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Reduced Cannabinoid CB1 Receptor Binding in Alcohol Dependence Measured with Positron Emission Tomographys

机译:用正电子发射断层图像测量的醇依赖性减少大麻素CB1受体结合

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摘要

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 (PET) and [18F]FMPEP-d2, a radioligand for CB1 receptors. We scanned 18 male inpatients 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 diagnostic status, C allele carriers at rs2023239 had higher CB1 receptor binding compared to 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.
机译:脑大麻素CB1受体有助于实验动物中与酒精有关的行为,但人们对它们在酒精依赖者中的潜在作用了解甚少。我们使用正电子发射断层扫描(PET)和[ 18 F] FMPEP-d2(一种放射性配体),在酒精依赖患者的早期和长期禁欲中测量了CB1受体,并与无酒精使用障碍的对照受试者进行了比较。用于CB1受体。我们对18名患有酒精依赖的男性住院患者进行了两次扫描,两次扫描是在持续饮酒后的3至7天内,以及在监督禁酒的2至4周后进行的。将成像数据与来自19个年龄相匹配的健康男性对照组的数据进行了比较。还分析了数据对可能调节CB1受体密度的CB1受体基因(CNR1)中常见功能变异(rs2023239)的潜在影响。第一次扫描时,酒精依赖患者的CB1受体结合率在所有脑区域均比对照组低20%至30%,并且与多年酗酒呈负相关。禁欲2到4周后,这些患者的CB1受体结合仍然相似地降低。无论诊断状态如何,rs2023239的C等位基因携带者与非携带者相比具有更高的CB1受体结合。酒精依赖与大麻素CB1受体在人脑中的结合广泛减少有关,这种减少持续至少2-4周。结合减少与酗酒年限的相关性表明,CB1受体参与了人类的酒精依赖。

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