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α-突触核蛋白的自发缺失与海马和杏仁核中 CB1 mRNA 转录本和受体表达的增加有关:对酒精消费的影响。

A spontaneous deletion of α-synuclein is associated with an increase in CB1 mRNA transcript and receptor expression in the hippocampus and amygdala: effects on alcohol consumption.

机构信息

Department of Psychobiology, Faculty of Psychology, Campus de Somosaguas, Complutense University, 28223 Madrid, Spain.

出版信息

Synapse. 2013 Jun;67(6):280-9. doi: 10.1002/syn.21639. Epub 2013 Mar 20.

DOI:10.1002/syn.21639
PMID:23345080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3931467/
Abstract

α-Synuclein (α-syn) protein and endocannabinoid CB1 receptors are primarily located in presynaptic terminals. An association between α-syn and CB1 receptors has recently been established in Parkinson's disease, but it is completely unknown whether there is an association between these two proteins in alcohol addiction. Therefore, we aimed to examine the α-syn mRNA transcript and protein expression levels in the prefrontal cortex, striatum, amygdala and hippocampus. These brain regions are the most frequently implicated in alcohol and other drug addiction. In these studies, we used C57BL/6 mice carrying a spontaneous deletion of the α-syn gene (C57BL/6(Snca-/-) ) and their respective controls (C57BL/6(Snca) (+/) (+) ). These animals were monitored for spontaneous alcohol consumption (3-10%) and their response to a hypnotic-sedative dose of alcohol (3 g kg(-1) ) was also assessed. Compared with the C57BL/6(Snca+/+) mice, we found that the C57BL/6(Snca-/-) mice exhibited a higher expression level of the CB1 mRNA transcript and CB1 receptor in the hippocampus and amygdala. Furthermore, C57BL/6(Snca-/-) mice showed an increase in alcohol consumption when offered a 10% alcohol solution. There was no significant difference in sleep time after the injection of 3 g/kg alcohol. These results are the first to reveal an association between α-syn and the CB1 receptor in the brain regions that are most frequently implicated in alcohol and other drug addictions.

摘要

α-突触核蛋白(α-syn)和内源性大麻素 CB1 受体主要位于突触前末梢。最近在帕金森病中已经确立了 α-syn 与 CB1 受体之间的关联,但完全未知这两种蛋白质在酒精成瘾中是否存在关联。因此,我们旨在检查前额叶皮层、纹状体、杏仁核和海马体中 α-syn mRNA 转录本和蛋白表达水平。这些大脑区域是最常涉及酒精和其他药物成瘾的区域。在这些研究中,我们使用了携带 α-syn 基因自发缺失的 C57BL/6 小鼠(C57BL/6(Snca-/-))及其各自的对照(C57BL/6(Snca) (+/+))。监测这些动物自发的酒精消费(3-10%),并评估它们对催眠镇静剂量酒精(3 g/kg)的反应。与 C57BL/6(Snca+/+)小鼠相比,我们发现 C57BL/6(Snca-/-)小鼠在海马体和杏仁核中 CB1 mRNA 转录本和 CB1 受体的表达水平更高。此外,当提供 10%酒精溶液时,C57BL/6(Snca-/-)小鼠的酒精消耗量增加。注射 3 g/kg 酒精后睡眠时间没有明显差异。这些结果是首次揭示大脑中与酒精和其他药物成瘾最常涉及的区域中 α-syn 与 CB1 受体之间存在关联。

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本文引用的文献

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Analysis of striatal transcriptome in mice overexpressing human wild-type alpha-synuclein supports synaptic dysfunction and suggests mechanisms of neuroprotection for striatal neurons.分析过度表达人类野生型 α-突触核蛋白的小鼠纹状体转录组支持突触功能障碍,并为纹状体神经元的神经保护提供机制。
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