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育亨宾会损害正常受试者的P50听觉感觉门控。

Yohimbine impairs P50 auditory sensory gating in normal subjects.

作者信息

Adler L E, Hoffer L, Nagamoto H T, Waldo M C, Kisley M A, Giffith J M

机构信息

University of Colorado Health Sciences Center Department of Psychiatry, Denver 80262.

出版信息

Neuropsychopharmacology. 1994 Jul;10(4):249-57. doi: 10.1038/npp.1994.28.

Abstract

The evoked response to repeated auditory stimuli generally decreases in amplitude, a phenomenon that demonstrates the activity of sensory gating mechanisms in the central nervous system (CNS). Gating of the P50 wave of the auditory evoked response shows such behavior in normals, but not in schizophrenic or manic subjects. In mania, diminished gating of the auditory evoked response is correlated with elevated levels of noradrenergic metabolites. In animals, yohimbine, a presynaptic alpha-2 antagonist, increases noradrenergic neuronal transmission in the CNS and diminished gating of the auditory evoked response. The aim of this experiment was to test whether yohimbine causes diminished auditory sensory gating in normal human controls. Seven normal subjects with normal P50 auditory gating were treated either with 0.4 mg/kg of oral yohimbine on one day or placebo on a different day. Each subject acted as his own control. Yohimbine, but not placebo, caused a significant but transient decrease in P50 auditory gating in these subjects. Thus, increasing CNS noradrenergic neuronal transmission in normal controls can cause a transient impairment in auditory sensory gating.

摘要

对重复听觉刺激的诱发反应,其振幅通常会降低,这一现象表明中枢神经系统(CNS)中存在感觉门控机制的活动。听觉诱发反应中P50波的门控在正常人中呈现出这样的行为,但在精神分裂症患者或躁狂症患者中则不然。在躁狂症中,听觉诱发反应的门控减弱与去甲肾上腺素能代谢产物水平升高相关。在动物实验中,育亨宾,一种突触前α-2拮抗剂,会增加中枢神经系统中去甲肾上腺素能神经元的传递,并减弱听觉诱发反应的门控。本实验的目的是测试育亨宾是否会导致正常人类对照组的听觉感觉门控减弱。七名P50听觉门控正常的正常受试者,在某一天接受0.4mg/kg的口服育亨宾治疗,在另一天接受安慰剂治疗。每个受试者都作为自己的对照。育亨宾而非安慰剂,导致这些受试者的P50听觉门控出现显著但短暂的降低。因此,在正常对照组中增加中枢神经系统去甲肾上腺素能神经元的传递,可导致听觉感觉门控出现短暂损害。

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