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[精神药物作用下大鼠大脑皮质离体神经末梢中H3-γ-氨基丁酸的释放]

[Liberation of H3-GABA from isolated nerve endings of the cerebral cortex of rats under the effect of psychotropic drugs].

作者信息

Maĭsov N I, Tolmacheva N S, Raevskiĭ K S

出版信息

Farmakol Toksikol. 1976 Sep-Oct;39(5):517-20.

PMID:1028577
Abstract

The influence of a number of neuroleptics and antidepressants on the release of 3H-GABA from the synaptosomas of the cerebral cortex in rats was studied. Chlorpromazine, phthorphenazine, trifluperidol, imipramine, phthoracizine caused an intensified liberation of 3H-GABA from the synaptosomas. In this phenothiazine neuroleptics proved more active than did trifluperidol and antidepressants. New neuroleptics--azabuperon and carbidine and also diphenylhydantoin tended to restrict the liberation of the mediator from synaptosomas. The tranquilizer diazepam, gamma-oxybutyric acid and carbamazepine failed to have any significnat effect on this process. The described effects of thepsychotropic substances are due, apparently, to their direct influence on the synaptomal membrane.

摘要

研究了多种神经阻滞剂和抗抑郁药对大鼠大脑皮质突触体中3H-γ-氨基丁酸(3H-GABA)释放的影响。氯丙嗪、酞哌嗪、三氟哌多、丙咪嗪、酞嗪嗪可使突触体中3H-GABA的释放增强。在这方面,吩噻嗪类神经阻滞剂比三氟哌多和抗抑郁药更具活性。新型神经阻滞剂——氮杂丁苯酮和卡比啶以及苯妥英倾向于限制介质从突触体中的释放。镇静剂地西泮、γ-羟基丁酸和卡马西平对这一过程没有任何显著影响。这些精神药物所描述的作用显然是由于它们对突触体膜的直接影响。

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