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Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain
OBJECTIVE: Post-traumatic stress disorder (PTSD) and chronic pain often co-occur. Studies have shown an interaction between pain and PTSD. In this narrative review, we aim to support conducting comprehensive studies by describing PTSD, pain and determining whether opioidergic system, its agonist and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neuropsychiatric Association
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324730/ https://www.ncbi.nlm.nih.gov/pubmed/32492768 http://dx.doi.org/10.30773/pi.2020.0002 |
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author | Nikbakhtzadeh, Marjan Borzadaran, Fatemeh Mohtashami Zamani, Elham Shabani, Mohammad |
author_facet | Nikbakhtzadeh, Marjan Borzadaran, Fatemeh Mohtashami Zamani, Elham Shabani, Mohammad |
author_sort | Nikbakhtzadeh, Marjan |
collection | PubMed |
description | OBJECTIVE: Post-traumatic stress disorder (PTSD) and chronic pain often co-occur. Studies have shown an interaction between pain and PTSD. In this narrative review, we aim to support conducting comprehensive studies by describing PTSD, pain and determining whether opioidergic system, its agonist and antagonist manipulation could positively or negatively affect PTSD symptoms and concurrent pain. METHODS: Term searches was done in Google Scholar, Scopus, ScienceDirect, Web of Science and PubMed databases as well as hand searching in key resource journals from 1979–2019. RESULTS: There are a lot of contradictions and disputes when endogenous opioidergic system and opioidergic antagonist system are studied in PTSD patients. Exogenous morphine administration in PTSD patients can decrease the symptoms of PTSD but it doesn’t have a pain reduction effect to an acceptable level. Beta-endorphin as an endogenous opioid is effective in pain reduction in the moment of events but after minutes to hours, the endorphins withdrawal syndrome leads to exaggerated intrusive thoughts and flashbacks of PTSD, which exacerbate the pain. It has also been shown that naloxone, as an opioidergic antagonist, can reduce or increase the PTSD symptoms and its associated pain. CONCLUSION: Data suggest different roles of opioidergic system and their antagonist in pain control and mood in PTSD. However, further investigations need to be done in order to reveal the role of endogenous opioidergic system and opioidergic antagonist system as a mediator in PTSD patients suffering from acute or chronic pain. |
format | Online Article Text |
id | pubmed-7324730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korean Neuropsychiatric Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-73247302020-07-08 Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain Nikbakhtzadeh, Marjan Borzadaran, Fatemeh Mohtashami Zamani, Elham Shabani, Mohammad Psychiatry Investig Review Article OBJECTIVE: Post-traumatic stress disorder (PTSD) and chronic pain often co-occur. Studies have shown an interaction between pain and PTSD. In this narrative review, we aim to support conducting comprehensive studies by describing PTSD, pain and determining whether opioidergic system, its agonist and antagonist manipulation could positively or negatively affect PTSD symptoms and concurrent pain. METHODS: Term searches was done in Google Scholar, Scopus, ScienceDirect, Web of Science and PubMed databases as well as hand searching in key resource journals from 1979–2019. RESULTS: There are a lot of contradictions and disputes when endogenous opioidergic system and opioidergic antagonist system are studied in PTSD patients. Exogenous morphine administration in PTSD patients can decrease the symptoms of PTSD but it doesn’t have a pain reduction effect to an acceptable level. Beta-endorphin as an endogenous opioid is effective in pain reduction in the moment of events but after minutes to hours, the endorphins withdrawal syndrome leads to exaggerated intrusive thoughts and flashbacks of PTSD, which exacerbate the pain. It has also been shown that naloxone, as an opioidergic antagonist, can reduce or increase the PTSD symptoms and its associated pain. CONCLUSION: Data suggest different roles of opioidergic system and their antagonist in pain control and mood in PTSD. However, further investigations need to be done in order to reveal the role of endogenous opioidergic system and opioidergic antagonist system as a mediator in PTSD patients suffering from acute or chronic pain. Korean Neuropsychiatric Association 2020-06 2020-06-03 /pmc/articles/PMC7324730/ /pubmed/32492768 http://dx.doi.org/10.30773/pi.2020.0002 Text en Copyright © 2020 Korean Neuropsychiatric Association This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Nikbakhtzadeh, Marjan Borzadaran, Fatemeh Mohtashami Zamani, Elham Shabani, Mohammad Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain |
title | Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain |
title_full | Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain |
title_fullStr | Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain |
title_full_unstemmed | Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain |
title_short | Protagonist Role of Opioidergic System on Post-Traumatic Stress Disorder and Associated Pain |
title_sort | protagonist role of opioidergic system on post-traumatic stress disorder and associated pain |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324730/ https://www.ncbi.nlm.nih.gov/pubmed/32492768 http://dx.doi.org/10.30773/pi.2020.0002 |
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