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同型半胱氨酸:立体异构体对小鼠的惊厥作用。

Homocysteic acid: convulsant action of stereoisomers in mice.

作者信息

Turski W A

机构信息

Department of Pharmacology, Medical School, Lublin, Poland.

出版信息

Brain Res. 1989 Feb 13;479(2):371-3. doi: 10.1016/0006-8993(89)91643-0.

Abstract

An effect of excitatory amino acid antagonists, 2-amino-7-phosphonoheptanoate (AP7), a selective N-methyl-D-aspartate (NMDA) antagonist, and gamma-D-glutamylaminomethylsulphonate (gamma-D-GAMS), a preferential kainate/quisqualate antagonist, on convulsions induced by intracerebroventricular administration of stereoisomers of homocysteic acid (HCA) was tested in mice. AP7, 0.025 mumol, blocked myoclonic seizures induced by L-HCA and D,L-HCA, and had no anticonvulsant action against D-HCA, gamma-D-GAMS, 0.5 mumol, was preferentially active against myoclonic seizures induced by D-HCA, had moderate anticonvulsant action against D,L-HCA, and no effect against seizures induced by L-HCA. These results indicate that activation of NMDA receptors contributes substantially to the convulsant action of L-HCA, while the convulsant action of D-HCA may be mediated mainly by non-NMDA related mechanisms.

摘要

在小鼠中测试了兴奋性氨基酸拮抗剂2-氨基-7-磷酸庚酸(AP7,一种选择性N-甲基-D-天冬氨酸(NMDA)拮抗剂)和γ-D-谷氨酰胺甲基磺酸盐(γ-D-GAMS,一种优先的海人藻酸/quisqualate拮抗剂)对脑室内注射高半胱氨酸(HCA)立体异构体诱导的惊厥的影响。0.025微摩尔的AP7可阻断由L-HCA和D,L-HCA诱导的肌阵挛性癫痫发作,而对D-HCA没有抗惊厥作用;0.5微摩尔的γ-D-GAMS对由D-HCA诱导的肌阵挛性癫痫发作具有优先活性,对D,L-HCA具有中等抗惊厥作用,而对由L-HCA诱导的癫痫发作没有影响。这些结果表明,NMDA受体的激活在很大程度上促成了L-HCA的惊厥作用,而D-HCA的惊厥作用可能主要由非NMDA相关机制介导。

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