Reichel Carmela M, Linkugel Jessica D, Bevins Rick A
Department of Psychology, University of Nebraska Lincoln, Lincoln, NE 68588-0308, USA.
Pharmacol Biochem Behav. 2008 May;89(3):463-72. doi: 10.1016/j.pbb.2008.02.002. Epub 2008 Feb 8.
Bupropion reduces the subjective effects and cue-induced craving for methamphetamine in humans. Given these effects of bupropion on methamphetamine in humans and its widespread clinical use, a preclinical model of drug-taking was used to determine if pretreatment with bupropion would alter the acquisition of methamphetamine self-administration. During acquisition, rats were given saline or bupropion (30 or 60 mg/kg, IP) 5 min before a 60-min session. For the first 8 days, each response on the active lever produced an infusion of methamphetamine (0.025 mg/kg). Responding on the inactive lever had no programmed consequence. This FR1 schedule was then increased to an FR3 for 4 more days. In a parallel study, the identical procedures were used to test the impact of bupropion on sucrose-maintained responding. Bupropion pretreatment decreased the number of methamphetamine infusions and sucrose deliveries earned on an FR1 and FR3. However, bupropion pretreatment only delayed discrimination between the active and inactive levers in the methamphetamine self-administration rats. Discrimination between active and inactive levers was acquired in all groups in the sucrose experiment regardless of pretreatment condition. Combined, these results suggest that bupropion has a more general effect within the appetitive/reward system of the brain rather than having complete specificity for methamphetamine.
安非他酮可减轻人体对甲基苯丙胺的主观效应及线索诱发的渴望。鉴于安非他酮对人体甲基苯丙胺的这些作用及其广泛的临床应用,我们使用了一种药物摄取的临床前模型来确定安非他酮预处理是否会改变甲基苯丙胺自我给药的习得过程。在习得过程中,大鼠在60分钟实验前5分钟给予生理盐水或安非他酮(30或60毫克/千克,腹腔注射)。在最初的8天里,主动杆上的每次反应都会导致注入甲基苯丙胺(0.025毫克/千克)。在非主动杆上的反应没有设定的结果。然后,这种固定比率1(FR1)程序在接下来的4天增加到固定比率3(FR3)。在一项平行研究中,采用相同的程序来测试安非他酮对蔗糖维持反应的影响。安非他酮预处理减少了在FR1和FR3上获得的甲基苯丙胺注入量和蔗糖递送量。然而,安非他酮预处理仅延迟了甲基苯丙胺自我给药大鼠对主动杆和非主动杆的辨别。在蔗糖实验中,无论预处理条件如何,所有组都获得了对主动杆和非主动杆的辨别。综合来看,这些结果表明安非他酮在大脑的食欲/奖励系统中具有更广泛的作用,而不是对甲基苯丙胺具有完全的特异性。