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创伤应激导致的成瘾易感性:强啡肽/κ阿片受体系统的关键作用。

Traumatic Stress-Induced Vulnerability to Addiction: Critical Role of the Dynorphin/Kappa Opioid Receptor System.

作者信息

Leconte Claire, Mongeau Raymond, Noble Florence

机构信息

Université Paris Cité, INSERM, CNRS, T3S, Paris, France.

出版信息

Front Pharmacol. 2022 Apr 27;13:856672. doi: 10.3389/fphar.2022.856672. eCollection 2022.

Abstract

Substance use disorders (SUD) may emerge from an individual's attempt to limit negative affective states and symptoms linked to stress. Indeed, SUD is highly comorbid with chronic stress, traumatic stress, or post-traumatic stress disorder (PTSD), and treatments approved for each pathology individually often failed to have a therapeutic efficiency in such comorbid patients. The kappa-opioid receptor (KOR) and its endogenous ligand dynorphin (DYN), seem to play a key role in the occurrence of this comorbidity. The DYN/KOR function is increased either in traumatic stress or during drug use, dependence acquisition and DYN is released during stress. The behavioural effects of stress related to the DYN/KOR system include anxiety, dissociative and depressive symptoms, as well as increased conditioned fear response. Furthermore, the DYN/KOR system is implicated in negative reinforcement after the euphoric effects of a drug of abuse ends. During chronic drug consumption DYN/KOR functions increase and facilitate tolerance and dependence. The drug-seeking behaviour induced by KOR activation can be retrieved either during the development of an addictive behaviour, or during relapse after withdrawal. DYN is known to be one of the most powerful negative modulators of dopamine signalling, notably in brain structures implicated in both reward and fear circuitries. KOR are also acting as inhibitory heteroreceptors on serotonin neurons. Moreover, the DYN/KOR system cross-regulate with corticotropin-releasing factor in the brain. The sexual dimorphism of the DYN/KOR system could be the cause of the gender differences observed in patients with SUD or/and traumatic stress-related pathologies. This review underlies experimental and clinical results emphasizing the DYN/KOR system as common mechanisms shared by SUD or/and traumatic stress-related pathologies, and suggests KOR antagonist as a new pharmacological strategy to treat this comorbidity.

摘要

物质使用障碍(SUD)可能源于个体试图限制与压力相关的负面情绪状态和症状。事实上,SUD与慢性应激、创伤性应激或创伤后应激障碍(PTSD)高度共病,针对每种病理单独批准的治疗方法在这类共病患者中往往缺乏治疗效果。κ-阿片受体(KOR)及其内源性配体强啡肽(DYN)似乎在这种共病的发生中起关键作用。DYN/KOR功能在创伤性应激期间或药物使用、成瘾获得过程中增强,且DYN在应激时释放。与DYN/KOR系统相关的应激行为效应包括焦虑、解离和抑郁症状,以及条件性恐惧反应增强。此外,在滥用药物的欣快感结束后,DYN/KOR系统与负性强化有关。在长期药物消费过程中,DYN/KOR功能增强并促进耐受性和依赖性。KOR激活诱导的觅药行为可在成瘾行为发展过程中或戒断后的复发期间出现。已知DYN是多巴胺信号最强大的负性调节因子之一,尤其是在涉及奖赏和恐惧回路的脑结构中。KOR还作为5-羟色胺神经元上的抑制性异源受体发挥作用。此外,DYN/KOR系统在大脑中与促肾上腺皮质激素释放因子相互调节。DYN/KOR系统的性别二态性可能是SUD或/和创伤性应激相关疾病患者中观察到的性别差异的原因。本综述强调了实验和临床结果,突出了DYN/KOR系统是SUD或/和创伤性应激相关疾病共有的共同机制,并提出KOR拮抗剂作为治疗这种共病的一种新药理学策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713a/9091501/8237a3cd2970/fphar-13-856672-g001.jpg

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