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Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction

Behavioral exposure therapy, which involves extinction of the previously acquired fear, has been used to treat anxiety-related symptoms such as post-traumatic stress disorder. It has been hypothesized that proextinction pharmacotherapeutics may enhance the efficacy of exposure therapy. Systemic admi...

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Detalles Bibliográficos
Autores principales: Sethna, Ferzin, Wang, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236415/
https://www.ncbi.nlm.nih.gov/pubmed/25403451
http://dx.doi.org/10.1101/lm.035857.114
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author Sethna, Ferzin
Wang, Hongbing
author_facet Sethna, Ferzin
Wang, Hongbing
author_sort Sethna, Ferzin
collection PubMed
description Behavioral exposure therapy, which involves extinction of the previously acquired fear, has been used to treat anxiety-related symptoms such as post-traumatic stress disorder. It has been hypothesized that proextinction pharmacotherapeutics may enhance the efficacy of exposure therapy. Systemic administration of the metabotropic glutamate receptor 5 (mGluR5)-positive allosteric modulator 3-cyano-N-(1,3-diphenyl-1H-pyrazol-5-yl)benzamide (CDPPB) facilitated the extinction of contextual fear memory. Notably, CDPPB also enhanced the initial fear memory formation, and had no effect on memory retrieval. Our data suggest that positive regulation of mGluR5 may offer a new method to enhance exposure therapy through facilitating extinction without adversely affecting other aspects of memory process.
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spelling pubmed-42364152015-12-01 Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction Sethna, Ferzin Wang, Hongbing Learn Mem Brief Communication Behavioral exposure therapy, which involves extinction of the previously acquired fear, has been used to treat anxiety-related symptoms such as post-traumatic stress disorder. It has been hypothesized that proextinction pharmacotherapeutics may enhance the efficacy of exposure therapy. Systemic administration of the metabotropic glutamate receptor 5 (mGluR5)-positive allosteric modulator 3-cyano-N-(1,3-diphenyl-1H-pyrazol-5-yl)benzamide (CDPPB) facilitated the extinction of contextual fear memory. Notably, CDPPB also enhanced the initial fear memory formation, and had no effect on memory retrieval. Our data suggest that positive regulation of mGluR5 may offer a new method to enhance exposure therapy through facilitating extinction without adversely affecting other aspects of memory process. Cold Spring Harbor Laboratory Press 2014-12 /pmc/articles/PMC4236415/ /pubmed/25403451 http://dx.doi.org/10.1101/lm.035857.114 Text en © 2014 Sethna and Wang; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Brief Communication
Sethna, Ferzin
Wang, Hongbing
Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction
title Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction
title_full Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction
title_fullStr Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction
title_full_unstemmed Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction
title_short Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction
title_sort pharmacological enhancement of mglur5 facilitates contextual fear memory extinction
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236415/
https://www.ncbi.nlm.nih.gov/pubmed/25403451
http://dx.doi.org/10.1101/lm.035857.114
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