Galaj Ewa, Newman Amy Hauck, Xi Zheng-Xiong
Molecular Targets and Medication Discovery Branch, National Institute on Drug Abuse, Intramural Research Program, Baltimore, MD, United States.
Molecular Targets and Medication Discovery Branch, National Institute on Drug Abuse, Intramural Research Program, Baltimore, MD, United States.
Neurosci Biobehav Rev. 2020 Jul;114:38-52. doi: 10.1016/j.neubiorev.2020.04.024. Epub 2020 May 3.
Opioid abuse and related overdose deaths continue to rise in the United States, contributing to the current national opioid crisis. Although several opioid-based pharmacotherapies are available (e.g., methadone, buprenorphine, naloxone), they show limited effectiveness in long-term relapse prevention. In response to the opioid crisis, the National Institute on Drug Abuse proposed a list of pharmacological targets of highest priority for medication development for the treatment of opioid use disorders (OUD). Among these are antagonists of dopamine D3 receptors (D3R). In this review, we first review recent progress in research of the dopamine hypothesis of opioid reward and abuse and then describe the rationale and recent development of D3R ligands for the treatment of OUD. Herein, an emphasis is placed on the effectiveness of newly developed D3R antagonists in the animal models of OUD. These new drug candidates may also potentiate the analgesic effects of clinically used opioids, making them attractive as adjunctive medications for pain management and treatment of OUD.
在美国,阿片类药物滥用及相关的过量用药死亡人数持续上升,这加剧了当前全国性的阿片类药物危机。尽管有几种基于阿片类药物的药物疗法(如美沙酮、丁丙诺啡、纳洛酮),但它们在长期预防复发方面效果有限。为应对阿片类药物危机,美国国家药物滥用研究所提出了一份治疗阿片类药物使用障碍(OUD)的药物开发最优先药理学靶点清单。其中包括多巴胺D3受体(D3R)拮抗剂。在本综述中,我们首先回顾阿片类药物奖赏和滥用的多巴胺假说的最新研究进展,然后描述用于治疗OUD的D3R配体的原理及最新进展。在此,重点是新开发的D3R拮抗剂在OUD动物模型中的有效性。这些新的候选药物还可能增强临床使用的阿片类药物的镇痛效果,使其成为疼痛管理和OUD治疗辅助药物的有吸引力的选择。