酒精和咖啡因:完美风暴。

Sergi Ferré, Mary Claire O'Brien
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引用次数: 63

摘要

尽管人们普遍认为咖啡因可以对抗酒精的醉人作用,但它们相互作用的分子机制尚不完全清楚。众所周知,咖啡因和酒精都能改变腺苷神经传递,但这种关系很复杂,可能是剂量依赖性的。在这篇文章中,我们回顾了关于咖啡因和酒精结合的现有文献。伦理约束禁止实验室研究模仿许多年轻人在现实环境中达到的高度酒精中毒,无论是否添加咖啡因。我们提出了一种可能的神经化学机制,可以解释在同时摄入咖啡因的人群中观察到的酒精消费量增加和酒精相关后果。咖啡因是一种非选择性腺苷受体拮抗剂。在急性酒精摄入期间,咖啡因通过阻断腺苷A1受体来对抗酒精的“有害”影响,腺苷A1受体介导酒精的促睡眠和共济失调效应。咖啡因的A1受体介导的“不必要的”焦虑效应可能通过酒精诱导的细胞外腺苷浓度的增加而得到改善。此外,通过腺苷A2A和多巴胺D2受体之间的相互作用,咖啡因介导的腺苷A2A受体的阻断可以增强酒精诱导的多巴胺释放的作用。长期饮酒会降低腺苷张力。咖啡因可能通过阻断上调的A1受体的作用,为酒精的戒断效应提供一种“治疗”。最后,咖啡因对A2A受体的阻断可能有助于酒精的强化作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alcohol and Caffeine: The Perfect Storm.

Although it is widely believed that caffeine antagonizes the intoxicating effects of alcohol, the molecular mechanisms underlying their interaction are incompletely understood. It is known that both caffeine and alcohol alter adenosine neurotransmission, but the relationship is complex, and may be dose dependent. In this article, we review the available literature on combining caffeine and alcohol. Ethical constraints prohibit laboratory studies that would mimic the high levels of alcohol intoxication achieved by many young people in real-world settings, with or without the addition of caffeine. We propose a possible neurochemical mechanism for the increase in alcohol consumption and alcohol-related consequences that have been observed in persons who simultaneously consume caffeine. Caffeine is a nonselective adenosine receptor antagonist. During acute alcohol intake, caffeine antagonizes the "unwanted" effects of alcohol by blocking the adenosine A1 receptors that mediate alcohol's somnogenic and ataxic effects. The A1 receptor-mediated "unwanted" anxiogenic effects of caffeine may be ameliorated by alcohol-induced increase in the extracellular concentration of adenosine. Moreover, by means of interactions between adenosine A2A and dopamine D2 receptors, caffeine-mediated blockade of adenosine A2A receptors can potentiate the effects of alcohol-induced dopamine release. Chronic alcohol intake decreases adenosine tone. Caffeine may provide a "treatment" for the withdrawal effects of alcohol by blocking the effects of upregulated A1 receptors. Finally, blockade of A2A receptors by caffeine may contribute to the reinforcing effects of alcohol.

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