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Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder
Clonidine and guanfacine are alpha-2 receptor agonists that decrease sympathetic outflow from the central nervous system. Posttraumatic stress disorder (PTSD) is an anxiety disorder that is theorized to be related to a hyperactive sympathetic nervous system. Currently, the only US Food and Drug Admi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Just Medical Media Limited
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544272/ https://www.ncbi.nlm.nih.gov/pubmed/26322115 http://dx.doi.org/10.7573/dic.212286 |
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author | Belkin, Molly R Schwartz, Thomas L |
author_facet | Belkin, Molly R Schwartz, Thomas L |
author_sort | Belkin, Molly R |
collection | PubMed |
description | Clonidine and guanfacine are alpha-2 receptor agonists that decrease sympathetic outflow from the central nervous system. Posttraumatic stress disorder (PTSD) is an anxiety disorder that is theorized to be related to a hyperactive sympathetic nervous system. Currently, the only US Food and Drug Administration (FDA)-approved medications for PTSD are the selective serotonin reuptake inhibitors (SSRIs) sertraline and paroxetine. Sometimes use of the SSRIs may not lead to full remission and symptoms of hyperarousal often persist. This article specifically reviews the literature on alpha-2 receptor agonist use for the treatment of PTSD and concludes that while the evidence base is limited, these agents might be considered useful when SSRIs fail to treat symptoms of agitation and hyperarousal in patients with PTSD. |
format | Online Article Text |
id | pubmed-4544272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Just Medical Media Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-45442722015-08-28 Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder Belkin, Molly R Schwartz, Thomas L Drugs Context Review Clonidine and guanfacine are alpha-2 receptor agonists that decrease sympathetic outflow from the central nervous system. Posttraumatic stress disorder (PTSD) is an anxiety disorder that is theorized to be related to a hyperactive sympathetic nervous system. Currently, the only US Food and Drug Administration (FDA)-approved medications for PTSD are the selective serotonin reuptake inhibitors (SSRIs) sertraline and paroxetine. Sometimes use of the SSRIs may not lead to full remission and symptoms of hyperarousal often persist. This article specifically reviews the literature on alpha-2 receptor agonist use for the treatment of PTSD and concludes that while the evidence base is limited, these agents might be considered useful when SSRIs fail to treat symptoms of agitation and hyperarousal in patients with PTSD. Just Medical Media Limited 2015-08-14 /pmc/articles/PMC4544272/ /pubmed/26322115 http://dx.doi.org/10.7573/dic.212286 Text en Copyright © 2015 Belkin MR, Schwartz TL. Distributed under the terms of the Creative Commons License Deed CC BY 3.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. |
spellingShingle | Review Belkin, Molly R Schwartz, Thomas L Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
title | Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
title_full | Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
title_fullStr | Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
title_full_unstemmed | Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
title_short | Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
title_sort | alpha-2 receptor agonists for the treatment of posttraumatic stress disorder |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544272/ https://www.ncbi.nlm.nih.gov/pubmed/26322115 http://dx.doi.org/10.7573/dic.212286 |
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