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相对流体新奇性以不同方式改变了选择性培育的高酒精偏好小鼠有限获取乙醇和水的摄入时间进程。

Relative fluid novelty differentially alters the time course of limited-access ethanol and water intake in selectively bred high-alcohol-preferring mice.

作者信息

Linsenbardt David N, Boehm Stephen L

机构信息

Addiction Neuroscience, Department of Psychology and Indiana Alcohol Research Center, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana.

出版信息

Alcohol Clin Exp Res. 2015 Apr;39(4):621-30. doi: 10.1111/acer.12679.

Abstract

BACKGROUND

The influence of previous alcohol (ethanol [EtOH])-drinking experience on increasing the rate and amount of future EtOH consumption might be a genetically regulated phenomenon critical to the development and maintenance of repeated excessive EtOH abuse. We have recently found evidence supporting this view, wherein inbred C57BL/6J (B6) mice develop progressive increases in the rate of binge EtOH consumption over repeated drinking-in-the-dark (DID) EtOH access sessions (i.e., "front loading"). The primary goal of this study was to evaluate identical parameters in high-alcohol-preferring (HAP) mice to determine whether similar temporal alterations in limited-access EtOH drinking develop in a population selected for high EtOH preference/intake under continuous (24-hour) access conditions.

METHODS

Using specialized volumetric drinking devices, HAP mice received 14 daily 2-hour DID EtOH or water access sessions. A subset of these mice was then given 1 day access to the opposite assigned fluid on day 15. Home cage locomotor activity was recorded concomitantly on each day of these studies. The possibility of behavioral/metabolic tolerance was evaluated on day 16 using experimenter-administered EtOH.

RESULTS

The amount of EtOH consumed within the first 15 minutes of access increased markedly over days. However, in contrast to previous observations in B6 mice, EtOH front loading was also observed on day 15 in mice that only had previous DID experience with water. Furthermore, a decrease in the amount of water consumed within the first 15 minutes of access compared to animals given repeated water access was observed on day 15 in mice with 14 previous days of EtOH access.

CONCLUSIONS

These data further illustrate the complexity and importance of the temporal aspects of limited-access EtOH consumption and suggest that previous procedural/fluid experience in HAP mice selectively alters the time course of EtOH and water consumption.

摘要

背景

既往饮酒(乙醇[EtOH])经历对未来EtOH摄入量和摄入速度增加的影响可能是一种基因调控现象,这对反复过度EtOH滥用的发生和维持至关重要。我们最近发现了支持这一观点的证据,即近交系C57BL/6J(B6)小鼠在反复进行暗周期饮酒(DID)EtOH摄入实验(即“前期负荷”)过程中,暴饮EtOH的速度会逐渐增加。本研究的主要目的是评估高酒精偏好(HAP)小鼠的相同参数,以确定在持续(24小时)获取条件下,为高EtOH偏好/摄入量选择的群体中,有限获取EtOH饮酒是否会出现类似的时间变化。

方法

使用专门的容积式饮水装置,HAP小鼠每天接受14次为期2小时的DID EtOH或水摄入实验。然后在第15天,让这些小鼠中的一部分接触分配给它们的相反液体1天。在这些研究的每一天,同时记录笼内自发活动。在第16天,使用实验者给予的EtOH评估行为/代谢耐受性的可能性。

结果

在最初15分钟内摄入的EtOH量在数天内显著增加。然而,与之前在B6小鼠中的观察结果相反,在仅曾有过水DID经历的小鼠中,第15天也观察到了EtOH前期负荷现象。此外,在之前有14天EtOH摄入经历的小鼠中,第15天观察到与反复给予水摄入的动物相比,最初15分钟内摄入的水量减少。

结论

这些数据进一步说明了有限获取EtOH饮酒时间方面的复杂性和重要性,并表明HAP小鼠先前的程序/液体经历会选择性地改变EtOH和水摄入的时间进程。

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本文引用的文献

2
Neural and genetic correlates of binge drinking among college women.
Biol Psychol. 2014 Mar;97:43-8. doi: 10.1016/j.biopsycho.2014.01.005. Epub 2014 Feb 14.
3
Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults.
Alcohol Clin Exp Res. 2014 Apr;38(4):930-7. doi: 10.1111/acer.12319. Epub 2014 Jan 15.
4
High drinking in the dark mice: a genetic model of drinking to intoxication.
Alcohol. 2014 May;48(3):217-23. doi: 10.1016/j.alcohol.2013.10.007. Epub 2013 Nov 15.
5
A new scale of the U.S. alcohol policy environment and its relationship to binge drinking.
Am J Prev Med. 2014 Jan;46(1):10-6. doi: 10.1016/j.amepre.2013.07.015.
6
A twin study of genetic influences on diurnal preference and risk for alcohol use outcomes.
J Clin Sleep Med. 2013 Dec 15;9(12):1333-9. doi: 10.5664/jcsm.3282.
7
Alterations in the rate of binge ethanol consumption: implications for preclinical studies in mice.
Addict Biol. 2014 Sep;19(5):812-25. doi: 10.1111/adb.12052. Epub 2013 Mar 13.
8
Selection for drinking in the dark alters brain gene coexpression networks.
Alcohol Clin Exp Res. 2013 Aug;37(8):1295-303. doi: 10.1111/acer.12100. Epub 2013 Mar 29.
9
Role of novelty and ethanol history in locomotor stimulation induced by binge-like ethanol intake.
Alcohol Clin Exp Res. 2012 May;36(5):887-94. doi: 10.1111/j.1530-0277.2011.01684.x. Epub 2011 Dec 7.
10
Pharmacologically relevant intake during chronic, free-choice drinking rhythms in selectively bred high alcohol-preferring mice.
Addict Biol. 2013 Nov;18(6):921-9. doi: 10.1111/j.1369-1600.2011.00412.x. Epub 2011 Nov 29.

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