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酒精依赖患者的大麻素 CB1 受体结合减少:正电子发射断层扫描研究。

Reduced cannabinoid CB1 receptor binding in alcohol dependence measured with positron emission tomography.

机构信息

Molecular Imaging Branch, National Institute of Mental Health, NIH, Bethesda, MD 20892-1108, USA.

出版信息

Mol Psychiatry. 2013 Aug;18(8):916-21. doi: 10.1038/mp.2012.100. Epub 2012 Jul 10.

Abstract

Brain cannabinoid CB1 receptors contribute to alcohol-related behaviors in experimental animals, but their potential role in humans with alcohol dependence is poorly understood. We measured CB1 receptors in alcohol dependent patients in early and protracted abstinence, and in comparison with control subjects without alcohol use disorders, using positron emission tomography and [(18)F]FMPEP-d2, a radioligand for CB1 receptors. We scanned 18 male in-patients with alcohol dependence twice, within 3-7 days of admission from ongoing drinking, and after 2-4 weeks of supervised abstinence. Imaging data were compared with those from 19 age-matched healthy male control subjects. Data were also analyzed for potential influence of a common functional variation (rs2023239) in the CB1 receptor gene (CNR1) that may moderate CB1 receptor density. On the first scan, CB1 receptor binding was 20-30% lower in patients with alcohol dependence than in control subjects in all brain regions and was negatively correlated with years of alcohol abuse. After 2-4 weeks of abstinence, CB1 receptor binding remained similarly reduced in these patients. Irrespective of the diagnostic status, C allele carriers at rs2023239 had higher CB1 receptor binding compared with non-carriers. Alcohol dependence is associated with a widespread reduction of cannabinoid CB1 receptor binding in the human brain and this reduction persists at least 2-4 weeks into abstinence. The correlation of reduced binding with years of alcohol abuse suggests an involvement of CB1 receptors in alcohol dependence in humans.

摘要

脑内大麻素 CB1 受体参与实验动物的酒精相关行为,但它们在酒精依赖患者中的潜在作用知之甚少。我们使用正电子发射断层扫描和 [(18)F]FMPEP-d2(一种 CB1 受体放射性配体),测量了早期和长期戒酒后的酒精依赖患者以及无酒精使用障碍的对照受试者的 CB1 受体。我们对 18 名男性住院酒精依赖患者进行了两次扫描,一次是在持续饮酒后入院的 3-7 天内,另一次是在经过 2-4 周的监督戒酒之后。将影像学数据与 19 名年龄匹配的健康男性对照受试者的数据进行比较。还分析了 CB1 受体基因 (CNR1) 中常见功能变异(rs2023239)的潜在影响,该变异可能调节 CB1 受体密度。在第一次扫描中,与对照组相比,酒精依赖患者的所有脑区的 CB1 受体结合率降低了 20-30%,且与酒精滥用的年限呈负相关。在 2-4 周的戒酒后,这些患者的 CB1 受体结合仍然类似地降低。无论诊断状态如何,rs2023239 的 C 等位基因携带者的 CB1 受体结合率均高于非携带者。酒精依赖与人类大脑中大麻素 CB1 受体结合的广泛减少有关,这种减少至少在戒酒后 2-4 周内持续存在。与酒精滥用年限的相关性表明 CB1 受体参与了人类的酒精依赖。

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