Low-carbohydrate diet and oxidative stress in diabetic and nondiabetic rats
Hyperglycemia of diabetes has been implicated in increased tissue oxidative stress, with consequent development of secondary complications. Thus, stabilizing glucose levels near normal levels is of utmost importance. Because diet influences glycemic control, this study investigated whether a low‐car...
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Veröffentlicht in: | Journal of biochemical and molecular toxicology 2006-01, Vol.20 (5), p.259-269 |
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Sprache: | eng |
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Zusammenfassung: | Hyperglycemia of diabetes has been implicated in increased tissue oxidative stress, with consequent development of secondary complications. Thus, stabilizing glucose levels near normal levels is of utmost importance. Because diet influences glycemic control, this study investigated whether a low‐carbohydrate (5.5%) diet confers beneficial effects on the oxidative status of the heart, kidney, and liver in diabetes. Male and female normal and diabetic rats were fed standard chow (63% carbohydrates) or low‐carbohydrate diet for 30 days. Elevated glucose, HbA1c, and alanine and aspartate aminotransferases in diabetic animals were reduced or normalized by the low‐carbohydrate diet. While diabetes increased cardiac activities of glutathione peroxidase and catalase, low‐carbohydrate diet normalized cardiac glutathione peroxidase activity in diabetic animals, and reduced catalase activity in females. Diabetic rats fed low‐carbohydrate diet had altered activities of renal glutathione reductase and superoxide dismutase, but increased renal glutathione peroxidase activity in diabetic animals was not corrected by the test diet. In the liver, diabetes was associated with a decrease in catalase activity and glutathione levels and an increase in glutathione peroxidase and γ‐glutamyltranspeptidase activities. Decreased hepatic glutathione peroxidase activity and lipid peroxidation were noted in diet‐treated diabetic rats. Overall, the low‐carbohydrate diet helped stabilize hyperglycemia and did not produce overtly negative effects in tissues of normal or diabetic rats. © 2006 Wiley Periodicals, Inc. J Biochem Mol Toxicol 20:259–269, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.20142 |
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ISSN: | 1095-6670 1099-0461 |
DOI: | 10.1002/jbt.20142 |