Breese George R, Chu Kathleen, Dayas Christopher V, Funk Douglas, Knapp Darin J, Koob George F, Lê Dzung Anh, O'Dell Laura E, Overstreet David H, Roberts Amanda J, Sinha Rajita, Valdez Glenn R, Weiss Friedbert
Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599, USA.
Alcohol Clin Exp Res. 2005 Feb;29(2):185-95. doi: 10.1097/01.alc.0000153544.83656.3c.
This report of the proceedings of a symposium presented at the 2004 Research Society on Alcoholism Meeting provides evidence linking stress during sobriety to craving that increases the risk for relapse. The initial presentation by Rajita Sinha summarized clinical evidence for the hypothesis that there is an increased sensitivity to stress-induced craving in alcoholics. During early abstinence, alcoholics who were confronted with stressful circumstances showed increased susceptibility for relapse. George Breese presented data demonstrating that stress could substitute for repeated withdrawals from chronic ethanol to induce anxiety-like behavior. This persistent adaptive change induced by multiple withdrawals allowed stress to induce an anxiety-like response that was absent in animals that were not previously exposed to chronic ethanol. Subsequently, Amanda Roberts reviewed evidence that increased drinking induced by stress was dependent on corticotropin-releasing factor (CRF). In addition, rats that were stressed during protracted abstinence exhibited anxiety-like behavior that was also dependent on CRF. Christopher Dayas indicated that stress increases the reinstatement of an alcohol-related cue. Moreover, this effect was enhanced by previous alcohol dependence. These interactive effects between stress and alcohol-related environmental stimuli depended on concurrent activation of endogenous opioid and CRF systems. A.D. Lê covered information that indicated that stress facilitated reinstatement to alcohol responding and summarized the influence of multiple deprivations on this interaction. David Overstreet provided evidence that restraint stress during repeated alcohol deprivations increases voluntary drinking in alcohol-preferring (P) rats that results in withdrawal-induced anxiety that is not observed in the absence of stress. Testing of drugs on the stress-induced voluntary drinking implicated serotonin and CRF involvement in the sensitized response. Collectively, the presentations provided convincing support for an involvement of stress in the cause of relapse and continuing alcohol abuse and suggested novel pharmacological approaches for treating relapse induced by stress.
这份关于在2004年酒精中毒研究学会会议上举行的研讨会会议记录的报告提供了证据,表明清醒期间的压力与渴望之间存在联系,而这种渴望会增加复发风险。拉吉塔·辛哈的开场发言总结了如下假说的临床证据:酗酒者对应激诱导的渴望更为敏感。在早期戒酒期间,面临压力环境的酗酒者复发的易感性增加。乔治·布里斯展示的数据表明,压力可以替代慢性乙醇反复戒断来诱发类似焦虑的行为。多次戒断所引发的这种持续适应性变化使压力能够诱发一种类似焦虑的反应,而这种反应在之前未接触过慢性乙醇的动物中并不存在。随后,阿曼达·罗伯茨回顾了证据,表明压力导致饮酒增加依赖于促肾上腺皮质激素释放因子(CRF)。此外,在长期戒酒期间受到压力的大鼠表现出的类似焦虑行为也依赖于CRF。克里斯托弗·达亚斯指出,压力会增加与酒精相关线索的恢复。此外,先前的酒精依赖会增强这种效应。压力与酒精相关环境刺激之间的这些相互作用效应取决于内源性阿片类物质和CRF系统的同时激活。A.D.黎介绍了表明压力促进恢复酒精反应的信息,并总结了多次剥夺对这种相互作用的影响。大卫·奥弗斯特里特提供的证据表明,在反复酒精剥夺期间的束缚压力会增加偏爱酒精(P)大鼠的自愿饮酒量,导致戒断引起的焦虑,而在没有压力的情况下则不会观察到这种焦虑。对压力诱导的自愿饮酒进行药物测试表明,5-羟色胺和CRF参与了这种敏感反应。总体而言,这些报告为压力参与复发原因及持续酒精滥用提供了令人信服的支持,并提出了治疗压力诱导复发的新药理学方法。