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钙通道参与野田癫痫大鼠海马CA3锥体细胞的异常兴奋性

Involvement of Ca(2+) channels in abnormal excitability of hippocampal CA3 pyramidal cells in noda epileptic rats.

作者信息

Kiura Yoshihiro, Hanaya Ryosuke, Serikawa Tadao, Kurisu Kaoru, Sakai Norio, Sasa Masashi

机构信息

Department of Molecular and Pharmacological Neuroscience, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

出版信息

J Pharmacol Sci. 2003 Feb;91(2):137-44. doi: 10.1254/jphs.91.137.

DOI:10.1254/jphs.91.137
PMID:12686757
Abstract

Noda epileptic rat (NER) is a mutant rat, which spontaneously exhibits a tonic-clonic convulsion from 14 weeks of age. An intracellular recording study was performed to elucidate the abnormal excitability of NER hippocampal CA3 neurons. The recorded neurons were classified into two groups, group A and B neurons, according to the responses to a single stimulation of mossy fibers. In group A neurons, a stimulus elicited a long-lasting depolarization shift accompanying repetitive firings followed by after-hyperpolarization. In group B neurons, the same stimulus elicited a single spike without a long-lasting depolarization shift. Bath application of 1 mM Cd(2+), a nonselective Ca(2+) channel blocker, completely inhibited the abnormal excitation in group A neurons. We further examined the character of Ca(2+) spikes in NER CA3 neurons. Ca(2+) spikes were completely blocked by 10 microM Cd(2+) in group A neurons, but not in either group B or control neurons, suggesting that Ca(2+) channels in NER group A neurons have the hypersensitivity to Cd(2+). Analysis using subtype specific blockers of Ca(2+) channel raised the possible involvement of T-type Ca(2+) channels. These results suggest that Ca(2+) channel dysfunction is involved in the abnormal excitability of CA3 pyramidal neurons and pathogenesis of epilepsy in NER.

摘要

野田癫痫大鼠(NER)是一种突变大鼠,从14周龄起会自发出现强直阵挛性惊厥。进行了一项细胞内记录研究,以阐明NER海马CA3神经元的异常兴奋性。根据对苔藓纤维单次刺激的反应,将记录的神经元分为两组,即A组和B组神经元。在A组神经元中,刺激引发了伴随重复放电的持久去极化偏移,随后是超极化后电位。在B组神经元中,相同的刺激引发了单个动作电位,没有持久的去极化偏移。浴加1 mM Cd(2+)(一种非选择性Ca(2+)通道阻滞剂)完全抑制了A组神经元中的异常兴奋。我们进一步研究了NER CA3神经元中Ca(2+)动作电位的特征。10 microM Cd(2+)完全阻断了A组神经元中的Ca(2+)动作电位,但对B组神经元或对照神经元均无影响,这表明NER A组神经元中的Ca(2+)通道对Cd(2+)具有超敏感性。使用Ca(2+)通道亚型特异性阻滞剂进行的分析提示T型Ca(2+)通道可能参与其中。这些结果表明,Ca(2+)通道功能障碍与CA3锥体神经元的异常兴奋性及NER癫痫的发病机制有关。

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