AMINOOXYACETIC ACID STRIATAL LESIONS ATTENUATED BY 1,3-BUTANEDIOL AND COENZYME Q(10)

被引:20
作者
BROUILLET, E
HENSHAW, DR
SCHULZ, JB
BEAL, MF
机构
[1] MASSACHUSETTS GEN HOSP,NEUROL SERV,NEUROCHEM LAB,BOSTON,MA 02114
[2] HARVARD UNIV,SCH MED,BOSTON,MA
关键词
MITOCHONDRION; UBIQUINONE; EXCITOTOXICITY; HYPOGLYCEMIA;
D O I
10.1016/0304-3940(94)90044-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We previously showed that intrastriatal administration of aminooxyacetic acid (AOAA) produces striatal lesions by a secondary excitotoxic mechanism associated with impairment of oxidative phosphorylation. In the present study, we show that and the specific complex I inhibitor rotenone produces a similar neurochemical profile in the striatum, consistent with an effect of AOAA on energy metabolism. Lesions produced by AOAA were dose-dependently blocked by MK-801, with complete protection against GABA and substance P depletions at a dose of 3 mg/kg. AOAA lesions were significantly attenuated by pretreatment with either 1,3-butanediol or coenzyme Q(10), two compounds which are thought to improve energy metabolism. These results provide further evidence that AOAA produces striatal excitotoxic lesions as a consequence of energy depletion and they suggest therapeutic strategies which may be useful in neurodegenerative diseases.
引用
收藏
页码:58 / 62
页数:5
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