Department of Psychology, California State University, Los Angeles, CA 90032, USA.
Neuropsychopharmacology. 2010 Jan;35(2):505-14. doi: 10.1038/npp.2009.155.
A growing body of evidence indicates that protracted use of methamphetamine (mAMPH) causes long-term impairments in cognitive function in humans. Aside from the widely reported problems with attention, mAMPH users exhibit learning and memory deficits, particularly on tasks requiring response control. Although binge mAMPH administration to animals results in cognitive deficits, few studies have attempted to test behavioral flexibility in animals after mAMPH exposure. The aim of this study was to evaluate whether mAMPH would produce impairments in two tasks assessing flexible responding in rats: a touchscreen-based discrimination-reversal learning task and an attentional set shift task (ASST) based on a hallmark test of executive function in humans, the Wisconsin Card Sort. We treated male Long-Evans rats with a regimen of four injections of 2 mg/kg mAMPH (or vehicle) within a single day, a dosing regimen shown earlier to produce object recognition impairments. We then tested them on (1) reversal learning after pretreatment discrimination learning or (2) the ASST. Early reversal learning accuracy was impaired in mAMPH-treated rats. MAMPH pretreatment also selectively impaired reversal performance during ASST testing, leaving set-shifting performance intact. Postmortem analysis of [(125)I]RTI-55 binding revealed small (10-20%) but significant reductions in striatal dopamine transporters produced by this mAMPH regimen. Together, these results lend new information to the growing field documenting impaired cognition after mAMPH exposure, and constitute a rat model of the widely reported decision-making deficits resulting from mAMPH abuse seen in humans.
越来越多的证据表明,长期使用甲基苯丙胺(mAMPH)会导致人类认知功能长期受损。除了广泛报道的注意力问题外,mAMPH 使用者还表现出学习和记忆缺陷,特别是在需要反应控制的任务上。尽管动物 binge 型 mAMPH 给药会导致认知缺陷,但很少有研究试图在 mAMPH 暴露后测试动物的行为灵活性。本研究旨在评估 mAMPH 是否会在两项评估大鼠灵活反应的任务中产生损伤:基于触摸屏的辨别反转学习任务和基于人类执行功能标志性测试威斯康星卡片分类的注意力定势转移任务(ASST)。我们用每天四次 2mg/kg mAMPH(或载体)的方案处理雄性 Long-Evans 大鼠,这一方案以前被证明会导致物体识别障碍。然后,我们在(1)预处理辨别学习后的反转学习或(2)ASST 上测试它们。mAMPH 处理的大鼠在早期反转学习中的准确性受损。mAMPH 预处理还选择性地损害了 ASST 测试中的反转表现,而保留了定势转移表现。[(125)I]RTI-55 结合的死后分析显示,这种 mAMPH 方案导致纹状体多巴胺转运体减少 10-20%,但具有统计学意义。这些结果为越来越多的记录 mAMPH 暴露后认知受损的领域提供了新信息,并构成了一种大鼠模型,该模型模拟了广泛报道的由 mAMPH 滥用导致的人类决策缺陷。