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间歇性给予20%乙醇会导致长 Evans 大鼠和 Wistar 大鼠大量饮酒。

Intermittent access to 20% ethanol induces high ethanol consumption in Long-Evans and Wistar rats.

作者信息

Simms Jeffrey A, Steensland Pia, Medina Brian, Abernathy Kenneth E, Chandler L Judson, Wise Roy, Bartlett Selena E

机构信息

Ernest Gallo Clinic and Research Center, University of California San Francisco, Emeryville, California 94608, USA.

出版信息

Alcohol Clin Exp Res. 2008 Oct;32(10):1816-23. doi: 10.1111/j.1530-0277.2008.00753.x. Epub 2008 Jul 30.

Abstract

BACKGROUND

There has been some difficulty getting standard laboratory rats to voluntarily consume large amounts of ethanol without the use of initiation procedures. It has previously been shown that standard laboratory rats will voluntarily consume high levels of ethanol if given intermittent-access to 20% ethanol in a 2-bottle-choice setting [Wise, Psychopharmacologia 29 (1973), 203]. In this study, we have further characterized this drinking model.

METHODS

Ethanol-naïve Long-Evans rats were given intermittent-access to 20% ethanol (three 24-hour sessions per week). No sucrose fading was needed and water was always available ad libitum. Ethanol consumption, preference, and long-term drinking behaviors were investigated. Furthermore, to pharmacologically validate the intermittent-access 20% ethanol drinking paradigm, the efficacy of acamprosate and naltrexone in decreasing ethanol consumption were compared with those of groups given continuous-access to 10 or 20% ethanol, respectively. Additionally, ethanol consumption was investigated in Wistar and out-bred alcohol preferring (P) rats following intermittent-access to 20% ethanol.

RESULTS

The intermittent-access 20% ethanol 2-bottle-choice drinking paradigm led standard laboratory rats to escalate their ethanol intake over the first 5 to 6 drinking sessions, reaching stable baseline consumption of high amounts of ethanol (Long-Evans: 5.1 +/- 0.6; Wistar: 5.8 +/- 0.8 g/kg/24 h, respectively). Furthermore, the cycles of excessive drinking and abstinence led to an increase in ethanol preference and increased efficacy of both acamprosate and naltrexone in Long-Evans rats. P-rats initiate drinking at a higher level than both Long-Evans and Wistar rats using the intermittent-access 20% ethanol paradigm and showed a trend toward a further escalation in ethanol intake over time (mean ethanol intake: 6.3 +/- 0.8 g/kg/24 h).

CONCLUSION

Standard laboratory rats will voluntarily consume ethanol using the intermittent-access 20% ethanol drinking paradigm without the use of any initiation procedures. This model promises to be a valuable tool in the alcohol research field.

摘要

背景

在不采用诱导程序的情况下,让标准实验大鼠自愿大量摄入乙醇存在一定困难。此前研究表明,在双瓶选择环境中给予标准实验大鼠间歇性接触20%乙醇的机会,它们会自愿摄入高水平的乙醇[怀斯,《精神药理学》29(1973),203]。在本研究中,我们进一步对这种饮酒模式进行了特征描述。

方法

对未接触过乙醇的长 Evans 大鼠给予间歇性接触20%乙醇的机会(每周三个24小时时段)。无需蔗糖消退处理,水始终可随意获取。研究了乙醇摄入量、偏好以及长期饮酒行为。此外,为从药理学角度验证间歇性接触20%乙醇的饮酒模式,将阿坎酸和纳曲酮降低乙醇摄入量的效果分别与持续接触10%或20%乙醇的组进行了比较。另外,在给予间歇性接触20%乙醇后,对 Wistar 大鼠和远交系嗜酒(P)大鼠的乙醇摄入量进行了研究。

结果

间歇性接触20%乙醇的双瓶选择饮酒模式使标准实验大鼠在最初的5至6个饮酒时段内乙醇摄入量逐渐增加,达到大量乙醇的稳定基线摄入量(长 Evans 大鼠:5.1±0.6;Wistar 大鼠:5.8±0.8克/千克/24小时)。此外,过量饮酒和戒酒的循环导致长 Evans 大鼠对乙醇的偏好增加,且阿坎酸和纳曲酮的效果增强。使用间歇性接触20%乙醇模式时,P 大鼠开始饮酒的水平高于长 Evans 大鼠和 Wistar 大鼠,且随着时间推移乙醇摄入量有进一步增加的趋势(平均乙醇摄入量:6.3±0.8克/千克/24小时)。

结论

标准实验大鼠使用间歇性接触20%乙醇的饮酒模式可自愿摄入乙醇,无需任何诱导程序。该模型有望成为酒精研究领域的一种有价值的工具。

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本文引用的文献

1
Genetic selection for voluntary alcohol consumption in the albino rat.
Science. 1968 Feb 16;159(3816):739-41. doi: 10.1126/science.159.3816.739.
2
The alcohol-preferring P rat and animal models of excessive alcohol drinking.
Addict Biol. 2006 Sep;11(3-4):270-88. doi: 10.1111/j.1369-1600.2005.00029.x.
3
Intermittent presentations of ethanol sipper tube induce ethanol drinking in rats.
Alcohol Alcohol. 2006 May-Jun;41(3):225-30. doi: 10.1093/alcalc/agl002. Epub 2006 Feb 13.
4
Predictors of acamprosate efficacy: results from a pooled analysis of seven European trials including 1485 alcohol-dependent patients.
Psychopharmacology (Berl). 2005 Mar;178(2-3):167-73. doi: 10.1007/s00213-004-1991-7. Epub 2004 Aug 19.
5
High ethanol preferring rats fail to show dependence following short- or long-term ethanol exposure.
Alcohol Alcohol. 2004 May-Jun;39(3):183-9. doi: 10.1093/alcalc/agh037.
6
The efficacy of acamprosate in the maintenance of abstinence in alcohol-dependent individuals: results of a meta-analysis.
Alcohol Clin Exp Res. 2004 Jan;28(1):51-63. doi: 10.1097/01.ALC.0000108656.81563.05.
7
Dopamine activity in the nucleus accumbens during consummatory phases of oral ethanol self-administration.
Alcohol Clin Exp Res. 2003 Oct;27(10):1573-82. doi: 10.1097/01.ALC.0000089959.66222.B8.
8
Autoshaping of ethanol drinking: an animal model of binge drinking.
Alcohol Alcohol. 2002 Mar-Apr;37(2):138-46. doi: 10.1093/alcalc/37.2.138.

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