毒蕈碱受体对惊厥药3-巯基丙酸的区域依赖性中枢神经系统膜反应。

P G Schneider, G Rodríguez de Lores Arnaiz
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引用次数: 3

摘要

已有研究表明,以150 mg/kg剂量给药惊厥药3-巯基丙酸可增强毒蕈碱拮抗剂[3H]喹啉苄酯([3H]QNB)与某些大鼠中枢神经系统膜的结合亲和力,而不影响位点数。本研究采用100 mg/kg剂量,并测试了[3H]QNB与癫痫发作前、癫痫发作和癫痫发作后死亡大鼠的小脑、海马和纹状体膜的结合。在小脑中,在癫痫发作前、发作和发作后阶段,结合分别增加24%、65%和19%;在海马中,癫痫发作前和发作后的数值分别高出12%和20%,但与对照组没有差异;纹状体在发作和发作后分别增加了10%和18%,而在发作前没有变化。亚惊厥剂量(20mg /kg)和体外药物添加对结合均无影响。结果表明对惊厥的不同反应,小脑和海马的可逆变化,纹状体的延迟反应,支持区域依赖神经元可塑性的概念。
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Area-dependent CNS membrane response of muscarinic receptor to convulsant 3-mercaptopropionic acid.

It has already been shown that the administration of convulsant 3-mercaptopropionic acid at 150 mg/kg enhances binding affinity of muscarinic antagonist [3H]quinuclidinyl benzilate ([3H]QNB) to certain rat CNS membranes without affecting site number. Herein we employed a 100 mg/kg dose and tested [3H]QNB binding to cerebellar, hippocampal, and striatal membranes obtained from rats killed at preseizure, seizure, and postseizure stages. In cerebellum, binding increased 24, 65, and 19% a1 preseizure, seizure, and postseizure stages, respectively; in hippocampus, values were 12 and 20% higher at pre- and seizure stages, but failed to differ from controls at postseizure; in striatum, increases of 10 and 18% were recorded at seizure and postseizure, with no changes at preseizure. Neither a subconvulsant dose (20 mg/kg) nor in vitro drug addition had any effect on binding. Results indicate a differential response to the convulsant, with reversible changes in cerebellum and hippocampus, and a delayed response in striatum, supporting the concept of area-dependent neuronal plasticity.

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