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腹内侧下丘脑在介导抗焦虑药物在不同焦虑模型中的抗厌恶作用方面的神经化学特征。

Neurochemical characteristics of the ventromedial hypothalamus in mediating the antiaversive effects of anxiolytics in different models of anxiety.

作者信息

Talalaenko A N, Pankrat'ev D V, Goncharenko N V

机构信息

Department of Pharmacology and Clinical Pharmacology, M. Gor'kii Medical University, 16 Il'ich Prospekt, 83003 Donetsk, Ukraine.

出版信息

Neurosci Behav Physiol. 2003 Mar;33(3):255-61. doi: 10.1023/a:1022151331354.

Abstract

In experiments on rats using an "illuminated area" avoidance test and a "threatening situation" avoidance test, preliminary i.p. administration and subsequent microinjection into the ventromedial hypothalamus of various combinations of monoamines, transmitter amino acids, and their agonists and antagonists demonstrated differences in the functional importance of the neurochemical profile of this limbic formation in mediating anxiety states of different origins. The neurochemical analysis with local intrahypothalamic administration of anxiosedative and anxioselective substances showed that the antiaversive actions of Campirone are obtained only in conditions in which the dominant motivation is fear, while chlordiazepoxide, Phenibut, and Indoter are also active in anxiety induced by negatively stressful zoosocial influences; these actions are mediated respectively by serotoninergic and GABAergic types of synaptic switching in the ventromedial hypothalamus.

摘要

在大鼠实验中,采用“光照区域”回避试验和“威胁情境”回避试验,通过腹腔内预先给药,随后向腹内侧下丘脑微量注射单胺、递质氨基酸及其激动剂和拮抗剂的各种组合,结果表明,该边缘结构的神经化学特征在介导不同来源焦虑状态时,其功能重要性存在差异。通过下丘脑局部给药抗焦虑和抗焦虑选择性物质进行神经化学分析表明,只有在主导动机为恐惧的条件下,才能获得坎皮隆的抗厌恶作用,而氯氮卓、苯乙哌啶酮和因多替在负面应激性社会环境影响诱发的焦虑中也有活性;这些作用分别由腹内侧下丘脑的5-羟色胺能和γ-氨基丁酸能突触转换介导。

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