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静脉内给予 ghrelin 可增加重度饮酒酒精依赖个体的血清皮质醇和醛固酮浓度:来自双盲、安慰剂对照人体实验室研究的结果。

Intravenous administration of ghrelin increases serum cortisol and aldosterone concentrations in heavy-drinking alcohol-dependent individuals: Results from a double-blind, placebo-controlled human laboratory study.

机构信息

Center for Alcohol and Addiction Studies, Department of Psychiatry and Human Behavior, Brown University, Providence, RI, USA; Center for Alcohol and Addiction Studies, Department of Behavioral and Social Sciences, School of Public Health, Brown University, Providence, RI, 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.

Center for Alcohol and Addiction Studies, Department of Behavioral and Social Sciences, School of Public Health, Brown University, Providence, RI, USA.

出版信息

Neuropharmacology. 2019 Nov 1;158:107711. doi: 10.1016/j.neuropharm.2019.107711. Epub 2019 Jul 13.

Abstract

Increasing evidence supports the role of appetite-regulating hormones, including ghrelin, in alcohol use disorder (AUD). Effects of ghrelin administration on cortisol and aldosterone, two hormones known to influence the development and maintenance of AUD, have been observed in ghrelin-exposed tissues or cells, as well as rodents and healthy volunteers, however whether these effects replicate in individuals with AUD is unknown. Here, we tested the hypothesis that intravenous administration of ghrelin leads to increase in endogenous serum cortisol and aldosterone concentrations in alcohol-dependent, heavy drinking individuals, and that these changes may predict ghrelin-induced alcohol craving. This was a double-blind, placebo-controlled human laboratory study in non-treatment-seeking, heavy-drinking, alcohol-dependent individuals randomized to receive either placebo, 1 mcg/kg or 3 mcg/kg of intravenous ghrelin. Then, participants underwent a cue-reactivity procedure in a bar-like setting, which included exposure to both neutral (juice) and alcohol cues. Repeated blood samples were collected and used to measure endogenous cortisol and aldosterone serum concentrations, in response to exogenous ghrelin administration. Furthermore, cortisol and aldosterone serum concentrations were used to develop a model to predict the effect of exogenous ghrelin administration on alcohol craving. Intravenous ghrelin administration increased endogenous cortisol and aldosterone serum concentrations. While the effects on cortisol were greater than those on aldosterone, only the ghrelin-induced changes in aldosterone serum concentrations predicted craving. These findings provide initial evidence of ghrelin effects on glucocorticoids and mineralocorticoids in individuals with AUD, thereby providing additional information on the potential mechanisms by which the ghrelin system may play a role in alcohol craving and seeking in AUD.

摘要

越来越多的证据表明,食欲调节激素,包括胃饥饿素,在酒精使用障碍(AUD)中发挥作用。在暴露于胃饥饿素的组织或细胞以及啮齿动物和健康志愿者中观察到,胃饥饿素给药对皮质醇和醛固酮的影响,这两种激素已知会影响 AUD 的发展和维持,然而,这些影响是否在 AUD 个体中复制尚不清楚。在这里,我们测试了以下假设:静脉内给予胃饥饿素会导致酒精依赖、大量饮酒个体内源性血清皮质醇和醛固酮浓度增加,并且这些变化可能预测胃饥饿素引起的酒精渴求。这是一项在非治疗寻求、大量饮酒、酒精依赖个体中进行的双盲、安慰剂对照的人体实验室研究,这些个体被随机分配接受安慰剂、1 mcg/kg 或 3 mcg/kg 的静脉内胃饥饿素。然后,参与者在类似于酒吧的环境中进行线索反应程序,包括暴露于中性(果汁)和酒精线索。重复采集血液样本,用于测量内源性皮质醇和醛固酮血清浓度,以响应外源性胃饥饿素给药。此外,皮质醇和醛固酮血清浓度用于开发一种模型,以预测外源性胃饥饿素给药对酒精渴求的影响。静脉内给予胃饥饿素可增加内源性皮质醇和醛固酮血清浓度。虽然皮质醇的作用大于醛固酮,但只有醛固酮血清浓度的胃饥饿素诱导变化预测了渴求。这些发现为 AUD 个体中胃饥饿素对糖皮质激素和盐皮质激素的影响提供了初步证据,从而提供了关于胃饥饿素系统在 AUD 中可能在酒精渴求和寻求中发挥作用的潜在机制的更多信息。

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