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育亨宾可促进患有创伤后应激障碍的退伍军人的听觉惊吓反应。

Yohimbine facilitated acoustic startle in combat veterans with post-traumatic stress disorder.

作者信息

Morgan C A, Grillon C, Southwick S M, Nagy L M, Davis M, Krystal J H, Charney D S

机构信息

National Center for Post-Traumatic Stress Disorder, West Haven VA Medical Center, CT 06516, USA.

出版信息

Psychopharmacology (Berl). 1995 Feb;117(4):466-71. doi: 10.1007/BF02246220.

DOI:10.1007/BF02246220
PMID:7604149
Abstract

Preclinical and clinical studies have suggested that the acoustic startle reflex (ASR) is a useful model to investigate the neurochemical basis of anxiety and fear states. This work has revealed that the anxiogenic alpha-2 receptor antagonist, yohimbine, increases the amplitude of the ASR in laboratory animals and in healthy human controls. Because of the growing body of data that support the hypothesis that severe stress results in substantial alterations in noradrenergic neuronal reactivity, the present investigation evaluated the effects of yohimbine on the ASR of 18 patients with PTSD and 11 healthy combat controls. Subjects received IV yohimbine (0.4 mg/kg) or saline placebo on 2 separate days in a randomized double blind placebo control design. A trial of two tone frequencies with varied intensity (90, 96, 102, 108, 114 dB) white noise and instantaneous rise time, was delivered binaurally through headphones. Tones were delivered every 25-60 s, for a 40-ms duration. Startle testing was performed 80 min post-infusion and lasted 15-20 min. Yohimbine significantly increased the amplitude, magnitude and probability of the ASR in combat veterans with PTSD, but did not do so in combat controls. Overall startle was significantly larger in the PTSD subjects; however, this did not account for the differential effect of yohimbine, since yohimbine had no significant effect in the control group. This study demonstrates an excitatory effect of yohimbine on the amplitude, magnitude and probability of the ASR in PTSD patients that is not seen in combat controls.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

临床前和临床研究表明,听觉惊吓反射(ASR)是一种用于研究焦虑和恐惧状态神经化学基础的有用模型。这项工作揭示,致焦虑的α-2受体拮抗剂育亨宾可增加实验动物和健康人类对照中ASR的幅度。由于越来越多的数据支持严重应激会导致去甲肾上腺素能神经元反应性发生实质性改变这一假设,本研究评估了育亨宾对18名创伤后应激障碍(PTSD)患者和11名健康参战对照者ASR的影响。在随机双盲安慰剂对照设计中,受试者在2个不同日期接受静脉注射育亨宾(0.4mg/kg)或生理盐水安慰剂。通过耳机双耳给予两种不同强度(90、96、102、108、114dB)白噪声且上升时间瞬间变化的音调频率试验。音调每25 - 60秒发出一次,持续40毫秒。在输注后80分钟进行惊吓测试,持续15 - 20分钟。育亨宾显著增加了患有PTSD的参战退伍军人ASR的幅度、大小和概率,但在参战对照者中未出现这种情况。PTSD受试者的总体惊吓反应明显更大;然而,这并不能解释育亨宾的差异效应,因为育亨宾在对照组中没有显著影响。这项研究表明,育亨宾对PTSD患者ASR的幅度、大小和概率具有兴奋作用,而在参战对照者中未观察到这种作用。(摘要截选至250字)

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