Pike Erika, Stoops William W, Rush Craig R
Department of Behavioral Science, University of Kentucky College of Medicine, Medical Behavioral Science Building, Lexington, KY 40536-0086, USA; Department of Psychology, University of Kentucky Arts and Sciences, Kastle Hall, Lexington, KY 40506-0044, USA.
Department of Behavioral Science, University of Kentucky College of Medicine, Medical Behavioral Science Building, Lexington, KY 40536-0086, USA; Department of Psychology, University of Kentucky Arts and Sciences, Kastle Hall, Lexington, KY 40506-0044, USA; Department of Psychiatry, University of Kentucky College of Medicine, 245 Fountain Court, Lexington, KY 40509, USA.
Pharmacol Biochem Behav. 2016 Nov-Dec;150-151:87-93. doi: 10.1016/j.pbb.2016.09.009. Epub 2016 Sep 30.
There is not an approved pharmacotherapy for treating methamphetamine use disorder. This study sought to determine the effects of acute buspirone treatment on the subjective and cardiovascular effects of oral methamphetamine in order to provide an initial assessment of the utility, safety, and tolerability of buspirone for managing methamphetamine use disorder. We predicted that acute buspirone administration would reduce the subjective effects of methamphetamine. We also predicted that the combination of buspirone and methamphetamine would be safe and well tolerated. Ten subjects completed the protocol, which tested three methamphetamine doses (0, 15, and 30mg) in combination with two buspirone doses (0 and 30mg) across 6 experimental sessions. Subjective effects and physiological measures were collected at regular intervals prior to and after dose administration. Methamphetamine produced prototypical subjective and cardiovascular effects. Acute buspirone administration increased some of the abuse-related subjective effects of methamphetamine and also attenuated some cardiovascular effects. The combination of oral methamphetamine and buspirone was safe and well tolerated. Acute buspirone administration may increase the abuse liability of oral methamphetamine. Chronic buspirone dosing studies remain to be conducted, but given preclinical findings and the outcomes of this work, the utility of buspirone for treating methamphetamine use disorder appears limited.
目前尚无获批用于治疗甲基苯丙胺使用障碍的药物疗法。本研究旨在确定急性丁螺环酮治疗对口服甲基苯丙胺的主观及心血管效应的影响,以便对丁螺环酮用于管理甲基苯丙胺使用障碍的效用、安全性和耐受性进行初步评估。我们预测急性给予丁螺环酮会降低甲基苯丙胺的主观效应。我们还预测丁螺环酮与甲基苯丙胺联用将是安全且耐受性良好的。10名受试者完成了该方案,该方案在6个实验环节中测试了三种甲基苯丙胺剂量(0、15和30毫克)与两种丁螺环酮剂量(0和30毫克)的组合。在给药前和给药后的定期时间点收集主观效应和生理指标。甲基苯丙胺产生了典型的主观和心血管效应。急性给予丁螺环酮增加了甲基苯丙胺一些与滥用相关的主观效应,同时也减弱了一些心血管效应。口服甲基苯丙胺与丁螺环酮联用是安全且耐受性良好的。急性给予丁螺环酮可能会增加口服甲基苯丙胺的滥用可能性。丁螺环酮的长期给药研究仍有待开展,但鉴于临床前研究结果及本研究的结果,丁螺环酮用于治疗甲基苯丙胺使用障碍的效用似乎有限。