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豚鼠海马CA1神经元中1,4 - 二氢吡啶与体细胞钙电流的相互作用(体外研究)

Interaction of 1,4-dihydropyridines with somatic Ca currents in hippocampal CA1 neurones of the guinea pig in vitro.

作者信息

Docherty R J, Brown D A

出版信息

Neurosci Lett. 1986 Sep 25;70(1):110-5. doi: 10.1016/0304-3940(86)90447-7.

Abstract

Two distinct Ca currents may be recorded from guinea pig hippocampal CA1 neuronal somata: a non-inactivating (persistent) current and a rapidly inactivating (transient) current. Nimodipine, a 'calcium antagonist', reduced both Ca currents though the transient current was somewhat less sensitive than the persistent current. BAY K 8644, a 'calcium agonist' enhanced the persistent current and shifted the activation threshold for this current to more negative potentials. BAY K 8644 also enhanced the transient Ca current though the effect was very variable. The results demonstrate that Ca channels in hippocampal CA1 neurones possess a dihydropyridine receptor in common with Ca channels in other tissues.

摘要

从豚鼠海马CA1神经元胞体可记录到两种不同的钙电流:一种非失活(持续)电流和一种快速失活(瞬态)电流。“钙拮抗剂”尼莫地平降低了两种钙电流,不过瞬态电流比持续电流的敏感性略低。“钙激动剂”BAY K 8644增强了持续电流,并将该电流的激活阈值移向更负的电位。BAY K 8644也增强了瞬态钙电流,不过其效果变化很大。结果表明,海马CA1神经元中的钙通道与其他组织中的钙通道一样,都具有二氢吡啶受体。

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