Hauser Sheketha R, Deehan Gerald A, Knight Christopher P, Toalston Jamie E, McBride William J, Rodd Zachary A
Department of Psychiatry, Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana.
Alcohol Clin Exp Res. 2016 Oct;40(10):2229-2239. doi: 10.1111/acer.13205. Epub 2016 Sep 22.
Drug-paired environments can act as stimuli that elicit drug craving. In humans, drug craving is influenced by the amount of time abstinent, number of past periods of abstinence, and inadvertent exposure to the previously abused drug. The current experiments were designed to determine the effects of (i) the duration of abstinence on expression of ethanol (EtOH)-seeking; (ii) EtOH priming following a short and long abstinence period; and (iii) repeated deprivation cycles on relapse drinking and EtOH-seeking.
Rats were allowed to self-administer 15% EtOH, processed through extinction training, maintained in a home cage for a designated EtOH-free period, and then reintroduced to the operant context in the absence of EtOH. The experiments examined the effects of: (i) various home-cage duration periods (1 to 8 weeks), (ii) priming injections of EtOH in the Pavlovian spontaneous recovery (PSR; 14 days after extinction) and reinstatement of responding (RoR; 1 day after extinction) models, and (iii) exposure to repeated cycles of EtOH access-deprivation on relapse drinking and EtOH-seeking behavior.
Highest expression of EtOH-seeking was observed following 6 weeks of home-cage maintenance. Priming injections of EtOH were more efficacious at stimulating/enhancing EtOH-seeking in the PSR than RoR model. Exposure to repeated cycles of EtOH deprivation and access enhanced and prolonged relapse drinking and the expression of EtOH-seeking (318 ± 22 responses), which was not observed in rats given equivalent consistent exposure to EtOH (66 ± 11 responses).
Overall, the data indicated that the PSR model has ecological validity; factors that enhance EtOH craving in humans enhance the expression of EtOH-seeking in the PSR test. The data also detail factors that need to be examined to determine the biological basis of EtOH-seeking (e.g., neuroadaptations that occur during the incubation period and following repeated cycles of EtOH drinking and abstinence).
与药物配对的环境可作为引发药物渴望的刺激因素。在人类中,药物渴望受禁欲时间长短、过去禁欲次数以及意外接触先前滥用药物的影响。当前的实验旨在确定:(i)禁欲时间对乙醇(EtOH)觅求行为表达的影响;(ii)短期和长期禁欲后乙醇引发效应;(iii)重复剥夺周期对复饮和乙醇觅求行为的影响。
让大鼠自行摄入15%的乙醇,经过消退训练,在无乙醇的指定时间段内饲养于饲养笼中,然后在无乙醇的情况下将其重新引入操作性条件环境。实验考察了以下因素的影响:(i)不同的饲养笼时长(1至8周);(ii)在巴甫洛夫式自发恢复(PSR,消退后14天)和反应恢复(RoR,消退后1天)模型中乙醇引发注射;(iii)暴露于乙醇获取-剥夺的重复周期对复饮和乙醇觅求行为的影响。
饲养笼维持6周后观察到最高水平的乙醇觅求行为表达。在PSR模型中,乙醇引发注射在刺激/增强乙醇觅求行为方面比RoR模型更有效。暴露于乙醇剥夺和获取的重复周期会增强并延长复饮和乙醇觅求行为的表达(318±22次反应),而在持续等量接触乙醇的大鼠中未观察到这种情况(66±11次反应)。
总体而言,数据表明PSR模型具有生态效度;在人类中增强乙醇渴望的因素会增强PSR测试中乙醇觅求行为的表达。数据还详细说明了确定乙醇觅求行为生物学基础所需考察的因素(例如,在潜伏期以及乙醇饮用和禁欲的重复周期后发生的神经适应性变化)。