区分焦虑与恐惧:一种实验药理学方法。

Q3 Medicine
Personality Neuroscience Pub Date : 2020-06-17 eCollection Date: 2020-01-01 DOI:10.1017/pen.2020.1
Julia V Lippold, Ulrich Ettinger, René Hurlemann, Philip J Corr, Martin Reuter, Adam M Perkins
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引用次数: 7

摘要

格雷的人格理论假设恐惧和焦虑是截然不同的情绪系统,只有后者对抗焦虑药物敏感。他的工作主要基于动物研究,证实他的理论的转化研究很少。先前的人类研究表明,苯二氮卓类药物劳拉西泮对这两个系统的影响取决于剂量(1和2毫克)和消极情绪的个性差异。本研究旨在重复这些发现,并通过引入较低剂量的0.5 mg劳拉西泮来测试药物阈值效应。50名健康成人(23名男性,平均22.40岁,SD±3.68)参与了分离风险评估强度(RAI,反映焦虑)和逃跑强度(FI,反映恐惧)的实验威胁-回避范式,并完成了两份评估负面情绪方面的自我报告问卷(Spielberger状态-特质焦虑量表和恐惧量表)。在受试者内随机安慰剂对照设计中,每天应用0.5和1mg劳拉西泮。为了控制镇静药物的作用,用眼动追踪法测定了跳跃性峰值速度。结果显示劳拉西泮对RAI有预期的特异性抗焦虑作用,但仅在0.5 mg的情况下有效。劳拉西泮对FI没有影响,先前关于劳拉西泮与自我报告的消极情绪相互作用的发现无法得到证实。总的来说,本研究表明,在使用转化行为任务时,在没有药物效应的情况下,剂量≤1mg的劳拉西泮具有抗焦虑作用。然而,人格对防御行为的调节作用需要在未来的研究中得到澄清。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Differentiating anxiety from fear: an experimental-pharmacological approach.

Differentiating anxiety from fear: an experimental-pharmacological approach.

Differentiating anxiety from fear: an experimental-pharmacological approach.

Differentiating anxiety from fear: an experimental-pharmacological approach.

Gray's theory of personality postulates that fear and anxiety are distinct emotional systems with only the latter being sensitive to anxiolytic drugs. His work was mainly based on animal research, and translational studies validating his theory are scarce. Previous work in humans showed an influence of the benzodiazepine lorazepam on both systems, however, dependent on dosage (1 and 2 mg) and personality differences in negative emotionality. The present study aims to replicate these findings, and in addition tests the drug threshold effect by introducing a lower dosage of 0.5 mg lorazepam. Fifty healthy adults (23 males, agemean 22.40, SD ± 3.68) participated in an experimental threat-avoidance paradigm designed to dissociate risk assessment intensity (RAI, reflecting anxiety) and flight intensity (FI, reflecting fear) and completed two self-report questionnaires assessing facets of negative emotionality (Spielberger State Trait Anxiety Inventory and Fear Survey Schedule). In a randomized placebo-controlled within-subjects design, 0.5 and 1 mg of lorazepam were applied per os. Saccadic peak velocity was assessed by means of eye-tracking in order to control for sedating drug effects. Results showed the expected and specific anxiolytic effect of lorazepam on RAI, however, only in the 0.5 mg condition. FI was not influenced by lorazepam, and previous findings of interaction effects of lorazepam with self-reported negative emotionality could not be corroborated. Overall, this study demonstrates anxiolytic effects of lorazepam in dosages ≤1 mg in the absence of a drug effect on fear using a translational behavioural task. However, a putative moderating role of personality on defensive behaviour has to be clarified in future research.

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来源期刊
Personality Neuroscience
Personality Neuroscience Medicine-Neurology (clinical)
CiteScore
2.90
自引率
0.00%
发文量
4
审稿时长
6 weeks
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