Department of Psychology, Center for Studies in Behavioral Neurobiology/FRQS Groupe de recherche en neurobiologie comportementale, Concordia University, Montreal, Quebec, Canada.
Alcohol Clin Exp Res. 2018 Sep;42(9):1795-1806. doi: 10.1111/acer.13825. Epub 2018 Jul 31.
Animal models are critical for studying causal explanations of relapse. Using a Pavlovian conditioning procedure with alcohol, we examined relapse after extinction triggered by either re-exposure to alcohol (reinstatement) or a delay between extinction and test (spontaneous recovery).
Male, Long-Evans rats were acclimated to 15% alcohol in the home-cage using an intermittent-access 2-bottle choice procedure. Next, they received Pavlovian conditioning sessions in which an auditory-conditioned stimulus (CS; 20 second white noise; 8 trials/session; variable time 240 seconds) was paired with 15% alcohol (0.3 ml/CS; 2.4 ml/session) that was delivered into a fluid port for oral ingestion. In subsequent extinction and test sessions, CS presentations occurred as before, but without alcohol.
In experiment 1, exposure to either alcohol or water in the fluid port following extinction reinstated CS-elicited port entries at test 24 hours later. In a follow-up study using the same procedure (experiment 2), reinstatement was more robustly stimulated by alcohol, compared to a familiar lemon-flavored liquid. In experiment 3, systemic alcohol injections (0, 0.5, or 1.0 g/kg, intraperitoneal) administered either 24 hours or 15 minutes before test did not reinstate CS-elicited alcohol-seeking. Importantly, enzymatic assays in experiment 4 revealed detectable levels of alcohol in the blood following oral alcohol intake or intraperitoneal injection, suggesting that a pharmacological effect was likely with either route of administration. Last, in experiment 5, a 23-day delay between extinction and test resulted in a robust spontaneous recovery of CS-elicited alcohol-seeking.
The reinstatement and spontaneous recovery effects revealed herein provide evidence of viable new behavioral paradigms for testing interventions against relapse.
动物模型对于研究复发的因果解释至关重要。我们使用酒精的条件反射程序,检查了由重新暴露于酒精(复吸)或在消退和测试之间的延迟(自发恢复)触发的复发。
雄性长耳兔适应了在笼中使用间歇性接入 2 瓶选择程序摄入 15%酒精。接下来,他们接受了条件反射课程,其中听觉条件刺激(CS;20 秒白噪声;8 次试验/课程;可变时间 240 秒)与 15%酒精(0.3 毫升/CS;2.4 毫升/课程)配对,输送到一个液体端口供口服摄入。在随后的消退和测试课程中,CS 呈现与之前一样,但没有酒精。
在实验 1 中,在消退后暴露于液体端口中的酒精或水会在 24 小时后的测试中重新引发 CS 引发的端口进入。在使用相同程序的后续研究(实验 2)中,与熟悉的柠檬味液体相比,酒精更能强烈刺激复吸。在实验 3 中,在测试前 24 小时或 15 分钟,腹膜内注射 0、0.5 或 1.0 克/千克的系统酒精不会重新引发 CS 引发的酒精寻找。重要的是,在实验 4 中,酶促测定法显示口服酒精摄入或腹膜内注射后血液中可检测到酒精水平,表明无论哪种给药途径都可能产生药理学效应。最后,在实验 5 中,在消退和测试之间的 23 天延迟导致 CS 引发的酒精寻找出现了强烈的自发恢复。
本文所述的复吸和自发恢复效应为测试针对复发的干预措施提供了可行的新行为范式的证据。