Calipari Erin S, Jones Sara R
Department of Physiology and Pharmacology, Wake Forest School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157, USA.
Department of Physiology and Pharmacology, Wake Forest School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157, USA.
Neuropharmacology. 2014 Jul;82:1-10. doi: 10.1016/j.neuropharm.2014.02.021. Epub 2014 Mar 13.
Long-access methylphenidate (MPH) self-administration has been shown to produce enhanced amphetamine potency at the dopamine transporter and concomitant changes in reinforcing efficacy, suggesting that MPH abuse may change the dopamine system in a way that promotes future drug abuse. While long-access self-administration paradigms have translational validity for cocaine, it may not be as relevant a model of MPH abuse, as it has been suggested that people often take MPH intermittently. Although previous work outlined the neurochemical and behavioral consequences of long-access MPH self-administration, it was not clear whether intermittent access (6 h session; 5 min access/30 min) would result in similar changes. For cocaine, long-access self-administration resulted in tolerance to cocaine's effects on dopamine and behavior while intermittent-access resulted in sensitization. Here we assessed the neurochemical consequences of intermittent-access MPH self-administration on dopamine terminal function. We found increased maximal rates of uptake, increased stimulated release, and subsensitive D2-like autoreceptors. Consistent with previous work using extended-access MPH paradigms, the potencies of amphetamine and MPH, but not cocaine, were increased, demonstrating that unlike cocaine, MPH effects were not altered by the pattern of intake. Although the potency results suggest that MPH may share properties with releasers, dopamine release was increased following acute application of MPH, similar to cocaine, and in contrast to the release decreasing effects of amphetamine. Taken together, these data demonstrate that MPH exhibits properties of both blockers and releasers, and that the compensatory changes produced by MPH self-administration may increase the abuse liability of amphetamines, independent of the pattern of administration.
长期使用甲基苯丙胺(MPH)自我给药已被证明会增强苯丙胺在多巴胺转运体上的效力,并伴随强化效能的变化,这表明MPH滥用可能会以促进未来药物滥用的方式改变多巴胺系统。虽然长期自我给药范式对可卡因具有转化效度,但它可能不是MPH滥用的相关模型,因为有人认为人们经常间歇性地服用MPH。尽管先前的研究概述了长期使用MPH自我给药的神经化学和行为后果,但尚不清楚间歇性给药(6小时时段;5分钟给药/30分钟)是否会导致类似的变化。对于可卡因,长期自我给药导致对可卡因对多巴胺和行为的影响产生耐受性,而间歇性给药则导致敏感化。在这里,我们评估了间歇性使用MPH自我给药对多巴胺终末功能的神经化学后果。我们发现摄取的最大速率增加、刺激释放增加以及D2样自身受体敏感性降低。与先前使用延长使用MPH范式的研究一致,苯丙胺和MPH的效力增加,但可卡因的效力未增加,这表明与可卡因不同,MPH的作用不会因给药模式而改变。尽管效力结果表明MPH可能与释放剂具有共同特性,但与可卡因相似,急性应用MPH后多巴胺释放增加,这与苯丙胺降低释放的作用相反。综上所述,这些数据表明MPH兼具阻断剂和释放剂的特性,并且MPH自我给药产生的代偿性变化可能会增加苯丙胺类药物的滥用倾向,而与给药模式无关。