Presynaptic excitability as a potential target for the treatment of the traumatic cerebellum

被引:10
作者
Ai, JL [1 ]
Baker, A [1 ]
机构
[1] Univ Toronto, St Michaels Hosp, Cara Phelan Ctr Trauma Res, Traumat Brain Injury Lab, Toronto, ON M5B 1W8, Canada
关键词
cerebellum; neurotransmission; presynaptic excitability; traumatic brain injury; experimental treatment; traumatic cerebellum; Purkinje cell death;
D O I
10.1159/000078085
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Using an extracellular recording method, we have previously shown a hyperexcitability of the presynaptic response in fluid percussion injury (FPI) in rats. In this study, we demonstrated that treatment with cis-ACBD, a glutamate reuptake inhibitor, depressed the presynaptic potential (PSP) in naive/sham controls, while it potentiated the PSP in FPI rats. On the contrary, (RS)-APICA, a selective group II metabotropic glutamate receptor antagonist, potentiated PSP in controls, but depressed PSP in FPI rats. These results indicate that an alteration of the normal function of metabotropic glutamate receptors and glutamate reuptake system or an altered reactivity of presynaptic fibers was induced by FPI. This alteration may contribute to the reported loss of Purkinje cells after FPI. PSP may be used as a potential tool for evaluating treatments of FPI or as a potential target for the prevention of Purkinje cell death. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:192 / 198
页数:7
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