[代谢性谷氨酸受体作为抗癫痫治疗的可能靶点]。

Ceskoslovenska fysiologie Pub Date : 2007-01-01
D Lojková, P Mares
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引用次数: 0

摘要

谷氨酸嗜离子受体拮抗剂具有显著的抗惊厥作用,但也有严重的副作用,因此人们将注意力转移到影响代谢性谷氨酸受体的药物上。这些受体可分为三组(I-III)和八个亚型。在实验模型中证实了I组受体拮抗剂(mGluR1和mGluR5)以及II组受体激动剂(mGluR2和mGluR3)和III组受体激动剂(mGluR4、mGluR6、mGluR7和mGluR8)的抗惊厥作用。临床前数据还远未完成,但明确的抗惊厥作用和无严重副作用支持进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Metabotropic glutamate receptors as a possible target of antiepileptic therapy].

Antagonists of glutamate ionotropic receptors exhibit marked anticonvulsant action but also serious side effects, therefore attention is shifted to drugs influencing metabotropic glutamate receptors. These receptors are classified into three groups (I-III) and eight subtypes. Anticonvulsant action in experimental models was demonstrated for antagonists of group I receptors (mGluR1 and mGluR5) as well as for agonists of groups II (mGluR2 and mGluR3) and III (mGluR4, mGluR6, mGluR7 and mGluR8). Preclinical data are far from being complete but clear anticonvulsant action and absence of serious side effects speak in favor of further research.

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