Nikbakhtzadeh Marjan, Borzadaran Fatemeh Mohtashami, Zamani Elham, Shabani Mohammad
Department of Physiology, School of Medicine, Tehran University of Medical Science, Tehran, Iran.
Kerman Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.
Psychiatry Investig. 2020 Jun;17(6):506-516. doi: 10.30773/pi.2020.0002. Epub 2020 Jun 3.
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.
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.
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.
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.
创伤后应激障碍(PTSD)与慢性疼痛常同时出现。研究表明疼痛与PTSD之间存在相互作用。在这篇叙述性综述中,我们旨在通过描述PTSD、疼痛,并确定阿片肽系统及其激动剂和拮抗剂的操控是否会对PTSD症状和并发疼痛产生积极或消极影响,来支持开展全面的研究。
在谷歌学术、Scopus、科学Direct、科学网和PubMed数据库中进行检索词搜索,并对1979年至2019年的关键资源期刊进行手工检索。
在PTSD患者中研究内源性阿片肽系统和阿片肽拮抗剂系统时存在许多矛盾和争议。给PTSD患者外源性给予吗啡可减轻PTSD症状,但对疼痛的减轻作用未达到可接受水平。β-内啡肽作为一种内源性阿片类物质,在事件发生时对减轻疼痛有效,但数分钟至数小时后,内啡肽戒断综合征会导致PTSD的侵入性思维和闪回加剧,从而加重疼痛。研究还表明,阿片肽拮抗剂纳洛酮可减轻或加重PTSD症状及其相关疼痛。
数据表明阿片肽系统及其拮抗剂在PTSD的疼痛控制和情绪方面具有不同作用。然而,需要进一步研究以揭示内源性阿片肽系统和阿片肽拮抗剂系统作为PTSD急性或慢性疼痛患者中介物的作用。