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A Method for Evaluating the Reinforcing Properties of Ethanol in Rats without Water Deprivation Saccharin Fading or Extended Access Training

机译:一种评估无水缺乏糖精褪色或延长进入训练的大鼠中乙醇的增强特性的方法

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摘要

Operant oral self-administration methods are commonly used to study the reinforcing properties of ethanol in animals. However, the standard methods require saccharin/sucrose fading, water deprivation and/or extended training to initiate operant responding in rats. This paper describes a novel and efficient method to quickly initiate operant responding for ethanol that is convenient for experimenters and does not require water deprivation or saccharin/sucrose fading, thus eliminating the potential confound of using sweeteners in ethanol operant self-administration studies. With this method, Wistar rats typically acquire and maintain self-administration of a 20% ethanol solution in less than two weeks of training. Furthermore, blood ethanol concentrations and rewards are positively correlated for a 30 min self-administration session. Moreover, naltrexone, an FDA-approved medication for alcohol dependence that has been shown to suppress ethanol self-administration in rodents, dose-dependently decreases alcohol intake and motivation to consume alcohol for rats self-administering 20% ethanol, thus validating the use of this new method to study the reinforcing properties of alcohol in rats.
机译:口服操作性自我给药方法通常用于研究动物体内乙醇的增强特性。但是,标准方法需要糖精/蔗糖褪色,缺水和/或扩展训练以启动大鼠的操作员响应。本文介绍了一种新颖,有效的方法,可快速启动乙醇的操作员响应,这对实验人员很方便,并且不需要水分消耗或糖精/蔗糖褪色,从而消除了在乙醇操作员自我管理研究中使用甜味剂的潜在困惑。使用这种方法,Wistar大鼠通常会在不到两周的训练中获得并维持20%乙醇溶液的自我给药。此外,在30分钟的自我管理过程中,血液中的乙醇浓度和回报呈正相关。此外,纳曲酮是一种FDA批准的酒精依赖药物,已被证明能抑制啮齿类动物的乙醇自我施用,它能剂量依赖性地降低酒精摄入量,并能降低大鼠自我施用20%乙醇的饮酒动机,从而验证了纳曲酮的使用有效性。这种新方法研究了酒精对大鼠的增强作用。

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