Department of Psychiatry and Neurosciences | CCM, Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Germany.
Bernstein Center for Computational Neuroscience Berlin (BCCN), Unter Den Linden 6, 10099, Berlin, Germany.
Psychopharmacology (Berl). 2023 Jan;240(1):171-183. doi: 10.1007/s00213-022-06291-6. Epub 2022 Dec 20.
One hallmark of addiction is an altered neuronal reward processing. In healthy individuals (HC), reduced activity in fronto-striatal regions including the insula has been observed when a reward anticipation task was performed repeatedly. This effect could indicate a desensitization of the neural reward system due to repetition. Here, we investigated this hypothesis in a cohort of patients with alcohol use disorder (AUD), who have been treated with baclofen or a placebo. The efficacy of baclofen in AUD patients has been shown to have positive clinical effects, possibly via indirectly affecting structures within the neuronal reward system.
Twenty-eight recently detoxified patients (13 receiving baclofen (BAC), 15 receiving placebo (PLA)) were investigated within a longitudinal, double-blind, and randomized pharmaco-fMRI design with an individually adjusted daily dosage of 30-270 mg.
Brain responses were captured by functional magnetic resonance imaging (fMRI) during reward anticipation while participating in a slot machine paradigm before (t1) and after 2 weeks of individual high-dose medication (t2).
Abstinence rates were significantly higher in the BAC compared to the PLA group during the 12-week high-dose medication phase. At t1, all patients showed significant bilateral striatal activation. At t2, the BAC group showed a significant decrease in insular activation compared to the PLA group.
By affecting insular information processing, baclofen might enable a more flexible neuronal adaptation during recurrent reward anticipation, which could resemble a desensitization as previously observed in HC. This result strengthens the modulation of the reward system as a potential mechanism of action of baclofen.
Identifier of the main trial (the BACLAD study) at clinical.gov: NCT0126665.
成瘾的一个标志是神经元奖励处理的改变。在健康个体(HC)中,当执行重复的奖励预期任务时,已经观察到包括脑岛在内的额纹状体区域的活动减少。这种效应可能表明由于重复而导致神经奖励系统的脱敏。在这里,我们在一组接受巴氯芬或安慰剂治疗的酒精使用障碍(AUD)患者中研究了这一假设。巴氯芬在 AUD 患者中的疗效已显示出积极的临床效果,可能通过间接影响神经元奖励系统内的结构。
在一项纵向、双盲、随机药物 fMRI 设计中,对 28 名最近戒断的患者(13 名接受巴氯芬(BAC)治疗,15 名接受安慰剂(PLA)治疗)进行了研究,剂量根据个体调整为 30-270mg/天。
通过功能磁共振成像(fMRI)在 slot machine 范式中在奖励预期期间捕获大脑反应,在个体高剂量药物治疗前(t1)和 2 周后(t2)。
在 12 周高剂量药物治疗期间,BAC 组的戒断率明显高于 PLA 组。在 t1,所有患者均显示双侧纹状体激活显著。在 t2,BAC 组的脑岛激活与 PLA 组相比显著降低。
通过影响脑岛的信息处理,巴氯芬可能使在反复奖励预期期间神经元的适应性更加灵活,这可能类似于以前在 HC 中观察到的脱敏。这一结果增强了作为巴氯芬潜在作用机制的奖励系统的调节。
在 clinical.gov 上主要试验(BACLAD 研究)的标识符:NCT0126665。