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箭毒化猫外侧膝状体中的药物与PGO波。V. 其他化合物。中枢神经递质对PGO波活动作用的概述。

Drugs and PGO waves in the lateral geniculate body of the curarized cat. V. Miscellaneous compounds. Synopsis of the role of central neurotransmitters on PGO wave activity.

作者信息

Ruch-Monachon M A, Jalfre M, Haefely W

出版信息

Arch Int Pharmacodyn Ther. 1976 Feb;219(2):326-46.

PMID:5977
Abstract

In the last part of this series we have studied the effects of various drugs on ponto-geniculo-occipital (PGO) waves induced by the benzoquinolizine derivative, Ro 4-1284 (PGO(1284)), and by the inhibitor of trypotophan hydroxylase, p-chlorophenylalanine (PGO(PCPA)), and continuously recorder and counted in the lateral geniculate bodies (LGB) of unanaesthetized and immobilizedcats. The major aim of this study was to test the specificity of drug-induced alterations of the PGO wave activity suggested by the previous investigations. Hypnotics-sedatives of different classes had no significant effects in doses that did not markedly alter the electrical background activity in the LGB. A notable exception was gamma-hydroxybutyric acid which increased the density of PGO(1284) and PGO(PCPA). A number of neuroleptics were found inactive; sulpiride surprisingly decreased the density of PGO(1284). Bulbocapnine had a similar effect. Convulsants in subconvulsive doses did not uniformly affect PGO waves; while pentetrazole had no consistent effect, strychnine decreased and picrotoxin increased the density of PGO(1284). High doses of morphine, methadone and meperidine decreased the PGO(1284). Ethanol was inactive even in high doses. Caffeine and mefexamide reduced the density of PGO(1284). Mepiprazol was the most potent depressant of PGO(1284, probably by inhibiting the uptake of 5-HT. Mescaline was a weak depressor of PGO(1284). p-Chloromethamphetamine induced PGO waves in untreated cats less consitently than did PCPA. Amantadine reduced the amplitude of PGO waves due to a central antinicotinic action. The results of this study and of the whole series suggested a tentative scheme of the generation and modulation of PGO waves, in which the hypothetical roles and sites of action of four central neurotransmitters are included.

摘要

在本系列研究的最后一部分,我们研究了各种药物对由苯并喹嗪衍生物Ro 4-1284(PGO(1284))和色氨酸羟化酶抑制剂对氯苯丙氨酸(PGO(PCPA))诱导的脑桥-膝状体-枕叶(PGO)波的影响,并在未麻醉和固定的猫的外侧膝状体(LGB)中进行连续记录和计数。本研究的主要目的是检验先前研究所提示的药物诱导的PGO波活动改变的特异性。不同类别的催眠镇静剂在未明显改变LGB电背景活动的剂量下无显著影响。一个显著的例外是γ-羟基丁酸,它增加了PGO(1284)和PGO(PCPA)的密度。发现多种抗精神病药物无活性;舒必利出人意料地降低了PGO(1284)的密度。荷包牡丹碱有类似作用。亚惊厥剂量的惊厥剂对PGO波的影响并不一致;戊四氮没有一致的作用,士的宁降低而印防己毒素增加了PGO(1284)的密度。高剂量的吗啡、美沙酮和哌替啶降低了PGO(1284)。乙醇即使高剂量也无活性。咖啡因和甲非酰胺降低了PGO(1284)的密度。美吡拉佐是PGO(1284)最有效的抑制剂,可能是通过抑制5-羟色胺的摄取。三甲氧苯乙胺是PGO(1284)的弱抑制剂。对氯甲基苯丙胺在未处理的猫中诱导PGO波的一致性不如对氯苯丙氨酸。金刚烷胺由于中枢抗烟碱作用降低了PGO波的振幅。本研究及整个系列的结果提示了一个PGO波产生和调节的初步方案,其中包括四种中枢神经递质的假定作用和作用位点。

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