Combined Effect of Swimming Training and Arbutin Supplementation on Kidney Total Oxidant and Antioxidant Status in Alloxan-induced Diabetic Rats

Authors
1 Department of Exercise Physiology, Faculty of Humanities, Sari Branch, Islamic Azad University, Sari, Iran
2 Department of Exercise Physiology, Ghaemshahr Branch, Islamic Azad University, Ghaemshahr, Iran
Abstract
Objective: Diabetes is a common metabolic disorder that a one of the important factors in the etiology is considered to oxidative damage. The present study intends to study the effect of swimming training with Arbutin on total oxidant status (TOS) and total antioxidant status (TAS) in kidney tissue of Alloxan-induced diabetic rats.
Methods: We randomly divided 42 male Wistar rats that had an average weight of 195 g to 220 g into 6 groups (7 rats per group) - control, diabetic, arbutin, diabetic-arbutin, diabetic-swimming training, and diabetic-combinatorial. Swimming training protocol consisted of 5 days/week for 6 weeks at 5-36 min/day. Diabetes was induced with alloxan [90 mg/kg, intraperitoneal (ip)] in the rats. Arbutin (50 mg/kg, subcutaneous) was administered for 5 days/week. The rats were killed 48 hours after the last treatments and kidney TOS and TAS levels were evaluated. One-way analysis of variance was used for data analysis.
Results: After six weeks of supplementation with arbutin, swimming training and the combination of swimming training and arbutin, we observed a significant decrease in TOS (P<0.05) and elevated TAS (P<0.05) levels in the alloxan-induced diabetic rats.
Conclusion: The combined effect of swimming training and arbutin supplementation can play a major role against renal oxidative stress by modulating total oxidant and antioxidant status in alloxan-induced diabetic rats.

Keywords


[1]     Zhang X, Chen C. A new insight of mechanisms, diagnosis and treatment of diabetic cardiomyopathy. Endocrine 2012; 41(3): 398-409.
[2]     Tripathi BK, Srivastava AK. Diabetes mellitus: complications and therapeutics. Med Sci Monit 2006; 12(7): R130-47.
[3]     Esteghamati AR, Zarban A, Doosti M. Evaulation of antioxidant status and oxidative stress markers in type II Diabetes mellitus. Iranian Journal of Endocrinology and Metabolism 2001; 3 (4) :239-45.
[4]     Baynes JW. Role of oxidative stress in development of complications in diabetes. Diabetes 1991; 40(4): 405-12.
[5]     Ohkubo Y, Kishikawa H, Araki E, Miyata T, Isami S, Motoyoshi S, Kojima Y, Furuyoshi N, Shichiri M. Intensive insulin therapy prevents the progression of diabetic microvascular complications in Japanese patients with non-insulin-dependent diabetes mellitus: a randomized prospective 6-year study. Diabetes Res Clin Pract 1995; 28(2): 103-17.
[6]     Baynes JW. Role of oxidative stress in development of complications in diabetes. Diabetes 1991; 40(4): 405-12.
[7]     Radak Z. Free radicals in exercise and aging. 1st edition, Budapest, Hungary: Human Kinetics, 2000.
[8]     Zanburi V, Kalantari S, Sharifi F. The effects of triple-therapy in metabolic control of patients suffering from type 2 diabetic mellitus (DM). ZUMS Journal 2007; 15(60): 17-26.
[9]     Ozbek E. Induction of oxidative stress in kidney. Int J Nephrol 2012; 2012: 465897
[10] Forbes JM, Coughlan MT, Cooper ME. Oxidative stress as a major culprit in kidney disease in diabetes. Diabetes 2008; 57(6): 1446-54.
[11] Signorini AM, Fondelli C, Renzoni E, Puccetti C, Gragnoli G, Giorgi G. Antioxidant effect of gliclazide, glibenclamide and metformin in patients with type 2 diabetes mellitus. Current Therapeutic Research 2002; 63(7): 411-20.
[12] Sen CK, Rankinen T, Väisänen S, Rauramaa R. Oxidative stress after human exercise: effect of N-acetylcysteine supplementation. J Appl Physiol (1985) 1994; 76(6): 2570-7.
[13] Jakus V. The role of free radicals, oxidative stress and antioxidant systems in diabetic vascular disease. Bratisl Lek Listy 2000; 101(10): 541-51.
[14] van Dam PS, Bravenboer B, van Asbeck BS, van Oirschot JF, Marx JJ, Gispen WH. Effects of insulin treatment on endoneurial and systemic oxidative stress in relation to nerve conduction in streptozotocin-diabetic rats. Eur J Clin Invest 1996; 26(12): 1143-9.
[15] Aksoy L, Kolay E, Ağılönü Y, Aslan Z, Kargıoğlu M. Free radical scavenging activity, total phenolic content, total antioxidant status, and total oxidant status of endemic Thermopsis turcica. Saudi J Biol Sci 2013; 20(3): 235-9.
[16] Wei D, Zhang XL, Wang YZ, Yang CX, Chen G. Lipid peroxidation levels, total oxidant status and superoxide dismutase in serum, saliva and gingival crevicular fluid in chronic periodontitis patients before and after periodontal therapy. Aust Dent J 2010;55(1):70-8.
[17] Lovasova E , Sesztakova E. Total antioxidant status – a possible marker of environmental influences on animal organisms. Slovak J Anim Sci 2009; 42(Suppl 1): 42-5.
[18] Gul A, Rahman MA. Antioxidant status in diabetic and non-diabetic senile patients, with cataract or cardiovascular complications. Saudi Med J 2008; 29(2): 179-84.
[19] Dosoo DK, Rana SV, Offe-Amoyaw K, Tete-Donkor D, Maddy SQ. Total antioxidant status in non-insulin-dependent diabetes mellitus patients in Ghana. West Afr J Med 2001; 20(3): 184-6.
[20] Valabhji J, McColl AJ, Richmond W, Schachter M, Rubens MB, Elkeles RS. Total antioxidant status and coronary artery calcification in type 1 diabetes. Diabetes Care 2001; 24(9): 1608-13.
[21] Packer L, Rosen P, Tritschler HJ, King GL, Azzi A. Oxidative stress and antioxidants: The antioxidant network, α-lipoic acid and diabetes. In: Packer L. Antioxidants in diabetes management. 1st ed. Basel, Switzerland: Marcel Dekker Inc 2000; p: 1-15.
[22] Habibian M, Farzanegi P, Azimi G. Therapeutic effect of swimming training and arbutin supplement on diabetes-induced renal oxidative stress. Daneshvar (Medicine) Shahed University 2014; 22(114): 13-21. (Persian)
[23] Cao G, Booth SL, Sadowski JA, Prior RL. Increases in human plasma antioxidant capacity after consumption of controlled diets high in fruit and vegetables. Am J Clin Nutr 1998; 68(5): 1081-7.
[24] Cao G, Russell RM, Lischner N, Prior RL. Serum antioxidant capacity is increased by consumption of strawberries, spinach, red wine or vitamin C in elderly women. J Nutr 1998; 128(12): 2383-90.
[25] Kulisic T, Radonic A, Katalinic V, Milosa M. Use of different methods for testing antioxidative activity of oregano essential oil. Food Chemistry 2004; 85: 633-40.
[26] Ioku K, Terao J, Nakatani N. Antioxidative Activity of Arbutin in a Solution and Liposomal Suspension. Biosci Biotech Biochem 1992; 56(10): 1658-9.
[27] Ramprasath T, Kumar PH, Puhari SS, Murugan PS, Vasudevan V, Selvam GS. L-Arginine ameliorates cardiac left ventricular oxidative stress by upregulating eNOS and Nrf2 target genes in alloxan-induced hyperglycemic rats. Biochem Biophys Res Commun 2012; 428(3): 389-94
[28] Matsuda H, Nakata H, Tanaka T, Kubo M. Pharmacological study on Arctostaphylos uva-ursi (L.) Spreng. II. Combined effects of arbutin and prednisolone or dexamethazone on immuno-inflammation. Yakugaku Zasshi 1990; 110(1): 68-76.
[29] Lunz W, Peluzio MC, Dias CM, Moreira AP, Natali AJ. Long-term aerobic swimming training by rats reduces the number of aberrant crypt foci in 1,2-dimethylhydrazine-induced colon cancer. Braz J Med Biol Res 2008; 41(11): 1000-4.
[30] Monazzami A, Rajabi H, Omidfar K, Mostafaie A. Endurance training increases skeletal muscle NA/H+ exchanger1 (NHE1) and NA/HCO3 co-transporter1 (NBC1) gene expressions in type2 diabetic rat. Iranian Journal of Diabetes and Metabolism 2014; 13(5): 400-12. (Persian)
[31] Cesur G, Atay E, Ogut S, Polat M, Ongel K. Effect of indoor climbing exercise on plasma oxidative stress, hematologic parameters and heart rate responses in sedentary individuals. Biomed Res- India 2012; 23(4): 566-70.
[32] Memisoğullari R, Taysi S, Bakan E, Capoglu I. Antioxidant status and lipid peroxidation in type II diabetes mellitus. Cell Biochem Funct 2003; 21(3): 291-6.
[33] Keshari KR, Wilson DM, Sai V, Bok R, Jen KY, Larson P, Van Criekinge M, Kurhanewicz J, Wang ZJ. Noninvasive in vivo imaging of diabetes-induced renal oxidative stress and response to therapy using hyperpolarized 13C dehydroascorbate magnetic resonance. Diabetes 2015; 64(2): 344-52.
[34] Çelık VK, Şahın ZD, Sari İ, Bakir S. Comparison of oxidant/antioxidant, detoxification systems in various tissue homogenates and mitochondria of rats with diabetes induced by streptozocin. Exp Diabetes Res 2012; 2012: 386831.
[35] Verma AK, Chandra S, Singh RG, Singh TB, Srivastava S, Srivastava R. Serum prolidase activity and oxidative stress in diabetic nephropathy and end stage renal disease: a correlative study with glucose and creatinine. Biochem Res Int 2014; 2014: 291458.
[36] Odum EP, Ejilemele AA, Wakwe VC. Antioxidant status of type 2 diabetic patients in Port Harcourt, Nigeria. Niger J Clin Pract 2012; 15(1): 55-8.
[37] Vincent AM, Russell JW, Low P, Feldman EL. Oxidative stress in the pathogenesis of diabetic neuropathy. Endocr Rev 2004; 25(4): 612-28.
[38] Kusano C, Ferrari B. Total antioxidant capacity: a biomarker in biomedical and nutritional studies. J Cell Mol Biol 2008; 7: 1-5.
[39] Ghosh S, Khazaei M, Moien-Afshari F, Ang LS, Granville DJ, Verchere CB, Dunn SR, McCue P, Mizisin A, Sharma K, Laher I. Moderate exercise attenuates caspase-3 activity, oxidative stress, and inhibits progression of diabetic renal disease in db/db mice. Am J Physiol Renal Physiol 2009; 296(4): F700-8.
[40] Ishikawa Y, Gohda T, Tanimoto M, Omote K, Furukawa M, Yamaguchi S, Murakoshi M, Hagiwara S, Horikoshi S, Funabiki K, Tomino Y. Effect of exercise on kidney function, oxidative stress, and inflammation in type 2 diabetic KK-A(y) Mice. Exp Diabetes Res 2012; 2012: 702948.
[41] Farzanegi P, Saberi S, Fakharian A, Rasaee MJ, Dabidi Roshan V. Combined Effects of Curcuma longa and Exercise Training on Kidney and Spleen Tissue Levels of Glutathione Peroxidase and Protein Carbonyl in Rats Exposed to Lead. Modares Journal of Medical Sciences: Pathobiology 2012; 15(3): 49-62.
[42] Boor P, Celec P, Behuliak M, Grancic P, Kebis A, Kukan M, Pronayová N, Liptaj T, Ostendorf T, Sebeková K. Regular moderate exercise reduces advanced glycation and ameliorates early diabetic nephropathy in obese Zucker rats. Metabolism 2009; 58(11): 1669-77.
[43] Pal PB, Sinha K1, Sil PC1. Mangiferin attenuates diabetic nephropathy by inhibiting oxidative stress mediated signaling cascade, TNFα related and mitochondrial dependent apoptotic pathways in streptozotocin-induced diabetic rats. PLoS One 2014; 9(9): e107220.
[44] Mohandas R, Paramesha S, Suchetha Kumari N, Damodara Gowda KM, VidhyaGG. Effect of garlic on total antioxidants in alloxan induced diabetes rats. IJBAR 2011; 2(9): 317-28.
[45] Trujillo J, Chirino YI, Molina-Jijón E, Andérica-Romero AC, Tapia E, Pedraza-Chaverrí J. Renoprotective effect of the antioxidant curcumin: Recent findings. Redox Biol 2013; 1: 448-56.
[46] Farzanegi P, Mousavi M, Ghanbari-Niaki A. Effect of Pistacia atlantica extract on glutathione peroxidase tissue levels and total oxidative capacity of liver and plasma lipid profile of rats. ZJRMS 2013; 15(11): 59-63.