Two weeks of pretreatment with escitalopram facilitates extinction learning in healthy individuals
Abstract
OBJECTIVE: We aimed to examine whether pretreatment with escitalopram would be associated with reduced fear acquisition and enhanced extinction learning in a fear conditioning paradigm, compared with placebo. METHODS: Healthy volunteers were randomized in double-blind fashion, to 14 days of escitalopram 10 mg/day (n = 18) or placebo (n = 20) prior to a classical fear conditioning paradigm. RESULTS: Although escitalopram was associated with a smaller skin conductance (SC) orienting response during habituation, no medication effects on fear acquisition were found. Escitalopram was associated with faster extinction of SC responses, compared with placebo, as revealed by a significant drug × conditioned stimulus × trial interaction for early extinction (F(3, 30) = 3.26, p = 0.035) and late extinction (F(3, 30) = 3.27, p = 0.035) trials. After adjustment for age, orienting response, and acquisition, results from linear contrast remained significant for early extinction (F(1, 29) = 5.43, p = 0.027). CONCLUSIONS: Escitalopram administered for 14 days prior to a fear conditioning paradigm did not influence acquisition of a conditioned fear response but did facilitate extinction learning. Impairments in extinction learning have been identified as a key component of posttraumatic stress disorder; our preliminary findings suggest that additional experimental and clinical studies assessing the efficacy of selective serotonin reuptake inhibitors for posttraumatic stress disorder prevention are warranted.
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There is some evidence from skin conductance-based investigations suggesting a facilitatory role of antidepressants in fear extinction learning.
“Although the use of antidepressants has not been widely studied in extinction of fear-potentiated startle studies, there is some evidence from skin conductance-based investigations suggesting a facilitatory role of these drugs in fear extinction learning (82).”
From Conditioned fear associated phenotypes as robust, translational indices of trauma-, stressor-, and anxiety-related behaviors (2014) · cites this paper as [82]
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References 45 · Cited by 42
- Authors
- Bui, E., Orr, S. P., Jacoby, R. J., Keshaviah, A., LeBlanc, N. J., Milad, M. R., Pollack, M. H., & Simon, N. M.
- Affiliations
- Center for Anxiety and Traumatic Stress Disorders Massachusetts General Hospital Boston Massachusetts USA
- Harvard University (US)
- Massachusetts General Hospital (US)
- Rush University Medical Center (US)
- ORCID
- Venue
- Human Psychopharmacology Clinical and Experimental
- Publisher
- Wiley
- Published
- 2013-06-15
- Volume
- 28
- Issue
- 5
- Pages
- 447-456
- ISSN
- 0885-6222 (ISSN-L)
- 1099-1077
- OpenAlex
- W2132706865
- Cited by
- 42
- References
- 45
- Citations by year
- 2025: 2 · 2024: 1 · 2023: 6 · 2022: 2 · 2021: 6 · 2020: 1 · 2019: 4 · 2018: 1 · 2017: 3 · 2016: 4 · 2015: 4 · 2014: 6 · 2013: 2
- FWCI
- 2.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Human Psychopharmacology Clinical and Experimental (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Centre Hospitalier Universitaire de Toulouse
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- escitalopram, extinction learning, fear conditioning, fear acquisition, selective serotonin reuptake inhibitors, skin conductance, orienting response, post-traumatic stress disorder, healthy volunteers
- MeSH terms
- Adult, Conditioning, Psychological, Double-Blind Method, Extinction, Psychological, Fear, Female, Humans, Learning, Male, Middle Aged, Citalopram, Selective Serotonin Reuptake Inhibitors, Young Adult
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