Section on Clinical Psychoneuroendocrinology and Neuropsychopharmacology, National Institute on Alcohol Abuse and Alcoholism Division of Intramural Clinical and Biological Research and National Institute on Drug Abuse Intramural Research Program, National Institutes of Health, Bethesda, MD, USA; Center on Compulsive Behaviors, National Institutes of Health, Bethesda, MD, USA.
Section on Clinical Psychoneuroendocrinology and Neuropsychopharmacology, National Institute on Alcohol Abuse and Alcoholism Division of Intramural Clinical and Biological Research and National Institute on Drug Abuse Intramural Research Program, National Institutes of Health, Bethesda, MD, USA.
Physiol Behav. 2019 May 15;204:49-57. doi: 10.1016/j.physbeh.2019.02.008. Epub 2019 Feb 7.
Alcohol use disorder (AUD) is a leading cause of morbidity and mortality worldwide. However, treatment options, including pharmacotherapies, are limited in number and efficacy. Accumulating evidence suggests that elements of the gut-brain axis, such as neuroendocrine pathways and gut microbiome, are involved in the pathophysiology of AUD and, therefore, may be investigated as potential therapeutic targets. One pathway that has begun to be examined in this regard is the ghrelin system. Here, we review preclinical and clinical data on the relationship between ghrelin and alcohol-related outcomes, with a special focus on the role of the ghrelin system as a treatment target for AUD. Observational studies indicate that endogenous ghrelin levels are positively associated with craving for alcohol, subjective responses to alcohol, and brain activity in response to alcohol cues. Knockout rodent models suggest that deletion of the ghrelin peptide or receptor gene leads to reduction of alcohol intake and other alcohol-related outcomes. Different research groups have found that ghrelin administration increases, while ghrelin receptor (GHS-R1a) blockade reduces alcohol intake and other alcohol-related outcomes in rodents. Ghrelin administration in heavy-drinking individuals increases alcohol craving and self-administration and modulates brain activity in response to alcohol reward anticipation. PF-5190457, a GHS-R1a blocker, has been shown to be safe and tolerable when co-administered with alcohol. Furthermore, preliminary results suggest that this compound may reduce cue-elicited craving for alcohol in heavy-drinking individuals - a finding in need of replication. Collectively, the existing literature supports further examination of the ghrelin system as a therapeutic target for AUD. More research is also needed to understand the biobehavioral and molecular mechanisms underlying ghrelin's functions and to examine different interventional approaches to target the ghrelin system for AUD treatment.
酒精使用障碍(AUD)是全球发病率和死亡率的主要原因。然而,治疗选择,包括药物治疗,数量有限,疗效有限。越来越多的证据表明,肠道-大脑轴的元素,如神经内分泌途径和肠道微生物群,参与了 AUD 的病理生理学,因此可以作为潜在的治疗靶点进行研究。在这方面,已经开始研究的一个途径是胃饥饿素系统。在这里,我们综述了胃饥饿素与酒精相关结果之间的关系的临床前和临床数据,特别关注胃饥饿素系统作为 AUD 治疗靶点的作用。观察性研究表明,内源性胃饥饿素水平与对酒精的渴望、对酒精的主观反应以及对酒精线索的大脑活动呈正相关。敲除啮齿动物模型表明,胃饥饿素肽或受体基因的缺失导致酒精摄入量和其他酒精相关结果减少。不同的研究小组发现,胃饥饿素给药增加,而胃饥饿素受体(GHS-R1a)阻断减少酒精摄入量和其他酒精相关结果在啮齿动物。在大量饮酒者中给予胃饥饿素会增加酒精渴望和自我给药,并调节对酒精奖励预期的大脑活动。GHS-R1a 阻断剂 PF-5190457 与酒精同时给药已被证明是安全和耐受的。此外,初步结果表明,这种化合物可能会减少大量饮酒者对酒精的线索诱发的渴望 - 需要复制这一发现。总之,现有文献支持进一步研究胃饥饿素系统作为 AUD 的治疗靶点。还需要更多的研究来了解胃饥饿素功能的生物行为和分子机制,并研究针对 AUD 治疗的不同干预方法来靶向胃饥饿素系统。