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Ketamine as a prophylactic resilience-enhancing agent

Stress exposure is one of the greatest risk factors for psychiatric illnesses, including major depressive disorder (MDD) and posttraumatic stress disorder (PTSD). Enhancing stress resilience could potentially protect against the development of stress-induced psychiatric disorders, yet no resilience-...

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Autores principales: Evers, Audrey G., Murrough, James W., Charney, Dennis S., Costi, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365980/
https://www.ncbi.nlm.nih.gov/pubmed/35966469
http://dx.doi.org/10.3389/fpsyt.2022.833259
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author Evers, Audrey G.
Murrough, James W.
Charney, Dennis S.
Costi, Sara
author_facet Evers, Audrey G.
Murrough, James W.
Charney, Dennis S.
Costi, Sara
author_sort Evers, Audrey G.
collection PubMed
description Stress exposure is one of the greatest risk factors for psychiatric illnesses, including major depressive disorder (MDD) and posttraumatic stress disorder (PTSD). Enhancing stress resilience could potentially protect against the development of stress-induced psychiatric disorders, yet no resilience-enhancing pharmaceuticals have been developed to date. This review serves to consider the existing evidence for a potential pro-resilience effect of ketamine in rodents as well as the preliminary evidence of ketamine as a prophylactic treatment for postpartum depression (PPD) in humans. Several animal studies have demonstrated that ketamine administered 1 week prior to a stressor (e.g., chronic social defeat and learned helplessness) may protect against depressive-like behavior. A similar protective effect has been demonstrated against PTSD-like behavior following Contextual Fear Conditioning (CFC). Recent work has sought to explore if the administration of ketamine prevented the development of postpartum depression (PPD) in humans. Researchers administered ketamine immediately following caesarian-section and found a significantly reduced prevalence of PPD in the ketamine-treated groups compared to the control groups. Utilizing ketamine as a resilience-enhancing treatment may have unique applications, including leading to a deeper understanding of the neurobiological mechanism underlying resilience. Future trials aiming to translate and replicate these findings with humans are warranted.
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spelling pubmed-93659802022-08-12 Ketamine as a prophylactic resilience-enhancing agent Evers, Audrey G. Murrough, James W. Charney, Dennis S. Costi, Sara Front Psychiatry Psychiatry Stress exposure is one of the greatest risk factors for psychiatric illnesses, including major depressive disorder (MDD) and posttraumatic stress disorder (PTSD). Enhancing stress resilience could potentially protect against the development of stress-induced psychiatric disorders, yet no resilience-enhancing pharmaceuticals have been developed to date. This review serves to consider the existing evidence for a potential pro-resilience effect of ketamine in rodents as well as the preliminary evidence of ketamine as a prophylactic treatment for postpartum depression (PPD) in humans. Several animal studies have demonstrated that ketamine administered 1 week prior to a stressor (e.g., chronic social defeat and learned helplessness) may protect against depressive-like behavior. A similar protective effect has been demonstrated against PTSD-like behavior following Contextual Fear Conditioning (CFC). Recent work has sought to explore if the administration of ketamine prevented the development of postpartum depression (PPD) in humans. Researchers administered ketamine immediately following caesarian-section and found a significantly reduced prevalence of PPD in the ketamine-treated groups compared to the control groups. Utilizing ketamine as a resilience-enhancing treatment may have unique applications, including leading to a deeper understanding of the neurobiological mechanism underlying resilience. Future trials aiming to translate and replicate these findings with humans are warranted. Frontiers Media S.A. 2022-07-28 /pmc/articles/PMC9365980/ /pubmed/35966469 http://dx.doi.org/10.3389/fpsyt.2022.833259 Text en Copyright © 2022 Evers, Murrough, Charney and Costi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Evers, Audrey G.
Murrough, James W.
Charney, Dennis S.
Costi, Sara
Ketamine as a prophylactic resilience-enhancing agent
title Ketamine as a prophylactic resilience-enhancing agent
title_full Ketamine as a prophylactic resilience-enhancing agent
title_fullStr Ketamine as a prophylactic resilience-enhancing agent
title_full_unstemmed Ketamine as a prophylactic resilience-enhancing agent
title_short Ketamine as a prophylactic resilience-enhancing agent
title_sort ketamine as a prophylactic resilience-enhancing agent
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365980/
https://www.ncbi.nlm.nih.gov/pubmed/35966469
http://dx.doi.org/10.3389/fpsyt.2022.833259
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