Department of Psychiatry at New York State Psychiatric Institute and Columbia University, New York, New York 10032, USA.
Biol Psychiatry. 2010 Oct 15;68(8):689-96. doi: 10.1016/j.biopsych.2010.06.005. Epub 2010 Aug 3.
We used a positron emission tomography paradigm with the D2/3 radiotracer [¹¹C]raclopride and an alcohol challenge to examine the magnitude of alcohol-induced dopamine release and compare it between young men and women.
Twenty-one nonalcohol-dependent young social drinkers completed two positron emission tomography scans on separate days following ingestion of a juice mix containing either ethanol (.75 mg/kg body water) or trace ethanol only. The extent of dopamine released after alcohol was estimated by the percentage difference in [¹¹C]raclopride binding potential (ΔBP(ND)) between days.
Alcohol administration significantly displaced [¹¹C]raclopride in all striatal subregions, indicating dopamine release, with the largest effect observed in the ventral striatum. Linear mixed model analysis across all striatal subregions of regional ΔBP(ND) with region of interest as repeated measure showed a highly significant effect of sex (p < .001). Ventrostriatal dopamine release in men, but not in women, showed a significant positive correlation to alcohol-induced measures of subjective activation. Furthermore, we found a significant negative correlation between the frequency of maximum alcohol consumption per 24 hours and ventrostriatal ΔBP(ND) (r = .739, p = .009) in men.
This study provides definitive evidence that oral alcohol induces dopamine release in nonalcoholic human subjects and shows sex differences in the magnitude of this effect. The ability of alcohol to stimulate dopamine release may contribute to its rewarding effects and, thereby, to its abuse liability in humans. Our report further suggests several biological mechanisms that may mediate the difference in vulnerability for alcoholism between men and women.
我们使用正电子发射断层扫描范式,使用 D2/3 放射性示踪剂 [¹¹C]raclopride 和酒精挑战来检查酒精诱导的多巴胺释放的程度,并在男性和女性之间进行比较。
21 名非酒精依赖的年轻社交饮酒者在分别服用含有乙醇(0.75 毫克/千克体重水)或仅痕量乙醇的果汁混合物后的两天内完成了两次正电子发射断层扫描。通过 [¹¹C]raclopride 结合潜力(ΔBP(ND))在两天之间的差异百分比来估计酒精后多巴胺的释放程度。
酒精给药显著置换了所有纹状体亚区中的 [¹¹C]raclopride,表明多巴胺释放,在腹侧纹状体中观察到最大效应。对所有纹状体亚区的区域 ΔBP(ND)进行线性混合模型分析,以感兴趣区域为重复测量,显示出性别(p<.001)的高度显著影响。男性的腹侧纹状体多巴胺释放,但女性没有,与酒精引起的主观激活测量呈显著正相关。此外,我们发现男性的最大饮酒量(每 24 小时)与腹侧纹状体 ΔBP(ND)之间存在显著负相关(r = -.739,p =.009)。
这项研究提供了确凿的证据,表明口服酒精会在非酒精性人类受试者中诱导多巴胺释放,并显示出这种效应的性别差异。酒精刺激多巴胺释放的能力可能与其奖赏作用有关,从而与其在人类中的滥用倾向有关。我们的报告进一步提出了几种可能介导男性和女性之间对酒精中毒易感性差异的生物学机制。