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深入探讨酒精引起的 ghrelin 系统变化:来自临床前和临床数据的新见解。

A closer look at alcohol-induced changes in the ghrelin system: novel insights from preclinical and clinical data.

机构信息

Clinical Psychoneuroendocrinology and Neuropsychopharmacology Section, Translational Addiction Medicine Branch, National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Baltimore, Maryland, USA.

Center on Compulsive Behaviors, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Addict Biol. 2022 Jan;27(1):e13033. doi: 10.1111/adb.13033. Epub 2021 Apr 27.

Abstract

Ghrelin is a gastric-derived peptide hormone with demonstrated impact on alcohol intake and craving, but the reverse side of this bidirectional link, that is, the effects of alcohol on the ghrelin system, remains to be fully established. To further characterize this relationship, we examined (1) ghrelin levels via secondary analysis of human laboratory alcohol administration experiments with heavy-drinking participants; (2) expression of ghrelin, ghrelin receptor, and ghrelin-O-acyltransferase (GOAT) genes (GHRL, GHSR, and MBOAT4, respectively) in post-mortem brain tissue from individuals with alcohol use disorder (AUD) versus controls; (3) ghrelin levels in Ghsr knockout and wild-type rats following intraperitoneal (i.p.) alcohol administration; (4) effect of alcohol on ghrelin secretion from gastric mucosa cells ex vivo and GOAT enzymatic activity in vitro; and (5) ghrelin levels in rats following i.p. alcohol administration versus a calorically equivalent non-alcoholic sucrose solution. Acyl- and total-ghrelin levels decreased following acute alcohol administration in humans, but AUD was not associated with changes in central expression of ghrelin system genes in post-mortem tissue. In rats, alcohol decreased acyl-ghrelin, but not des-acyl-ghrelin, in both Ghsr knockout and wild-type rats. No dose-dependent effects of alcohol were observed on acyl-ghrelin secretion from gastric mucosa cells or on GOAT acylation activity. Lastly, alcohol and sucrose produced distinct effects on ghrelin in rats despite equivalent caloric value. Our findings suggest that alcohol acutely decreases peripheral ghrelin concentrations in vivo, but not in proportion to alcohol's caloric value or through direct interaction with ghrelin-secreting gastric mucosal cells, the ghrelin receptor, or the GOAT enzyme.

摘要

胃饥饿素是一种胃来源的肽激素,已被证明对酒精摄入和渴望有影响,但这种双向联系的另一面,即酒精对胃饥饿素系统的影响,仍有待充分确立。为了进一步描述这种关系,我们检查了:(1)通过对重度饮酒参与者进行人体实验室酒精给药实验的二次分析,检测胃饥饿素水平;(2)来自酒精使用障碍(AUD)个体与对照者的死后脑组织中胃饥饿素、胃饥饿素受体和胃饥饿素-O-酰基转移酶(GHRL、GHSR 和 MBOAT4,分别)基因的表达;(3)腹腔内(i.p.)给予酒精后 Ghsr 敲除和野生型大鼠的胃饥饿素水平;(4)酒精对体外胃黏膜细胞中胃饥饿素分泌和 GOAT 酶活性的影响;(5)i.p.给予酒精后大鼠与等热量非酒精性蔗糖溶液相比的胃饥饿素水平。在人类中,急性酒精给药后酰基和总胃饥饿素水平下降,但 AUD 与死后组织中胃饥饿素系统基因的中枢表达变化无关。在大鼠中,酒精降低了 Ghsr 敲除和野生型大鼠的酰基胃饥饿素,但不降低去酰基胃饥饿素。酒精对胃黏膜细胞中酰基胃饥饿素分泌或 GOAT 酰化活性没有剂量依赖性影响。最后,尽管热量值相等,但酒精和蔗糖对大鼠的胃饥饿素产生了不同的影响。我们的研究结果表明,酒精在体内急性降低外周胃饥饿素浓度,但与酒精的热量值不成比例,也不是通过与胃饥饿素分泌胃黏膜细胞、胃饥饿素受体或 GOAT 酶的直接相互作用来实现的。

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