Oakland University, Dept. of Psychology, 224 Pryale Hall, Rochester, MI 48309, United States.
Oakland University, Dept. of Psychology, Rochester, MI 48309, United States.
Pharmacol Biochem Behav. 2014 Jan;116:16-24. doi: 10.1016/j.pbb.2013.11.020. Epub 2013 Nov 22.
Cues associated with alcohol can stimulate subjective states that increase relapse. Alcohol-cue associations may be strengthened by enhancing adrenergic activity with yohimbine or weakened by blocking adrenergic activity with propranolol. Alcohol-cue associations may also be weakened by long cue exposure sessions or strengthened by short cue exposure sessions. A useful treatment approach for alcoholism may combine adrenergic manipulation with cue exposure sessions of a specific duration. The present study sought to determine if cue exposure during long- or short-duration extinction sessions with post-session yohimbine or propranolol would alter alcohol cue-induced responding and self-administration. Rats were trained to respond for alcohol during sessions that included an olfactory cue given at the beginning of the session and a visual/auditory cue complex delivered concurrently with alcohol. Cue-induced responding was assessed before and after the repeated extinction sessions. Repeated alcohol extinction sessions of long duration (45 min) or short duration (5 min) were followed immediately by injections of saline, yohimbine, or propranolol. After the second set of cue-induced responding tests, reacquisition of operant alcohol self-administration was examined. To determine if the experimental procedures were sensitive to memory manipulation through other pharmacological mechanisms, the NMDA receptor antagonist MK-801 was given 20 min prior to long-duration extinction sessions. Both the long- and short-duration extinction sessions decreased cue-induced responding. Neither yohimbine nor propranolol, given post-session, had subsequent effects on cue-induced responding or alcohol self-administration. MK-801 blocked the effect of extinction sessions on cue-induced responding but had no effect on self-administration. The present study shows that manipulation of the NMDA system in combination with alcohol cue exposure therapy during extinction-like sessions may be more effective than manipulation of the adrenergic system in reducing the strength of alcohol-cue associations in this specific model of alcohol relapse.
与酒精相关的线索可以刺激增加复发的主观状态。通过使用育亨宾增强肾上腺素能活性或使用普萘洛尔阻断肾上腺素能活性,可以增强酒精线索关联。长期线索暴露或短期线索暴露也可以削弱酒精线索关联。酒精成瘾的有效治疗方法可能是将肾上腺素能操作与特定持续时间的线索暴露相结合。本研究旨在确定在长时间或短时间消退期间进行线索暴露,并在消退后给予育亨宾或普萘洛尔,是否会改变酒精线索诱导的反应和自我给药。大鼠在包括在会话开始时给予嗅觉线索和与酒精同时提供的视觉/听觉线索复合物的会话中进行酒精反应训练。在反复消退后,评估线索诱导的反应。长时间(45 分钟)或短时间(5 分钟)的反复酒精消退后,立即给予盐水、育亨宾或普萘洛尔注射。在第二组线索诱导反应测试后,检查操作型酒精自我给药的重新获得。为了确定实验程序是否通过其他药理学机制对记忆操作敏感,在长时间消退后给予 NMDA 受体拮抗剂 MK-801。长时间和短时间消退都会减少线索诱导的反应。无论是在消退后给予的育亨宾还是普萘洛尔,都没有对线索诱导的反应或酒精自我给药产生后续影响。MK-801 阻断了消退对线索诱导反应的影响,但对自我给药没有影响。本研究表明,在类似消退的治疗期间,NMDA 系统的操作与酒精线索暴露治疗相结合,可能比肾上腺素能系统的操作更有效,可降低特定酒精复发模型中酒精线索关联的强度。