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2
Derivation and characterization of replicate high- and low-alcohol preferring lines of mice and a high-drinking crossed HAP line.复制的高酒精度和低酒精度偏爱品系小鼠以及高饮酒量杂交 HAP 系的建立和特性研究。
Behav Genet. 2011 Mar;41(2):288-302. doi: 10.1007/s10519-010-9394-5. Epub 2010 Sep 19.
3
The complexity of alcohol drinking: studies in rodent genetic models.酒精摄入的复杂性:啮齿动物遗传模型研究。
Behav Genet. 2010 Nov;40(6):737-50. doi: 10.1007/s10519-010-9371-z. Epub 2010 Jun 15.
4
Schedule of passive ethanol exposure affects subsequent intragastric ethanol self-infusion.被动乙醇暴露时间安排影响随后的胃内乙醇自我输注。
Alcohol Clin Exp Res. 2009 Nov;33(11):1909-23. doi: 10.1111/j.1530-0277.2009.01029.x. Epub 2009 Aug 10.
5
Voluntary ethanol consumption in 22 inbred mouse strains.22个近交系小鼠品系的自愿乙醇摄入量。
Alcohol. 2008 May;42(3):149-60. doi: 10.1016/j.alcohol.2007.12.006. Epub 2008 Mar 20.
6
Acoustic startle at baseline and during acute alcohol withdrawal in replicate mouse lines selectively bred for high or low alcohol preference.在为高酒精偏好或低酒精偏好而选择性培育的复制小鼠品系中,基线时以及急性酒精戒断期间的听觉惊吓反应。
Alcohol Clin Exp Res. 2007 Oct;31(10):1633-44. doi: 10.1111/j.1530-0277.2007.00462.x.
7
Alcohol-related genes: contributions from studies with genetically engineered mice.酒精相关基因:基因工程小鼠研究的贡献
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Toward understanding the genetics of alcohol drinking through transcriptome meta-analysis.通过转录组荟萃分析来理解饮酒的遗传学。
Proc Natl Acad Sci U S A. 2006 Apr 18;103(16):6368-73. doi: 10.1073/pnas.0510188103. Epub 2006 Apr 17.
9
Reestablishing an intragastric ethanol self-infusion model in rats.在大鼠中重建胃内乙醇自我输注模型。
Alcohol Clin Exp Res. 2006 Mar;30(3):414-28. doi: 10.1111/j.1530-0277.2006.00046.x.
10
Alcohol withdrawal severity in inbred mouse (Mus musculus) strains.近交系小鼠(小家鼠)品系中的酒精戒断严重程度。
Behav Neurosci. 2005 Aug;119(4):911-25. doi: 10.1037/0735-7044.119.4.911.

被动乙醇暴露后,高、低饮酒基因型小鼠胃内自我输注乙醇。

Intragastric self-infusion of ethanol in high- and low-drinking mouse genotypes after passive ethanol exposure.

机构信息

Department of Behavioral Neuroscience and Portland Alcohol Research Center, Oregon Health & Science University, Portland, OR 97239-3098, USA.

出版信息

Genes Brain Behav. 2011 Apr;10(3):264-75. doi: 10.1111/j.1601-183X.2010.00664.x. Epub 2010 Dec 16.

DOI:10.1111/j.1601-183X.2010.00664.x
PMID:21091635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3070055/
Abstract

Two experiments examined the effect of 5 days of passive exposure to ethanol (or water) on later self-infusion of ethanol or water via surgically implanted intragastric (IG) catheters in mouse genotypes previously shown to drink high (C57BL/6J, HAP2) or low (DBA/2J, LAP2) amounts of ethanol in home-cage continuous-access two-bottle choice procedures. Intragastric ethanol self-infusion was affected by both genotype and a history of passive ethanol exposure, with greater intakes in the high-drinking genotypes and in groups that received passive exposure to ethanol. Passive ethanol exposure also increased preference for the flavor that signaled ethanol infusion (S+), eliminating genetic differences in this measure. The increases in ethanol intake and S+ preference induced by ethanol exposure might have been mediated jointly by development of tolerance to aversive post-absorptive ethanol effects and negative reinforcement because of alleviation of withdrawal. Bout analyses indicated that ethanol exposure increased ethanol self-infusion by increasing the total number of daily bouts rather than by increasing bout size. These analyses also showed that DBA/2J mice infused larger ethanol bouts and a greater percentage of their total intakes in large bouts than C57BL/6J mice. Overall, these studies suggest that the IG self-infusion procedure is a potentially useful new tool for studying genetic and environmental influences on excessive ethanol intake and preference in mice.

摘要

两项实验研究了 5 天被动暴露于乙醇(或水)对先前通过手术植入胃内(IG)导管进行自我输注乙醇或水的影响,这些小鼠的基因型先前显示在家庭笼连续两瓶选择程序中饮用大量(C57BL/6J、HAP2)或少量(DBA/2J、LAP2)乙醇。IG 内乙醇自我输注受基因型和被动乙醇暴露史的影响,高饮酒基因型和接受被动乙醇暴露的组中摄入量更大。被动乙醇暴露还增加了对提示乙醇输注的味道(S+)的偏好,消除了该措施中遗传差异。乙醇暴露引起的乙醇摄入量增加和 S+偏好可能是由于对吸收后乙醇作用的耐受性发展以及由于缓解戒断而产生的负强化的共同介导。回合分析表明,乙醇暴露通过增加每日总回合数而不是增加回合大小来增加乙醇自我输注。这些分析还表明,DBA/2J 小鼠输注的乙醇回合更大,并且在大回合中占其总摄入量的百分比高于 C57BL/6J 小鼠。总体而言,这些研究表明,IG 自我输注程序是一种研究遗传和环境对小鼠过量乙醇摄入和偏好的潜在有用的新工具。