Chromium picolinate attenuates hyperglycemia-induced oxidative stress in streptozotocin-induced diabetic rats

被引:39
作者
Sundaram, Bhuvaneshwari [1 ]
Aggarwal, Aanchal [1 ]
Sandhir, Rajat [1 ]
机构
[1] Panjab Univ, Dept Biochem, Chandigarh 160014, India
关键词
Antioxidants; Chromium picolinate; Hyperglycemia; Oxidative stress; Liver; NF-KAPPA-B; LIPID-PEROXIDATION; INSULIN-RESISTANCE; DINICOCYSTEINATE SUPPLEMENTATION; GLUTATHIONE-REDUCTASE; SUPEROXIDE-DISMUTASE; TRIVALENT CHROMIUM; ANTIOXIDANT STATUS; VITAMIN-C; MELLITUS;
D O I
10.1016/j.jtemb.2012.09.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chromium picolinate is advocated as an anti-diabetic agent for impaired glycemic control. It is a transition metal that exists in various oxidation states and may thereby act as a pro-oxidant. The present study has been designed to examine the effect of chromium picolinate supplementation on hyperglycemia-induced oxidative stress: Diabetes was induced in male Wistar rats by a single intraperitoneal injection of streptozotocin (50 mg/kg body weight) and chromium was administered orally as chromium picolinate (1 mg/kg body weight) daily for a period of four weeks after the induction of diabetes. As is characteristic of diabetic condition, hyperglycemia was associated with an increase in oxidative stress in liver in terms of increased lipid peroxidation and decreased glutathione levels. The activity of antioxidant enzymes like superoxide dismutase, catalase and glutathione reductase were significantly reduced in liver of diabetic animals. Levels of alpha-tocopherol and ascorbic acid were found to be considerably lower in plasma of diabetic rats. Chromium picolinate administration on the other hand was found to have beneficial effect in normalizing glucose levels, lipid peroxidation and antioxidant status. The results from the present study demonstrate potential of chromium picolinate to attenuate hyperglycemia-induced oxidative stress in experimental diabetes. (C) 2012 Elsevier GmbH. All rights reserved.
引用
收藏
页码:117 / 121
页数:5
相关论文
共 55 条
[1]   Chromium supplementation improves glucose tolerance in diabetic Goto-Kakizaki rats [J].
Abdourahman, Aicha ;
Edwards, John G. .
IUBMB LIFE, 2008, 60 (08) :541-548
[2]  
Anderson RA, 2000, DIABETES METAB, V26, P22
[3]   Chromium, glucose intolerance and diabetes [J].
Anderson, RA .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 1998, 17 (06) :548-555
[4]   Elevated intakes of supplemental chromium improve glucose and insulin variables in individuals with type 2 diabetes [J].
Anderson, RA ;
Cheng, NZ ;
Bryden, NA ;
Polansky, MM ;
Cheng, NP ;
Chi, JM ;
Feng, JG .
DIABETES, 1997, 46 (11) :1786-1791
[5]   Potential antioxidant effects of zinc and chromium supplementation in people with type 2 diabetes mellitus [J].
Anderson, RA ;
Roussel, AM ;
Zouari, N ;
Mahjoub, S ;
Matheau, JM ;
Kerkeni, A .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2001, 20 (03) :212-218
[6]   NONALCOHOLIC FATTY LIVER DISEASE Liver disease: an overlooked complication of diabetes mellitus [J].
Arrese, Marco .
NATURE REVIEWS ENDOCRINOLOGY, 2010, 6 (12) :660-661
[7]   Cytotoxicity and oxidative mechanisms of different forms of chromium [J].
Bagchi, D ;
Stohs, SJ ;
Downs, BW ;
Bagchi, M ;
Preuss, HG .
TOXICOLOGY, 2002, 180 (01) :5-22
[8]   Determining the safety of chromium tripicolinate for addition to foods as a nutrient supplement [J].
Berner, TO ;
Murphy, MM ;
Slesinski, R .
FOOD AND CHEMICAL TOXICOLOGY, 2004, 42 (06) :1029-1042
[9]   ERYTHROCYTE GLUTATHIONE REDUCTASE [J].
BEUTLER, E ;
YEH, MKY .
BLOOD, 1963, 21 (05) :573-&
[10]  
BRADLEY DW, 1972, CLIN CHEM, V18, P1442