Centre for Neuropsychopharmacology, Division of Brain Sciences, Imperial College London, London, United Kingdom.
Centre for Neuropsychopharmacology, Division of Brain Sciences, Imperial College London, London, United Kingdom; Department of Psychobiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Biol Psychiatry. 2017 Jun 1;81(11):941-948. doi: 10.1016/j.biopsych.2016.12.029. Epub 2017 Jan 10.
Nalmefene is a µ and δ opioid receptor antagonist, κ opioid receptor partial agonist that has recently been approved in Europe for treating alcohol dependence. It offers a treatment approach for alcohol-dependent individuals with "high-risk drinking levels" to reduce their alcohol consumption. However, the neurobiological mechanism underpinning its effects on alcohol consumption remains to be determined. Using a randomized, double-blind, placebo-controlled, within-subject crossover design we aimed to determine the effect of a single dose of nalmefene on striatal blood oxygen level-dependent (BOLD) signal change during anticipation of monetary reward using the monetary incentive delay task following alcohol challenge.
Twenty-two currently heavy-drinking, non-treatment-seeking alcohol-dependent males were recruited. The effect of single dose nalmefene (18 mg) on changes in a priori defined striatal region of interest BOLD signal change during reward anticipation compared with placebo was investigated using functional magnetic resonance imaging. Both conditions were performed under intravenous alcohol administration (6% vol/vol infusion to achieve a target level of 80 mg/dL).
Datasets from 18 participants were available and showed that in the presence of the alcohol infusion, nalmefene significantly reduced the BOLD response in the striatal region of interest compared with placebo. Nalmefene did not alter brain perfusion.
Nalmefene blunts BOLD response in the mesolimbic system during anticipation of monetary reward and an alcohol infusion. This is consistent with nalmefene's actions on opioid receptors, which modulate the mesolimbic dopaminergic system, and provides a neurobiological basis for its efficacy.
纳美芬是一种μ和δ阿片受体拮抗剂,κ阿片受体部分激动剂,最近在欧洲被批准用于治疗酒精依赖。它为“高风险饮酒水平”的酒精依赖个体提供了一种治疗方法,以减少他们的饮酒量。然而,其对饮酒量影响的神经生物学机制仍有待确定。我们采用随机、双盲、安慰剂对照、自身交叉设计,旨在确定单次纳美芬剂量对酒精挑战后使用金钱奖励延迟任务预测金钱奖励期间纹状体血氧水平依赖(BOLD)信号变化的影响。
招募了 22 名目前重度饮酒、不寻求治疗的酒精依赖男性。使用功能磁共振成像,研究了单次纳美芬(18mg)对酒精输注时预先定义的纹状体感兴趣区 BOLD 信号变化的影响与安慰剂相比的变化。两种情况均在静脉内给予酒精(6%vol/vol 输注,以达到 80mg/dL 的目标水平)。
18 名参与者的数据集可用,结果表明,在酒精输注的情况下,与安慰剂相比,纳美芬显著降低了纹状体感兴趣区的 BOLD 反应。纳美芬并未改变脑灌注。
纳美芬在预期金钱奖励和酒精输注期间减弱了中脑边缘系统的 BOLD 反应。这与纳美芬对阿片受体的作用一致,阿片受体调节中脑边缘多巴胺能系统,并为其疗效提供了神经生物学基础。