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Differentiating anxiety from fear: an experimental–pharmacological approach

机译:将焦虑与恐惧区分开来:实验-药理学方法

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摘要

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, age 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 ( and ). 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.
机译:格雷的人格理论假设,恐惧和焦虑是不同的情绪系统,只有后者对抗焦虑药敏感。他的工作主要是基于动物研究,而验证他的理论的转化研究却很少。先前在人体中的研究表明,苯二氮卓类劳拉西m对两种系统都有影响,但是,这取决于剂量(1和2 mg)以及负面情绪的人格差异。本研究旨在复制这些发现,并通过引入较低剂量的0.5 mg劳拉西m来测试药物阈值作用。五十名健康的成年人(23名男性,22.40岁,SD±3.68)参加了实验避免威胁范式,旨在分离风险评估强度(RAI,反映焦虑)和飞行强度(FI,反映恐惧),并完成了两份自我报告调查表评估负面情绪的各个方面(和)。在随机安慰剂对照的受试者内部设计中,每剂口服0.5和1 mg劳拉西m。为了控制镇静药物作用,通过眼动追踪评估了排骨峰值速度。结果显示劳拉西m对RAI具有预期和特异性的抗焦虑作用,但是仅在0.5 mg条件下有效。 FI不受劳拉西m的影响,以前证实劳拉西m与自我报告的负性情绪有交互作用的结果不能得到证实。总的来说,这项研究表明,劳拉西m在≤1 mg剂量下的抗焦虑作用不存在使用平移行为任务对恐惧的药物作用。然而,在未来的研究中必须阐明人格对防御行为的调节作用。

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