(3): 301-07.
22. Naderi R, Mohaddes G, Mohammadi M, Ghaznavi R, Ghyasi R, Vatankhah AM. Voluntary exercise protects heart from oxidative stress in diabetic rats. Adv Pharm Bull 2015; 5(2): 231-36.
23. Judge S, Jang YM, Smith A, Selman C, Phillips T, Speakman JR, et al. Exercise by lifelong voluntary wheel running reduces subsarcolemmal and interfibrillar mitochondrial hydrogen peroxide production in the heart. Am J Physiol Regul Integr Comp Physiol 2005; 289(6): R1564-72.
24. Ascensão A, Ferreira R, Magalhães J. Exercise-induced cardioprotection - biochemical, morphological and functional evidence in whole tissue and isolated mitochondria. Int J Cardiol 2007; 117(1): 16–30.
25. King AJF. The use of animal models in diabetes research. Br J Pharmacol 2012; 166(3): 877-94.
26. Waer HF, Helmy SA. Cytological and histochemical studies in rat liver and pancreas during progression of streptozotocini nduced diabetes and possible protection of certain natural antioxidants. J Nutr Food Sci 2012; 48: 452-71.
27. Emam MA. Comparative evaluation of antidiabetic activity of Rosmarinus officinalis L. and Chamomile recutita in streptozotocin induced diabetic rats. Agr Biol J N Am 2012; 3(6): 247-52.
28. Chae CH, Jung SL, An SH, Park BY, Wang SW, Cho IH, et al. Treadmill exercise improves cognitive function and facilitates nerve growth factor signaling by activating mitogen-activated protein kinase/extracellular signal-regulated kinase1/2 in the streptozotocin-induced diabetic rat hippocampus. Neuroscience 2009; 164(4): 1665-73.
29. Aluwong T, Ayo J, Kpukple A, Oladipo OO. Amelioration of hyperglycaemia, oxidative stress and dyslipidaemia in alloxan-induced diabetic Wistar rats treated with probiotic and vitamin C. Nutrients 2016; 8(5): 151.
30. Amessou M, Bortoli S, Liemans V, Collinet M, Desbuquois B, Brichard S, et al. Treatment of streptozotocin-induced diabetic rats with vanadate and phlorizin prevents the over-expression of the liver insulin receptor gene. Eur J Endocrinol 1999; 140(1): 79-86.
31. Ali MM, El Kader MA. The influence of naringin on the oxidative state of rats with streptozotocin-induced acute hyperglycaemia. Z Naturforsch C 2004; 59(9-10): 726-33.
32. Spitz DR, Oberley LW. An assay for superoxide dismutase activity in mammalian tissue homogenates. Anal Biochem 1989; 179(1): 8-18.
33. Lawrence RA, Burk RF. Glutathione peroxidase activity in selenium-deficient rat liver. Biochem Biophys Res Commun 1976; 71(4): 952-8.
34. Aebi H. Catalase in vitro. Methods Enzymol 1984; 105: 121-26.
35. Jain SK, McVie R, Duett J, Herbst JJ. Erythrocyte membrane lipid peroxidation and glycolylated hemoglobin in diabetes. Diabetes 1989; 38(12): 1539-43.
36. Selvaraju V, Joshi M, Suresh S, Sanchez JA, Maulik N, Maulik G. Diabetes, oxidative stress, molecular mechanism, and cardiovascular disease-an overview. Toxicol Mech Methods 2012; 22(5): 330-5.
37. Wang GG, Li W, Lu XH, Zhao X, Xu L. Taurine attenuates oxidative stress and alleviates cardiac failure in type I diabetic rats. Croat Med J 2013; 54(2): 171-9.
38. Rauscher FM, Sanders RA, Watkins JB. Effects of coenzyme Q10 treatment on antioxidant pathways in normal and streptozotocin-induced diabetic rats. J Biochem Mol Toxicol 2001; 15(1): 41-6.
39. Ouali K, Trea F, Toumi ML, Bairi M, Siaud P, Guellati M. Oxidative stress in streptozotocin-induced experimental diabetes in rats is associated with changes of antioxidant status of heart tissue. Sci Technologie C 2007; 18-23.
40. Pieper GM, Jordan M, Dondlinger LA, Adams MB, Roza AM. Peroxidative stress in diabetic blood vessels. Reversal by pancreatic islet transplantation. Diabetes 1995; 44(8): 884-89.
41. Karasu C. Time course of changes in endothelium-dependent and -independent relaxation of chronically diabetic aorta: role of reactive oxygen species. Eur J Pharmacol 2000; 392(3): 163-73.
42. Laher I, Beam J, Botta A, Barendregt R, Sulistyoningrum D, Devlin A, et al. Short-term exercise worsens cardiac oxidative stress and fibrosis in 8-month-old db/db mice by depleting cardiac glutathione. Free Radic Res 2013; 47(1): 44-54.
43. Tiidus PM. Radical species in inflammation and overtraining. Can J Physiol Pharmacol 1998; 76(5): 533-38.
44. Kihlstrom M. Protection effect of endurance training against reoxygenation-induced injuries in rat heart. J Appl Physiol 1990; 68(4): 1672-78.
45. Kim JD, Yu BP, McCarter RJ, Lee SY, Herlihy JT. Exercise and diet modulate cardiac lipid peroxidation and antioxidant defenses. Free Radic Bio Med 1996; 20(1): 83-8.
46. Kutlu M, Naziroglu M, Simsek H, Yilmaz T, Sahap Kukner A. Moderate exercise combined with dietary vitamins C and E counteracts oxidative stress in the kidney and lens of streptozotocin-induced diabetic-rat. Int J Vitam Nutr Res 2005; 75(1): 71-80.

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | SSU_Journals

Designed & Developed by : Yektaweb