Minocycline blocks 6-hydroxydopamine-induced neurotoxicity and free radical production in rat cerebellar granule neurons

被引:60
|
作者
Lin, SZ
Wei, X
Xu, Y
Yan, C
Dodel, R
Zhang, YQ
Liu, JY
Klaunig, JE
Farlow, M
Du, YS
机构
[1] Indiana Univ, Sch Med, Dept Neurol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
[3] Univ Bonn, Dept Neurol, D-5300 Bonn, Germany
[4] Peking Univ, Sch Pharmaceut Educ, Beijing 100871, Peoples R China
关键词
minocycline; cerebellar granule neurons; 6-ODHA; free radicals; neurotoxicity;
D O I
10.1016/S0024-3205(02)02442-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Neurotoxicity induced by 6-hydroxydopamine (6-OHDA) is believed to be due, in part, to the production of reactive oxygen species (ROS). Anti-oxidants by inhibiting free radical generation, protect neurons against 6-OHDA-induced neurotoxicity. In this study, we investigated whether or not minocycline, a neuroprotective compound, could directly protect neurons against 6-OHDA-induced neurotoxicity and inhibit 6-OHDA-induced free radical production in cultured rat cerebellar granule neurons (CGN). We now report that exposure of CGN to 6-OHDA (100 muM) resulted in a significant increase in free radical production with death of 86% of CGN. Pretreatment with minocycline (10 muM) for 2 h prevented 6-OHDA-induced free radical generation and neurotoxicity. Furthermore, minocycline also attenuated H2O2-induced neurotoxicity. Our results suggest that minocycline blocks 6-ORDA-induced neuronal death possibly by inhibiting 6-OHDA-induced free radical generation in CGN. Both the antioxidative and neuroprotective effects of minocycline may be beneficial in the therapy of Parkinson's disease and other neurodegenerative diseases. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1635 / 1641
页数:7
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