Harris Andrew C, Mattson Christina, Shelley David, LeSage Mark G
Minneapolis Medical Research Foundation, Minneapolis, MN, USA; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA; Department of Psychology, University of Minnesota, Minneapolis, MN, USA.
Minneapolis Medical Research Foundation, Minneapolis, MN, USA.
Pharmacol Biochem Behav. 2014 Sep;124:92-100. doi: 10.1016/j.pbb.2014.05.012. Epub 2014 May 24.
Stress enhances the locomotor stimulant and discriminative stimulus effects of several addictive drugs (e.g., morphine) in rodents, yet interactions between stress and nicotine's effects in these behavioral models have not been well established. To this end, the current studies examined the effects of restraint stress on nicotine-induced locomotor activity and nicotine discrimination in rats. We used a novel approach in which onset of stress and nicotine administration occurred concurrently (i.e., simultaneous exposure) to simulate effects of stress on ongoing tobacco use, as well as a more traditional approach in which a delay was imposed between stress and nicotine administration (i.e., sequential exposure). Simultaneous exposure to stress reduced the rate of locomotor sensitization induced by daily injections of nicotine (0.4 mg/kg, s.c.). A lower dose of nicotine (0.1mg/kg, s.c.) produced modest effects on activity that were generally unaffected by simultaneous exposure to stress. Sequential exposure to stress and nicotine (0.4 mg/kg, s.c.) slightly suppressed nicotine-induced activity but did not influence rate of locomotor sensitization. Neither simultaneous nor sequential exposure to stress influenced the discriminative stimulus effects of nicotine (0.01-0.2mg/kg, s.c.). These data show that restraint stress reduces nicotine's locomotor stimulant effects, particularly when onset of stress and nicotine exposure occurs simultaneously, but does not influence nicotine discrimination. These findings contrast with the ability of stress to enhance the effects of other drugs in these models. This study also suggests that studying the influence of simultaneous stress exposure on drug effects may be useful for understanding the role of stress in addiction.
应激可增强啮齿动物中几种成瘾性药物(如吗啡)的运动兴奋和辨别刺激作用,但应激与尼古丁在这些行为模型中的相互作用尚未得到充分证实。为此,本研究考察了束缚应激对大鼠尼古丁诱导的运动活动和尼古丁辨别能力的影响。我们采用了一种新方法,即应激和尼古丁给药同时开始(即同时暴露),以模拟应激对持续吸烟的影响,以及一种更传统的方法,即在应激和尼古丁给药之间设置延迟(即顺序暴露)。同时暴露于应激可降低每日注射尼古丁(0.4mg/kg,皮下注射)诱导的运动敏化率。较低剂量的尼古丁(0.1mg/kg,皮下注射)对活动产生适度影响,一般不受同时暴露于应激的影响。顺序暴露于应激和尼古丁(0.4mg/kg,皮下注射)略微抑制了尼古丁诱导的活动,但不影响运动敏化率。同时或顺序暴露于应激均不影响尼古丁(0.01 - 0.2mg/kg,皮下注射)的辨别刺激作用。这些数据表明,束缚应激可降低尼古丁的运动兴奋作用,尤其是当应激和尼古丁暴露同时开始时,但不影响尼古丁辨别能力。这些发现与应激在这些模型中增强其他药物作用的能力形成对比。本研究还表明,研究同时应激暴露对药物作用的影响可能有助于理解应激在成瘾中的作用。