Mitochondrial oxidative stress after global brain ischemia in rats

被引:60
作者
Friberg, H
Wieloch, T
Castilho, RF
机构
[1] Lund Univ, Wallenberg Neurosci Ctr, Expt Brain Res Lab, S-22362 Lund, Sweden
[2] Lund Univ Hosp, Dept Anesthesiol & Intens Care, S-22185 Lund, Sweden
[3] Univ Estadual Campinas, Sch Med Sci, Dept Clin Pathol, BR-13083970 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
brain; calcium; cyclosporin A; free radicals; ischemia; mitochondria; permeability transition;
D O I
10.1016/S0304-3940(02)01116-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Vulnerable neurons in the hippocampus die 2-3 days after transient global brain ischemia. In the present study, rat brain mitochondria were isolated at different time points (4 h, 24 h and 48 h) after transient global ischemia. Detection of mitochondrially-generated reactive oxygen species, measured through dichlorodihydrofluorescein oxidation, was increased up to 40% relative to control in hippocampal mitochondria at 4 h and 48 h of reperfusion. Ischemia-stimulated oxidative stress was observed with mitochondria oxidizing substrates linked to nicotinamide adenine dinucleotide or flavin adenine dinucleotide, but not in the presence of the respiratory chain inhibitor antimycin A. A slightly decreased Ca2+ uptake capacity was observed in hippocampal mitochondria during reperfusion. We conclude that transient brain ischemia induces oxidative stress in hippocampal mitochondria. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:111 / 114
页数:4
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