Preclinical Development Group, Ernest Gallo Clinic and Research Center, 5858 Horton Street, Suite 200, Emeryville, CA, 94608, USA.
Psychopharmacology (Berl). 2011 Nov;218(1):101-10. doi: 10.1007/s00213-011-2451-9. Epub 2011 Aug 24.
Developing models to efficiently explore the mechanisms by which stress can mediate reinstatement of drug-seeking behavior is crucial to the development of new pharmacotherapies for alcohol use disorders.
We examined the effects of multiple reinstatement sessions using the pharmacological stressor, yohimbine, in ethanol- and sucrose-seeking rats in order to develop a more efficient model of stress-induced reinstatement.
Long-Evans rats were trained to self-administer 10% ethanol with a sucrose-fading procedure, 20% ethanol without a sucrose-fading procedure, or 5% sucrose in 30-min operant self-administration sessions, followed by extinction training. After reaching extinction criteria, the animals were tested once per week with yohimbine vehicle and yohimbine (2 mg/kg), respectively, 30 min prior to the reinstatement sessions or blood collection. Levels of reinstatement and plasma corticosterone (CORT) were determined each week for four consecutive weeks.
Yohimbine induced reinstatement of ethanol- and sucrose-seeking in each of the 4 weeks. Interestingly, the magnitude of the reinstatement decreased for the 10% ethanol group after the first reinstatement session but remained stable for the 20% ethanol group trained without sucrose. Plasma CORT levels in response to injection of both vehicle and yohimbine were significantly higher in the ethanol-trained animals compared to sucrose controls.
The stable reinstatement in the 20% ethanol group supports the use of this training procedure in studies using within-subject designs with multiple yohimbine reinstatement test sessions. Additionally, these results indicate that the hormonal response to stressors can be altered following extinction from self-administration of relatively modest amounts of ethanol.
开发能够有效探索压力介导觅药行为复吸机制的模型,对于开发治疗酒精使用障碍的新药物疗法至关重要。
我们使用药理学应激源育亨宾,在乙醇和蔗糖觅药大鼠中检查了多次复吸试验的效果,以便开发一种更有效的应激诱导复吸模型。
长爪沙鼠接受训练,以在 30 分钟的操作性自我给药试验中,分别用 10%乙醇(伴随蔗糖消退程序)、20%乙醇(无蔗糖消退程序)或 5%蔗糖进行自我给药,随后进行消退训练。达到消退标准后,每周用育亨宾载体和育亨宾(2mg/kg)分别测试一次,在复吸试验或采血前 30 分钟进行。连续四周每周确定一次复吸水平和血浆皮质酮(CORT)水平。
育亨宾诱导了每只大鼠在四周内的乙醇和蔗糖觅药复吸。有趣的是,10%乙醇组在第一次复吸试验后,复吸幅度下降,但未接受蔗糖消退程序训练的 20%乙醇组则保持稳定。与蔗糖对照组相比,接受两种载体和育亨宾注射的乙醇训练动物的血浆 CORT 水平显著升高。
20%乙醇组稳定的复吸支持在使用多次育亨宾复吸试验的个体内设计研究中使用这种训练程序。此外,这些结果表明,在从相对少量的乙醇自我给药中消退后,应激源的激素反应可能会发生改变。