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皮层应用N-甲基-D-天冬氨酸拮抗剂的抗惊厥作用中无副作用。

Absence of side-effects in the anticonvulsant action of cortically applied antagonists of N-methyl-D-aspartate.

作者信息

Frenk H, Liban A, Urca G, Teichberg V I

出版信息

Brain Res. 1986 May 14;373(1-2):222-6. doi: 10.1016/0006-8993(86)90334-3.

Abstract

Three compounds reportedly blocking the N-methyl-D-aspartate (NMDA) receptor, namely 2-amino-5-phosphonovalerate, gamma-D-glutamylglycine and 3-hydroxy-2-quinoxalinecarboxylic acid, were injected subdurally onto the cortex of freely moving rats. All 3 compounds effectively suppressed behavioral and electrographic seizure activity induced by strychnine, morphine and picrotoxin that were administered via the same route. The cortical application of the NMDA-receptor antagonists did not induce behavioral or electrographic changes, and behavioral side-effects commonly observed following intracerebroventricular administration of these compounds were absent. The anatomical separation of anticonvulsant action and side-effects induced by these compounds suggests that this class of compounds may eventually be useful as antiepileptic drugs.

摘要

据报道,三种可阻断N-甲基-D-天冬氨酸(NMDA)受体的化合物,即2-氨基-5-磷酸戊酸、γ-D-谷氨酰甘氨酸和3-羟基-2-喹喔啉羧酸,被硬膜下注射到自由活动大鼠的大脑皮层。所有这三种化合物均有效抑制了通过相同途径给药的士的宁、吗啡和印防己毒素所诱导的行为和脑电图癫痫活动。NMDA受体拮抗剂的皮层应用未诱发行为或脑电图变化,且不存在这些化合物脑室内给药后常见的行为副作用。这些化合物所诱导的抗惊厥作用和副作用在解剖学上的分离表明,这类化合物最终可能可用作抗癫痫药物。

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