Valdez Glenn R, Sabino Valentina, Koob George F
Department of Neuropharmacology, The Scripps Research Institute, La Jolla, California, USA.
Alcohol Clin Exp Res. 2004 Jun;28(6):865-72. doi: 10.1097/01.alc.0000128222.29875.40.
Corticotropin-releasing factor (CRF) has been hypothesized to be one of the main regulators of the stress response observed during alcohol withdrawal. The CRF receptor subtypes seem to have a differential role in the regulation of stress-related behavior. Given the behavioral characterization of these receptors, the objective of the following experiments was to characterize the role of CRF2 receptors in the interaction between alcohol and stress by examining the effects of CRF2 receptor activation in the behavioral stress response and ethanol self-administration during early ethanol withdrawal in dependent rats.
Male Wistar rats were made dependent on ethanol via chronic exposure to an ethanol containing liquid diet. Behavior in the elevated plus maze and ethanol self-administration were measured at 2 hr after removal of the diet. The role of the CRF2 receptor in the regulation of these behaviors during the early stages of withdrawal was examined via central injection of the highly selective CRF2 receptor agonist urocortin 3.
Rats showed decreased exploration of the open arms of the elevated plus maze, an indication of a heightened behavioral stress response, after chronic ethanol exposure. This effect was attenuated by central injection of urocortin 3. In addition, urocortin 3 injections reversed the increase in ethanol self-administration observed during early withdrawal in dependent rats.
Reversal of the increased stress-related behavior in the elevated plus maze observed after injections of urocortin 3 indicates that the decreased responding for ethanol also seen after urocortin 3 administration is likely due to a diminished anxiety-like state. These data suggest that activation of the CRF2 receptor may provide a novel target in the attenuation of the stress response characteristic of the early stages of ethanol withdrawal.
促肾上腺皮质激素释放因子(CRF)被认为是酒精戒断期间所观察到的应激反应的主要调节因子之一。CRF受体亚型在应激相关行为的调节中似乎具有不同作用。鉴于这些受体的行为特征,以下实验的目的是通过检测CRF2受体激活对依赖大鼠早期酒精戒断期间行为应激反应和乙醇自我给药的影响,来明确CRF2受体在酒精与应激相互作用中的作用。
雄性Wistar大鼠通过长期暴露于含乙醇的液体饮食而对乙醇产生依赖。在撤除饮食2小时后测量高架十字迷宫中的行为和乙醇自我给药情况。通过脑室内注射高选择性CRF2受体激动剂urocortin 3来研究CRF2受体在戒断早期对这些行为调节中的作用。
长期乙醇暴露后,大鼠在高架十字迷宫开放臂的探索减少,这表明行为应激反应增强。脑室内注射urocortin 3可减弱这种效应。此外,注射urocortin 3可逆转依赖大鼠早期戒断期间观察到的乙醇自我给药增加的情况。
注射urocortin 3后观察到的高架十字迷宫中应激相关行为增加的逆转表明,urocortin 3给药后乙醇反应性降低可能是由于焦虑样状态减轻所致。这些数据表明,激活CRF2受体可能为减轻乙醇戒断早期特征性应激反应提供一个新的靶点。