Valdez Glenn R, Roberts Amanda J, Chan Karen, Davis Heather, Brennan Molly, Zorrilla Eric P, Koob George F
Department of Neuropharmacology, The Scripps Research Institute, La Jolla, California 92037, USA.
Alcohol Clin Exp Res. 2002 Oct;26(10):1494-501. doi: 10.1097/01.ALC.0000033120.51856.F0.
Animal models of alcohol dependence suggest that long-term alterations in brain corticotropin-releasing factor (CRF) systems, key mediators of the behavioral stress response, may be involved in the development and reinstatement of dependence on drugs of abuse. The objective of the present study was to investigate the role of CRF in the regulation of ethanol self-administration and to examine the behavioral stress response during acute withdrawal and protracted abstinence.
Male Wistar rats were made dependent on ethanol via chronic exposure to ethanol vapor. Ethanol self-administration and exploratory behavior in the elevated plus maze were measured at 2 hr and 3 to 5 weeks after exposure. The role of CRF in ethanol self-administration was examined via central injection of the CRF receptor antagonist D-Phe-CRF(12-41).
Rats showed increased responding for ethanol 2 hr and 3 to 5 weeks after chronic ethanol exposure, which was attenuated by central injection of D-Phe-CRF(12-41). In addition, rats displayed a decrease in open-arm exploration in the elevated plus maze when tested 2 hr and 4 weeks after exposure.
These results indicate that chronic ethanol exposure leads to increased ethanol self-administration and decreased open-arm exploration in the elevated plus maze during acute withdrawal and protracted abstinence. Attenuation of ethanol self-administration via central injection of D-Phe-CRF(12-41) implicates CRF as an underlying mechanism regulating long-term motivational effects associated with alcohol dependence.
酒精依赖的动物模型表明,大脑促肾上腺皮质激素释放因子(CRF)系统的长期改变,作为行为应激反应的关键调节因子,可能参与了对滥用药物的依赖的发展和复吸过程。本研究的目的是调查CRF在乙醇自我给药调节中的作用,并检查急性戒断和长期禁欲期间的行为应激反应。
雄性Wistar大鼠通过长期暴露于乙醇蒸汽中使其对乙醇产生依赖。在暴露后2小时以及3至5周时测量大鼠在高架十字迷宫中的乙醇自我给药和探索行为。通过向中枢注射CRF受体拮抗剂D-Phe-CRF(12-41)来研究CRF在乙醇自我给药中的作用。
大鼠在慢性乙醇暴露后2小时以及3至5周时对乙醇的反应增加,而向中枢注射D-Phe-CRF(12-41)可使其减弱。此外,在暴露后2小时和4周进行测试时,大鼠在高架十字迷宫中的开臂探索减少。
这些结果表明,慢性乙醇暴露会导致在急性戒断和长期禁欲期间,大鼠在高架十字迷宫中的乙醇自我给药增加,开臂探索减少。通过向中枢注射D-Phe-CRF(12-41)减弱乙醇自我给药表明CRF是调节与酒精依赖相关的长期动机效应的潜在机制。