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首页> 外文期刊>Journal of pharmacological sciences. >Involvement of Ca2+ Channels in Abnormal Excitability of Hippocampal CA3 Pyramidal Cells in Noda Epileptic Rats
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Involvement of Ca2+ Channels in Abnormal Excitability of Hippocampal CA3 Pyramidal Cells in Noda Epileptic Rats

机译:Ca2 +通道参与野田癫痫大鼠海马CA3锥体细胞异常兴奋性。

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References(21) Cited-By(7) 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 Cd2+, a nonselective Ca2+ channel blocker, completely inhibited the abnormal excitation in group A neurons. We further examined the character of Ca2+ spikes in NER CA3 neurons. Ca2+ spikes were completely blocked by 10 μM Cd2+ in group A neurons, but not in either group B or control neurons, suggesting that Ca2+ channels in NER group A neurons have the hypersensitivity to Cd2+. Analysis using subtype specific blockers of Ca2+ channel raised the possible involvement of T-type Ca2+ channels. These results suggest that Ca2+ channel dysfunction is involved in the abnormal excitability of CA3 pyramidal neurons and pathogenesis of epilepsy in NER.
机译:参考文献(21)被引用的By(7)Noda癫痫大鼠(NER)是突变的大鼠,自14周龄起自然表现出强直-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。根据对苔藓纤维的单次刺激的响应,记录的神经元分为A组和B组两个神经元。在A组神经元中,刺激会引起持续的去极化转变,伴随着反复的放电和随后的超极化。在B组神经元中,相同的刺激引起单个尖峰,而没有持久的去极化移位。浴液中使用1 mM Cd2 +(一种非选择性的Ca2 +通道阻滞剂)完全抑制了A组神经元的异常兴奋。我们进一步检查了NER CA3神经元中Ca2 +尖峰的特征。在A组神经元中,Ca2 +峰被10μMCd2 +完全阻断,但在B组或对照神经元中均没有,这表明NER A组神经元中的Ca2 +通道对Cd2 +过敏。使用亚型特异性Ca2 +通道阻滞剂的分析提出了T型Ca2 +通道的可能参与。这些结果表明,Ca2 +通道功能异常与NER的CA3锥体神经元异常兴奋性和癫痫的发病机理有关。

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