Caspase-3-dependent neuronal death in the hippocampus following kainic acid treatment

被引:96
作者
Faherty, CJ
Xanthoudakis, S
Smeyne, RJ
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
[2] Merck Frosst Ctr Therapeut Res, Dept Biochem & Mol Biol, Kirkland, PQ, Canada
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 70卷 / 01期
关键词
seizure; strain; apoptosis; TUNEL; excitotoxicity;
D O I
10.1016/S0169-328X(99)00143-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In this study, we examined the levels of activated caspase-3 in the kainic acid (KA) model of hippocampal degeneration in both sensitive (FVB/N) and resistant (129/SvEMS) strains of mice. At 30 h, 2 and 4 days following KA administration, animals were sacrificed and brains examined for pyknosis, TUNEL labeling, and activated caspase-3 immunoreactivity. Catalytically active caspase-3 was first detected 30 h following KA treatment in the sensitive, FVB/N strain. This was 18 h before the appearance of pyknosis or TUNEL labeling. The expression of activated caspase-3 continues up to 4 days post-injection. No activated caspase-3 immunoreactivity was detected in the resistant, 129/SvEMS strain, neither was there evidence of pyknosis or TUNEL staining. This suggests that activation of caspase-3 is a necessary component of KA-induced cell death. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:159 / 163
页数:5
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