Department of Radiology and Biomedical Imaging, Yale University, New Haven, CT 06510, USA.
Department of Psychology, Southern Connecticut State University, New Haven, CT 06515, USA.
Neurosci Biobehav Rev. 2024 Jul;162:105713. doi: 10.1016/j.neubiorev.2024.105713. Epub 2024 May 10.
The kappa opioid receptor (KOR) system is implicated in dysphoria and as an "anti-reward system" during withdrawal from opioids. However, no clear consensus has been made in the field, as mixed findings have been reported regarding the relationship between the KOR system and opioid use. This review summarizes the studies to date on the KOR system and opioids. A systematic scoping review was reported following PRISMA guidelines and conducted based on the published protocol. Comprehensive searches of several databases were done in the following databases: MEDLINE, Embase, PsycINFO, Web of Science, Scopus, and Cochrane. We included preclinical and clinical studies that tested the administration of KOR agonists/antagonists or dynorphin and/or measured dynorphin levels or KOR expression during opioid intoxication or withdrawal from opioids. One hundred studies were included in the final analysis. Preclinical administration of KOR agonists decreased drug-seeking/taking behaviors and opioid withdrawal symptoms. KOR antagonists showed mixed findings, depending on the agent and/or type of withdrawal symptom. Administration of dynorphins attenuated opioid withdrawal symptoms both in preclinical and clinical studies. In the limited number of available studies, dynorphin levels were found to increase in cerebrospinal fluid (CSF) and peripheral blood lymphocytes (PBL) of opioid use disorder subjects (OUD). In animals, dynorphin levels and/or KOR expression showed mixed findings during opioid use. The KOR/dynorphin system appears to have a multifaceted and complex nature rather than simply functioning as an anti-reward system. Future research in well-controlled study settings is necessary to better understand the clinical role of the KOR system in opioid use.
阿片受体 κ 型(KOR)系统与快感缺失有关,并且在阿片类药物戒断期间作为“抗奖赏系统”发挥作用。然而,由于关于 KOR 系统与阿片类药物使用之间的关系,研究结果喜忧参半,因此该领域尚未达成明确共识。本综述总结了迄今为止关于 KOR 系统和阿片类药物的研究。根据发表的方案,按照 PRISMA 指南报告了系统范围的综述,并进行了综述。在以下数据库中进行了全面的数据库搜索:MEDLINE、Embase、PsycINFO、Web of Science、Scopus 和 Cochrane。我们纳入了测试 KOR 激动剂/拮抗剂或强啡肽给药和/或测量阿片类药物中毒或戒断期间强啡肽水平或 KOR 表达的临床前和临床研究。最终分析纳入了 100 项研究。临床前给予 KOR 激动剂可减少觅药/用药行为和阿片类药物戒断症状。KOR 拮抗剂的结果不尽相同,具体取决于药物和/或戒断症状的类型。强啡肽给药可减轻临床前和临床研究中的阿片类药物戒断症状。在为数不多的可用研究中,发现阿片类药物使用障碍(OUD)受试者的脑脊液(CSF)和外周血淋巴细胞(PBL)中的强啡肽水平增加。在动物中,强啡肽水平和/或 KOR 表达在阿片类药物使用期间表现出喜忧参半的结果。KOR/强啡肽系统似乎具有多方面和复杂的性质,而不仅仅是作为抗奖赏系统发挥作用。需要在严格控制的研究环境中进行进一步研究,以更好地了解 KOR 系统在阿片类药物使用中的临床作用。