Merritt Christina R, Garcia Erik J, Brehm Victoria D, Fox Robert G, Moeller F Gerard, Anastasio Noelle C, Cunningham Kathryn A
Center for Addiction Sciences and Therapeutics and Department of Pharmacology and Toxicology, John Sealy School of Medicine, University of Texas Medical Branch, Galveston, TX, United States.
C. Kenneth and Dianne Wright Center for Clinical and Translational Research, Departments of Psychiatry and Pharmacology and Toxicology, Virginia Commonwealth University School of Medicine, Richmond, VA, United States.
Front Pharmacol. 2023 Sep 19;14:1268366. doi: 10.3389/fphar.2023.1268366. eCollection 2023.
The drug overdose crisis has spawned serious health consequences, including the increased incidence of substance use disorders (SUDs), conditions manifested by escalating medical and psychological impairments. While medication management is a key adjunct in SUD treatment, this crisis has crystallized the need to develop additional therapeutics to facilitate extended recovery from SUDs. The "hunger hormone" ghrelin acts by binding to the growth hormone secretagogue receptor 1α (GHS1αR) to control homeostatic and hedonic aspects of food intake and has been implicated in the mechanisms underlying SUDs. Preclinical studies indicate that GHS1αR antagonists and inverse agonists suppress reward-related signaling associated with cocaine and opioids. In the present study, we found that the GHS1αR antagonist JMV2959 was efficacious to suppress both cue-reinforced cocaine and oxycodone drug-seeking, but not cocaine or oxycodone self-administration in male Sprague-Dawley rats. These data suggest a role of the ghrelin-GHS1αR axis in mediating overlapping reward-related aspects of cocaine and oxycodone and premises the possibility that a GHS1αR antagonist may be a valuable therapeutic strategy for relapse vulnerability in SUDs.
药物过量危机已引发了严重的健康后果,包括物质使用障碍(SUDs)的发病率增加,这些病症表现为医学和心理损害的不断升级。虽然药物管理是SUD治疗的关键辅助手段,但这场危机凸显了开发额外治疗方法以促进从SUDs中实现长期康复的必要性。“饥饿激素”胃饥饿素通过与生长激素促分泌素受体1α(GHS1αR)结合来发挥作用,以控制食物摄入的稳态和享乐方面,并与SUDs的潜在机制有关。临床前研究表明,GHS1αR拮抗剂和反向激动剂可抑制与可卡因和阿片类药物相关的奖赏信号。在本研究中,我们发现GHS1αR拮抗剂JMV2959在雄性Sprague-Dawley大鼠中能有效抑制线索强化的可卡因和羟考酮觅药行为,但对可卡因或羟考酮的自我给药无效。这些数据表明胃饥饿素-GHS1αR轴在介导可卡因和羟考酮重叠的奖赏相关方面发挥作用,并提出了GHS1αR拮抗剂可能是治疗SUDs复发易感性的一种有价值的治疗策略的可能性。