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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...

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Autores principales: Lippold, Julia V., Ettinger, Ulrich, Hurlemann, René, Corr, Philip J., Reuter, Martin, Perkins, Adam M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303801/
https://www.ncbi.nlm.nih.gov/pubmed/32596627
http://dx.doi.org/10.1017/pen.2020.1
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author Lippold, Julia V.
Ettinger, Ulrich
Hurlemann, René
Corr, Philip J.
Reuter, Martin
Perkins, Adam M.
author_facet Lippold, Julia V.
Ettinger, Ulrich
Hurlemann, René
Corr, Philip J.
Reuter, Martin
Perkins, Adam M.
author_sort Lippold, Julia V.
collection PubMed
description 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(mean) 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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spelling pubmed-73038012020-06-26 Differentiating anxiety from fear: an experimental–pharmacological approach Lippold, Julia V. Ettinger, Ulrich Hurlemann, René Corr, Philip J. Reuter, Martin Perkins, Adam M. Personal Neurosci Empirical Paper 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(mean) 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. Cambridge University Press 2020-06-17 /pmc/articles/PMC7303801/ /pubmed/32596627 http://dx.doi.org/10.1017/pen.2020.1 Text en © The Author(s) 2020 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Empirical Paper
Lippold, Julia V.
Ettinger, Ulrich
Hurlemann, René
Corr, Philip J.
Reuter, Martin
Perkins, Adam M.
Differentiating anxiety from fear: an experimental–pharmacological approach
title Differentiating anxiety from fear: an experimental–pharmacological approach
title_full Differentiating anxiety from fear: an experimental–pharmacological approach
title_fullStr Differentiating anxiety from fear: an experimental–pharmacological approach
title_full_unstemmed Differentiating anxiety from fear: an experimental–pharmacological approach
title_short Differentiating anxiety from fear: an experimental–pharmacological approach
title_sort differentiating anxiety from fear: an experimental–pharmacological approach
topic Empirical Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303801/
https://www.ncbi.nlm.nih.gov/pubmed/32596627
http://dx.doi.org/10.1017/pen.2020.1
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