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Novel MPDZ/MUPP1 transgenic and knockdown models confirm Mpdz's role in ethanol withdrawal and support its role in voluntary ethanol consumption.新型MPDZ/MUPP1转基因和基因敲低模型证实了Mpdz在乙醇戒断中的作用,并支持其在自愿乙醇消费中的作用。
Addict Biol. 2015 Jan;20(1):143-7. doi: 10.1111/adb.12087. Epub 2013 Oct 10.
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A human laboratory pilot study with baclofen in alcoholic individuals.酒精依赖个体的巴氯芬人体实验室初步研究。
Pharmacol Biochem Behav. 2013 Feb;103(4):784-91. doi: 10.1016/j.pbb.2012.11.013. Epub 2012 Dec 19.
3
Genetic etiology of the common liability to drug dependence: evidence of common and specific mechanisms for DSM-IV dependence symptoms.药物依赖的常见遗传病因:DSM-IV 依赖症状的共同和特定机制证据。
Drug Alcohol Depend. 2012 Jun;123 Suppl 1:S24-32. doi: 10.1016/j.drugalcdep.2011.12.015. Epub 2012 Jan 11.
4
Involvement of nucleus accumbens dopamine D1 receptors in ethanol drinking, ethanol-induced conditioned place preference, and ethanol-induced psychomotor sensitization in mice.伏隔核多巴胺 D1 受体参与小鼠的乙醇摄入、乙醇诱导的条件性位置偏爱和乙醇诱导的运动性敏化。
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Adv Pharmacol. 2011;62:279-314. doi: 10.1016/B978-0-12-385952-5.00003-8.
6
Striatal involvement in human alcoholism and alcohol consumption, and withdrawal in animal models.纹状体在人类酒精中毒和酒精摄入以及动物模型中的戒断中的作用。
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7
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Alcohol Alcohol. 2011 May-Jun;46(3):312-7. doi: 10.1093/alcalc/agr017. Epub 2011 Mar 17.
8
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Behav Brain Res. 2011 Mar 17;218(1):152-7. doi: 10.1016/j.bbr.2010.10.025. Epub 2010 Oct 23.
9
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10
GABAB receptors in reward processes.奖励过程中的GABAB受体。
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黑质网状部尾外侧的Mpdz表达在酒精戒断中起关键作用。

Mpdz expression in the caudolateral substantia nigra pars reticulata is crucially involved in alcohol withdrawal.

作者信息

Kruse L C, Walter N A R, Buck K J

机构信息

Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA; Department of Veterans Affairs Medical Center, Oregon Health & Science University, Portland, OR, USA.

出版信息

Genes Brain Behav. 2014 Nov;13(8):769-76. doi: 10.1111/gbb.12171. Epub 2014 Sep 17.

DOI:10.1111/gbb.12171
PMID:25109596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4241148/
Abstract

Association studies implicate the multiple PDZ domain protein (MUPP1/MPDZ) gene in risk for alcoholism in humans and alcohol withdrawal in mice. Although manipulation of the Mpdz gene by homologous recombination and bacterial artificial chromosome transgenesis has suggested that its expression affects alcohol withdrawal risk, the potential confounding effects of linked genes and developmental compensation currently limit interpretation. Here, using RNA interference (RNAi), we directly test the impact of Mpdz expression on alcohol withdrawal severity and provide brain regional mechanistic information. Lentiviral-mediated delivery of Mpdz short hairpin RNA (shRNA) to the caudolateral substantia nigra pars reticulata (clSNr) significantly reduces Mpdz expression and exacerbates alcohol withdrawal convulsions compared with control mice that delivered a scrambled shRNA. Neither baseline nor pentylenetetrazol-enhanced convulsions differed between Mpdz shRNA and control animals, indicating Mpdz expression in the clSNr does not generally affect seizure susceptibility. To our knowledge, these represent the first in vivo Mpdz RNAi analyses, and provide the first direct evidence that Mpdz expression impacts behavior. Our results confirm that Mpdz is a quantitative trait gene for alcohol withdrawal and demonstrate that its expression in the clSNr is crucially involved in risk for alcohol withdrawal.

摘要

关联研究表明,多PDZ结构域蛋白(MUPP1/MPDZ)基因与人类酒精中毒风险以及小鼠酒精戒断有关。尽管通过同源重组和细菌人工染色体转基因技术对Mpdz基因进行操作表明其表达会影响酒精戒断风险,但目前连锁基因和发育补偿的潜在混杂效应限制了相关解释。在此,我们使用RNA干扰(RNAi)直接测试Mpdz表达对酒精戒断严重程度的影响,并提供脑区机制信息。与递送乱序shRNA的对照小鼠相比,通过慢病毒介导将Mpdz短发夹RNA(shRNA)递送至尾外侧黑质网状部(clSNr)可显著降低Mpdz表达,并加剧酒精戒断惊厥。Mpdz shRNA组和对照组动物的基线惊厥或戊四氮增强惊厥均无差异,这表明clSNr中的Mpdz表达通常不会影响癫痫易感性。据我们所知,这些是首次进行的体内Mpdz RNAi分析,并提供了首个直接证据表明Mpdz表达会影响行为。我们的结果证实Mpdz是酒精戒断的数量性状基因,并表明其在clSNr中的表达与酒精戒断风险密切相关。