LUTEIN AND DOCOSAHEXAENOIC ACID PREVENT CORTEX LIPID PEROXIDATION IN STREPTOZOTOCIN-INDUCED DIABETIC RAT CEREBRAL CORTEX

被引:51
作者
Arnal, E. [2 ]
Miranda, M. [1 ]
Barcia, J. [1 ]
Bosch-Morell, F. [1 ,2 ]
Romero, F. J. [1 ,2 ]
机构
[1] Univ Cardenal Herrera, Dept Fisiol Farmacol & Toxicol, Valencia 46113, Spain
[2] Fdn Oftalmol Mediterraneo, Valencia, Spain
关键词
lutein; docosahexaenoic acid; cortex; 4-hydroxynonenal; malondialdehyde; glutathione; N-3; FATTY-ACIDS; OXIDATIVE STRESS; VITAMIN-E; ALDEHYDIC PRODUCT; ION HOMEOSTASIS; GLUTATHIONE; BRAIN; HIPPOCAMPAL; MALONDIALDEHYDE; PERFORMANCE;
D O I
10.1016/j.neuroscience.2009.12.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mechanisms underlying diabetic encephalopathy, are largely unknown. Here, we examined whether docosahexaenoic acid (DHA) and lutein could attenuate the oxidative changes of the diabetic cerebral cortex. The levels of malondialdehyde (MDA) were significantly increased and glutathione (GSH) and glutathione peroxidase activity (GPx) were decreased in diabetic rats. The number of 4-hydroxynonenal (4-HNE) positive cells was increased. Treatment with insulin, lutein or DHA and the combination of each antioxidant with insulin, significantly restored all markers concentrations mentioned above, and the increase in 4-HNE inmunofluorescence. We combined 4-HNE immunofluorescence with NeuN (Neuronal Nuclei) staining. The latter demonstrated extensive overlap with the 4-HNE staining in the cortex from diabetic rats. Our findings demonstrate a clear participation of glucose-induced oxidative stress in the diabetic encephalopathy, and that the cells suffering oxidative stress are neurons. Lowering oxidative stress through the administration of different antioxidants may be beneficial for the central nervous tissue in diabetes. (C) 2010 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:271 / 278
页数:8
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