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环状二羧酸对大鼠皮层神经元自发活动和氨基酸诱发活动的影响。

The effects of cyclic dicarboxylic acids on spontaneous and amino acid-evoked activity of rat cortical neurones.

作者信息

Birley S, Collins J F, Perkins M N, Stone T W

出版信息

Br J Pharmacol. 1982 Sep;77(1):7-12. doi: 10.1111/j.1476-5381.1982.tb09262.x.

Abstract

1 A series of cyclic dicarboxylic acids were applied by microiontophoresis to neurones in the cerebral cortex of rats anaesthetized with urethane. The object was to examine effects on spontaneous firing rates and any ability to antagonize responses to excitatory amino acids. 2 At relatively low ejecting currents (10-25 nA) cis-2,3-piperidine dicarboxylic acid (cis-2,3-PDA) had no effect on spontaneous firing but selectively antagonized the excitation evoked by n-methyl-D-aspartate (NMDA) without affecting responses to quisqualaife or kainate. At higher ejecting currents (60-100 nA) responses to all three agonists were reduced. 3 Other cis-piperidine dicarboxylic acids and piperazine-2,3-dicarboxylic acid had only weak and variable effects on cell firing and responses to NMDA, quisqualate, kainate, glutamate and aspartate. 4 2, 3-Pyridine dicarboxylic acid (quinolinic acid) produced excitation of all cortical neurones tested. 5 2-Amino-5-phosphono-valeric acid, an NMDA antagonist, reduced responses to quinolinate, implying that this compound can act at NMDA receptors. 6 It is suggested that quinolinic acid may be of physiological interest as a potential endogenous excitant in the nervous system and that cis-2,3-PDA and its N-methyl derivative may be of use in studies of receptor pharmacology and the identification of synaptic transmitters.

摘要
  1. 采用微量离子电泳法将一系列环状二羧酸施加于用氨基甲酸乙酯麻醉的大鼠大脑皮质神经元上。目的是研究其对自发放电率的影响以及拮抗兴奋性氨基酸反应的能力。2. 在相对较低的喷射电流(10 - 25纳安)下,顺式 - 2,3 - 哌啶二羧酸(cis - 2,3 - PDA)对自发放电无影响,但能选择性拮抗由N - 甲基 - D - 天冬氨酸(NMDA)诱发的兴奋,而不影响对喹啉酸或 kainate的反应。在较高的喷射电流(60 - 100纳安)下,对所有三种激动剂的反应均降低。3. 其他顺式哌啶二羧酸和哌嗪 - 2,3 - 二羧酸对细胞放电以及对NMDA、喹啉酸、kainate、谷氨酸和天冬氨酸的反应只有微弱且多变的影响。4. 2,3 - 吡啶二羧酸(喹啉酸)使所有测试的皮质神经元兴奋。5. NMDA拮抗剂2 - 氨基 - 5 - 磷酸戊酸降低了对喹啉酸盐的反应,这表明该化合物可作用于NMDA受体。6. 有人提出,喹啉酸作为神经系统中潜在的内源性兴奋物可能具有生理意义,而顺式 - 2,3 - PDA及其N - 甲基衍生物可能在受体药理学研究和突触递质鉴定中有用。

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