## Abstract In view of the antioxidant properties of melatonin, the effects of melatonin on the oxidative–antioxidative status of tissues affected by diabetes, e.g. liver, heart and kidneys, were investigated in streptozotocin (STZ)‐induced diabetic rats in the present study. Concentrations of malo
Effect of cobalt on the oxidative status in heart and aorta of streptozotocin-induced diabetic rats
✍ Scribed by Özlem Yildirim; Zeliha Büyükbingöl
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 180 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0263-6484
- DOI
- 10.1002/cbf.995
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✦ Synopsis
Abstract
Effects of cobalt on the antioxidant status of control and streptozotocin diabetic rat heart and aorta were examined at the second, fourth and sixth week of treatment. Rats were divided into four groups: control, diabetic, control treated with cobalt chloride and diabetic treated with cobalt chloride. Diabetes was induced by tail vein injection of streptozotocin (STZ). Cobalt treatment groups were given 0.5 mM of CoCl~2~ in drinking water. The rats in both groups were further subdivided into three groups of six rats each. Rats in these subgroups were studied at 2‐week intervals up to 6 weeks. At the end of the experiment, all animals were sacrified by decapitation, heart and aorta samples were removed for determination of thiobarbituric acid reactive substance (TBARS) level and superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH‐Px) activities. It was found that lipid peroxidation levels and antioxidant enzyme activities were increased in the streptozotocin‐induced diabetic rats at all times studied. Cobalt treatment of diabetic rats (0.5 mM in drinking water) resulted in attenuation of the increased levels of TBARS and antioxidant enzyme activities in heart and aorta. Thus, the effect of oral administration of cobalt at this dose during the early stage of experimental diabetes can be considered as a consequence of altered endogenous defence mechanisms in heart and aorta. Copyright © 2002 John Wiley & Sons, Ltd.
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