Stafford Alexandra M, Anderson Shawn M, Shelton Keith L, Brunzell Darlene H
Department of Pharmacology and Toxicology, Virginia Commonwealth University, 410 N 12th St., Richmond, VA, 23298, USA.
Psychopharmacology (Berl). 2015 Oct;232(20):3783-95. doi: 10.1007/s00213-015-4040-9. Epub 2015 Aug 14.
Mouse models of ethanol (EtOH) self-administration are useful to identify genetic and biological underpinnings of alcohol use disorder.
These experiments developed a novel method of oral operant EtOH self-administration in mice without explicitly paired cues, food/water restriction, or EtOH fading.
Following magazine and lever training for 0.2 % saccharin (SAC), mice underwent nine weekly overnight sessions with lever pressing maintained by dipper presentation of 0, 3, 10, or 15 % EtOH in SAC or water vehicle. Ad libitum water was available from a bottle.
Water vehicle mice ingested most fluid from the water bottle in contrast to SAC vehicle mice, which despite lever pressing demands, drank most of their fluid from the liquid dipper. Although EtOH in SAC vehicle mice showed concentration-dependent increases of g/kg EtOH intake, lever pressing decreased with increasing EtOH concentration and did not exceed that of SAC vehicle alone at any EtOH concentration. Mice reinforced with EtOH in water ingested less EtOH than mice reinforced with EtOH in SAC. EtOH in water mice, however, showed concentration-dependent increases in g/kg EtOH intake and lever presses. Fifteen percent EtOH in water mice showed significantly greater levels of lever pressing than water vehicle mice and a significant escalation of responding across weeks of exposure. Naltrexone pretreatment reduced EtOH self-administration and intake in these mice without altering responding in the vehicle control condition during the first hour of the session.
SAC facilitated EtOH intake but prevented observation of EtOH reinforcement. Water vehicle unmasked EtOH's reinforcing effects.
乙醇(EtOH)自我给药的小鼠模型有助于识别酒精使用障碍的遗传和生物学基础。
这些实验开发了一种在小鼠中进行口服操作性EtOH自我给药的新方法,无需明确配对线索、食物/水限制或EtOH逐渐减量。
在对0.2%糖精(SAC)进行食盒和杠杆训练后,小鼠进行了为期九周的每周夜间实验,通过在SAC或水载体中以0、3、10或15%的EtOH进行勺喂来维持杠杆按压。可从瓶中自由获取水。
与SAC载体小鼠相比,水载体小鼠从水瓶中摄入的液体最多,尽管有杠杆按压需求,SAC载体小鼠大部分液体是从液体勺中饮用的。尽管SAC载体小鼠中的EtOH显示出按克/千克EtOH摄入量的浓度依赖性增加,但随着EtOH浓度的增加,杠杆按压减少,在任何EtOH浓度下都未超过单独SAC载体小鼠的水平。用水中EtOH强化的小鼠比用SAC中EtOH强化的小鼠摄入的EtOH少。然而,水中EtOH小鼠按克/千克EtOH摄入量和杠杆按压显示出浓度依赖性增加。水中15%EtOH小鼠的杠杆按压水平明显高于水载体小鼠,并且在暴露的几周内反应有显著增加。纳曲酮预处理减少了这些小鼠的EtOH自我给药和摄入量,而在实验的第一个小时内未改变载体对照条件下的反应。
SAC促进了EtOH摄入,但阻止了对EtOH强化的观察。水载体揭示了EtOH的强化作用。