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顺式-2,3-哌啶二羧酸对兴奋性氨基酸诱导的脊髓神经元兴奋及突触兴奋的拮抗作用。

Antagonism of excitatory amino acid-induced and synaptic excitation of spinal neurones by cis-2,3-piperidine dicarboxylate.

作者信息

Davies J, Evans R H, Francis A A, Jones A W, Watkins J C

出版信息

J Neurochem. 1981 Mar;36(3):1305-7. doi: 10.1111/j.1471-4159.1981.tb01736.x.

Abstract

In tests on neurones in the cat spinal cord in vivo, and frog and immature rat spinal cord in vitro, cis-2,3-piperidine dicarboxylate (cis-2,3-PDA) produced the following effects: (1) selective antagonism of amino acid-induced responses, compared with responses to other putative transmitters; (2) effective antagonism of kainate and quisqualate-induced responses in addition to responses induced by N-methyl-D-aspartate (NMDA) and other excitatory amino acids; (3) partial NMDA-like agonist action; (4) antagonism of dorsal root-evoked excitation of Renshaw cells; (5) potentiation of acetylcholine- and ventral root-evoked excitation of Renshaw cells. This unique spectrum of action may be useful for transmitter receptor characterization in the vertebrate central nervous system.

摘要

在对猫脊髓运动神经元进行的体内试验以及对青蛙和未成熟大鼠脊髓进行的体外试验中,顺式-2,3-哌啶二羧酸(cis-2,3-PDA)产生了以下效应:(1)与对其他假定递质的反应相比,对氨基酸诱导的反应具有选择性拮抗作用;(2)除了对N-甲基-D-天冬氨酸(NMDA)和其他兴奋性氨基酸诱导的反应外,对海人藻酸和quisqualate诱导的反应也具有有效拮抗作用;(3)部分类似NMDA的激动剂作用;(4)拮抗背根诱发的闰绍细胞兴奋;(5)增强乙酰胆碱和腹根诱发的闰绍细胞兴奋。这种独特的作用谱可能有助于脊椎动物中枢神经系统中递质受体的特性鉴定。

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