Department of Psychiatry, University of Michigan, Ann Arbor, MI 48109, USA.
Molecules. 2022 Apr 23;27(9):2726. doi: 10.3390/molecules27092726.
Previous studies in animals and humans have shown multiple types of interaction between alcohol (ethanol) intake and the catecholamine signaling molecules: dopamine, norepinephrine and epinephrine. This literature suggests that the administration of alcohol to rodents affects the central and peripheral (blood plasma) levels of these catecholamines. Two prior publications (Fitzgerald 2012, 2020) put forth the hypothesis that there may be a currently unidentified biosynthetic pathway, in a range of organisms, that actually converts alcohol to dopamine, norepinephrine and epinephrine. This publication describes the details for how to test this hypothesis in mice. Mice can be systemically injected with an intoxicating dose of commercially available stable isotope-labeled ethanol (ethanol-1-C), and blood plasma samples and brains can be collected approximately two to 24 h post-injection. Liquid chromatography-mass spectrometry analysis can then be used to test whether some of the labeled ethanol molecules have been incorporated into new dopamine, norepinephrine, and epinephrine molecules, in plasma and brain samples. If confirmed, this hypothesis may have broadly reaching implications both for basic neuroscience and our understanding of alcohol abuse and alcoholism.
先前在动物和人类中的研究表明,酒精(乙醇)摄入与儿茶酚胺信号分子(多巴胺、去甲肾上腺素和肾上腺素)之间存在多种相互作用。这些文献表明,给啮齿动物施用酒精会影响这些儿茶酚胺在中枢和外周(血浆)中的水平。之前有两篇出版物(Fitzgerald,2012,2020)提出了一个假设,即在一系列生物体中,可能存在一种目前尚未识别的生物合成途径,实际上将酒精转化为多巴胺、去甲肾上腺素和肾上腺素。本出版物详细描述了在小鼠中测试该假设的方法。可以给小鼠系统地注射具有致醉作用的商业上可获得的稳定同位素标记的乙醇(乙醇-1-C),并在注射后大约 2 至 24 小时收集血浆样本和大脑。然后可以使用液相色谱-质谱分析来测试标记的乙醇分子中是否有一些已被掺入到新的多巴胺、去甲肾上腺素和肾上腺素分子中,在血浆和大脑样本中。如果得到证实,这个假设可能对基础神经科学以及我们对滥用酒精和酗酒的理解都具有广泛的影响。