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Anti-Intrusion Effect of Lorazepam: An Experimental Study
OBJECTIVE: Easy triggering of trauma-related episodic memory fragments caused by perceptual cues is tied to strong perceptual priming in the implicit memory system. And among benzodiazepines, only lorazepam has been consistently reported to have an atypical suppression effect on perceptual priming p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neuropsychiatric Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843020/ https://www.ncbi.nlm.nih.gov/pubmed/24302951 http://dx.doi.org/10.4306/pi.2013.10.3.273 |
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author | Lee, Hong-Seock Lee, Heung-Pyo Lee, Sang-Kyu Kim, Yong-Ku Choi, Yun-Kyeung |
author_facet | Lee, Hong-Seock Lee, Heung-Pyo Lee, Sang-Kyu Kim, Yong-Ku Choi, Yun-Kyeung |
author_sort | Lee, Hong-Seock |
collection | PubMed |
description | OBJECTIVE: Easy triggering of trauma-related episodic memory fragments caused by perceptual cues is tied to strong perceptual priming in the implicit memory system. And among benzodiazepines, only lorazepam has been consistently reported to have an atypical suppression effect on perceptual priming processes. The aim of this study was to investigate the effects of single doses of lorazepam, diazepam, and a placebo on intrusive memories after exposure to a distressing videotape and to explore whether the anti-intrusive effect of lorazepam is acquired as a result of the suppression of perceptual but not conceptual priming processes. METHODS: Under prospective, randomized, and double-blind conditions, we compared the anti-intrusion effect of a single dose of lorazepam (n=22) with that of diazepam (n=22) and a placebo (n=21) in young healthy Korean college students following exposure to a traumatic videotape. RESULTS: We present the first finding for an anti-intrusion effect of lorazepam. One day after the medication, lorazepam, rather than diazepam or the placebo, significantly reduced the extent of intrusion and data-driven processing of the traumatic information. There were no differences among the three conditions in state anxiety, depression, and an arousal scale throughout the experiment. CONCLUSION: Results from this study suggest the possibility of lorazepam as a candidate anti-intrusion drug, as well as the cautious use of diazepam in the treatment of PTSD patients. The anti-intrusive effect of lorazepam is directly related to its atypical inhibitory effect on implicit perceptual priming processes. The present study provides support for the enhanced perceptual priming hypothesis of PTSD. |
format | Online Article Text |
id | pubmed-3843020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Neuropsychiatric Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-38430202013-12-03 Anti-Intrusion Effect of Lorazepam: An Experimental Study Lee, Hong-Seock Lee, Heung-Pyo Lee, Sang-Kyu Kim, Yong-Ku Choi, Yun-Kyeung Psychiatry Investig Original Article OBJECTIVE: Easy triggering of trauma-related episodic memory fragments caused by perceptual cues is tied to strong perceptual priming in the implicit memory system. And among benzodiazepines, only lorazepam has been consistently reported to have an atypical suppression effect on perceptual priming processes. The aim of this study was to investigate the effects of single doses of lorazepam, diazepam, and a placebo on intrusive memories after exposure to a distressing videotape and to explore whether the anti-intrusive effect of lorazepam is acquired as a result of the suppression of perceptual but not conceptual priming processes. METHODS: Under prospective, randomized, and double-blind conditions, we compared the anti-intrusion effect of a single dose of lorazepam (n=22) with that of diazepam (n=22) and a placebo (n=21) in young healthy Korean college students following exposure to a traumatic videotape. RESULTS: We present the first finding for an anti-intrusion effect of lorazepam. One day after the medication, lorazepam, rather than diazepam or the placebo, significantly reduced the extent of intrusion and data-driven processing of the traumatic information. There were no differences among the three conditions in state anxiety, depression, and an arousal scale throughout the experiment. CONCLUSION: Results from this study suggest the possibility of lorazepam as a candidate anti-intrusion drug, as well as the cautious use of diazepam in the treatment of PTSD patients. The anti-intrusive effect of lorazepam is directly related to its atypical inhibitory effect on implicit perceptual priming processes. The present study provides support for the enhanced perceptual priming hypothesis of PTSD. Korean Neuropsychiatric Association 2013-09 2013-09-16 /pmc/articles/PMC3843020/ /pubmed/24302951 http://dx.doi.org/10.4306/pi.2013.10.3.273 Text en Copyright © 2013 Korean Neuropsychiatric Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Hong-Seock Lee, Heung-Pyo Lee, Sang-Kyu Kim, Yong-Ku Choi, Yun-Kyeung Anti-Intrusion Effect of Lorazepam: An Experimental Study |
title | Anti-Intrusion Effect of Lorazepam: An Experimental Study |
title_full | Anti-Intrusion Effect of Lorazepam: An Experimental Study |
title_fullStr | Anti-Intrusion Effect of Lorazepam: An Experimental Study |
title_full_unstemmed | Anti-Intrusion Effect of Lorazepam: An Experimental Study |
title_short | Anti-Intrusion Effect of Lorazepam: An Experimental Study |
title_sort | anti-intrusion effect of lorazepam: an experimental study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843020/ https://www.ncbi.nlm.nih.gov/pubmed/24302951 http://dx.doi.org/10.4306/pi.2013.10.3.273 |
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