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通过脑室内注射钙通道激动剂BAY k 8644在小鼠中诱发癫痫发作。

Induction of seizures in mice by intracerebroventricular administration of the calcium channel agonist BAY k 8644.

作者信息

Shelton R C, Grebb J A, Freed W J

出版信息

Brain Res. 1987 Feb 3;402(2):399-402. doi: 10.1016/0006-8993(87)90054-0.

Abstract

The calcium channel agonist BAY k 8644 was used to investigate the role of the calcium ion (Ca2+) in epileptogenesis. Intracerebroventricular administration of the compound induced murine seizures that were reversed by calcium channel inhibitors (CCIs) but not by anticonvulsants such as carbamazepine, pentobarbital, and diazepam. The seizures were exacerbated by phenytoin and valproic acid. Chronic administration of CCI's, previously shown to produce down-regulation of the binding of the CCI [3H]nitrendipine, resulted in augmentation of BAY k 8644-induced seizures.

摘要

钙通道激动剂BAY k 8644被用于研究钙离子(Ca2+)在癫痫发生中的作用。向脑室内注射该化合物可诱发小鼠癫痫发作,钙通道抑制剂(CCIs)可逆转这种发作,但抗惊厥药如卡马西平、戊巴比妥和地西泮则不能。苯妥英和丙戊酸会加剧癫痫发作。先前的研究表明,长期给予CCIs会导致CCI [3H]尼群地平结合下调,结果BAY k 8644诱发的癫痫发作增强。

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