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[腹侧苍白球在不同焦虑模型中实现抗焦虑药抗厌恶作用的神经化学特征]

[Neurochemical features of the ventral pallidum in realization of the antiaversive effects of anxiolytics in different models of anxiety].

作者信息

Talalaenko A N, Pankrat'ev D V, Bulgakova N P

出版信息

Eksp Klin Farmakol. 2006 Jan-Feb;69(1):6-11.

Abstract

Preliminary intraperitoneal injections of some combinations of adreno- and dopaminomimetics, monoamines, and mediator amino acids (as well as of their agonists and antagonists) followed by microinjections of the same combinations into the ventral pallidum reveal differences in the functional significance of the neurochemical profile of this paleostriatum formation in realization of the anxiety states of different genesis, as manifested in the "illuminated site avoidance" and the "threatening situation" tests in rats. The pharmacological analysis based on the local injection of anxiosedative and anxioselective agents into the ventral paleostriatum showed that the antiaversive action of campirone is revealed under the conditions of dominating fear motivation, while that analogous action of chlordiazepoxide, phenibut and indoter is revealed under negative stressful zoosocial impacts and is realized by serotonin- and GABA-ergic (rather than by cathecholamine- and glutaminergic) aversive systems of the ventral pallidum.

摘要

预先腹腔注射某些肾上腺素能和多巴胺能模拟物、单胺以及介质氨基酸的组合(以及它们的激动剂和拮抗剂),随后向腹侧苍白球微量注射相同组合,结果显示,在大鼠的“光照位点回避”和“威胁情境”测试中,这种古纹状体结构的神经化学特征在不同起源的焦虑状态实现过程中的功能意义存在差异。基于向腹侧苍白球局部注射抗焦虑和抗焦虑选择性药物的药理学分析表明,在恐惧动机占主导的情况下,坎皮隆表现出抗厌恶作用,而氯氮卓、苯乙胺和吲哚的类似作用则在负面应激性社会环境影响下表现出来,并通过腹侧苍白球的5-羟色胺能和γ-氨基丁酸能(而非儿茶酚胺能和谷氨酰胺能)厌恶系统实现。

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