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Long-term alcohol drinking in High Drinking in the Dark mice is stable for many months and does not show alcohol deprivation effects.长期饮酒在 High Drinking in the Dark 小鼠中稳定持续数月,并不表现出酒精戒断效应。
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本文引用的文献

1
Rodent models of genetic contributions to motivation to abuse alcohol.酒精滥用动机的遗传贡献的啮齿动物模型。
Nebr Symp Motiv. 2014;61:5-29. doi: 10.1007/978-1-4939-0653-6_2.
2
Ethanol Withdrawal-Associated Drinking and Drinking in the Dark: Common and Discrete Genetic Contributions.乙醇戒断相关饮酒与暗中饮酒:共同和离散的遗传贡献
Addict Genet. 2012 Oct 19;1:3-11. doi: 10.2478/addge-2012-0002,.
3
Progress in a replicated selection for elevated blood ethanol concentrations in HDID mice.在 HDID 小鼠中选择提高血液乙醇浓度的重复选择进展。
Genes Brain Behav. 2014 Feb;13(2):236-46. doi: 10.1111/gbb.12105. Epub 2013 Dec 6.
4
Rewarding and aversive effects of ethanol in High Drinking in the Dark selectively bred mice.乙醇对黑暗中高饮酒量选择性培育小鼠的奖赏和厌恶效应。
Addict Biol. 2015 Jan;20(1):80-90. doi: 10.1111/adb.12079. Epub 2013 Jul 30.
5
Cortical activation of accumbens hyperpolarization-active NMDARs mediates aversion-resistant alcohol intake.伏隔核去极化激活型 NMDAR 皮层激活介导了抵抗性酒精摄入。
Nat Neurosci. 2013 Aug;16(8):1094-100. doi: 10.1038/nn.3445. Epub 2013 Jun 30.
6
Ethanol drinking in withdrawal seizure-prone and -resistant selected mouse lines.撤酒发作倾向和抵抗选择的小鼠品系中的乙醇饮用量。
Alcohol. 2013 Aug;47(5):381-9. doi: 10.1016/j.alcohol.2013.05.002.
7
Selection for drinking in the dark alters brain gene coexpression networks.在黑暗中饮水的选择会改变大脑基因共表达网络。
Alcohol Clin Exp Res. 2013 Aug;37(8):1295-303. doi: 10.1111/acer.12100. Epub 2013 Mar 29.
8
Selective breeding for ethanol-related traits alters circadian phenotype.选择性培育与乙醇相关的特征会改变昼夜节律表型。
Alcohol. 2013 May;47(3):187-94. doi: 10.1016/j.alcohol.2013.01.001. Epub 2013 Feb 13.
9
Chronobiology of alcohol: studies in C57BL/6J and DBA/2J inbred mice.酒精的生物钟学:C57BL/6J 和 DBA/2J 近交系小鼠的研究。
Physiol Behav. 2013 Feb 17;110-111:140-7. doi: 10.1016/j.physbeh.2013.01.001. Epub 2013 Jan 10.
10
Escalation of intake under intermittent ethanol access in diverse mouse genotypes.不同小鼠基因型间歇性乙醇摄入的增加。
Addict Biol. 2013 May;18(3):496-507. doi: 10.1111/j.1369-1600.2012.00481.x. Epub 2012 Aug 2.

大量饮酒的暗适应小鼠:一种醉酒的遗传模型。

High drinking in the dark mice: a genetic model of drinking to intoxication.

机构信息

Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR 97239, USA; Portland Alcohol Research Center, VA Medical Center, Portland, OR 97239, USA.

Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR 97239, USA; Portland Alcohol Research Center, VA Medical Center, Portland, OR 97239, USA.

出版信息

Alcohol. 2014 May;48(3):217-23. doi: 10.1016/j.alcohol.2013.10.007. Epub 2013 Nov 15.

DOI:10.1016/j.alcohol.2013.10.007
PMID:24360287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4016107/
Abstract

Drinking to intoxication is a critical component of risky drinking behaviors in humans, such as binge drinking. Previous rodent models of alcohol consumption largely failed to demonstrate that animals were patterning drinking in such a way as to experience intoxication. Therefore, few rodent models of binge-like drinking and no specifically genetic models were available to study possible predisposing genes. The High Drinking in the Dark (HDID) selective breeding project was started to help fill this void, with HDID mice selected for reaching high blood alcohol levels in a limited access procedure. HDID mice now represent a genetic model of drinking to intoxication and can be used to help answer questions regarding predisposition toward this trait as well as potential correlated responses. They should also prove useful for the eventual development of better therapeutic strategies.

摘要

酗酒是人类危险饮酒行为的一个关键组成部分,如狂饮。以前的酒精消费啮齿动物模型在很大程度上未能证明动物的饮酒模式会导致醉酒。因此,很少有类似狂饮的啮齿动物模型,也没有专门的遗传模型来研究可能的易感基因。高饮酒黑暗(HDID)选择育种项目开始启动,以帮助填补这一空白,HDID 小鼠通过有限的接触程序被选择达到高血酒精水平。HDID 小鼠现在代表了一种醉酒的遗传模型,可用于帮助回答有关这种特征的易感性以及潜在的相关反应的问题。它们也应该有助于最终开发更好的治疗策略。