Watterson Lucas R, Kufahl Peter R, Nemirovsky Natali E, Sewalia Kaveish, Grabenauer Megan, Thomas Brian F, Marusich Julie A, Wegner Scott, Olive M Foster
Department of Psychology, Arizona State University, Tempe, AZ, USA.
Addict Biol. 2014 Mar;19(2):165-74. doi: 10.1111/j.1369-1600.2012.00474.x. Epub 2012 Jul 11.
Reports of abuse and toxic effects of synthetic cathinones, frequently sold as 'bath salts' or 'legal highs', have increased dramatically in recent years. One of the most widely used synthetic cathinones is 3,4-methylenedioxypyrovalerone (MDPV). The current study evaluated the abuse potential of MDPV by assessing its ability to support intravenous self-administration and to lower thresholds for intracranial self-stimulation (ICSS) in rats. In the first experiment, the rats were trained to intravenously self-administer MDPV in daily 2-hour sessions for 10 days at doses of 0.05, 0.1 or 0.2 mg/kg per infusion. The rats were then allowed to self-administer MDPV under a progressive ratio (PR) schedule of reinforcement. Next, the rats self-administered MDPV for an additional 10 days under short access (ShA; 2 hours/day) or long access (LgA; 6 hours/day) conditions to assess escalation of intake. A separate group of rats underwent the same procedures, with the exception of self-administering methamphetamine (0.05 mg/kg per infusion) instead of MDPV. In the second experiment, the effects of MDPV on ICSS thresholds following acute administration (0.1, 0.5, 1 and 2 mg/kg, i.p.) were assessed. MDPV maintained self-administration across all doses tested. A positive relationship between MDPV dose and breakpoints for reinforcement under PR conditions was observed. LgA conditions led to escalation of drug intake at 0.1 and 0.2 mg/kg doses, and rats self-administering methamphetamine showed similar patterns of escalation. Finally, MDPV significantly lowered ICSS thresholds at all doses tested. Together, these findings indicate that MDPV has reinforcing properties and activates brain reward circuitry, suggesting a potential for abuse and addiction in humans.
合成卡西酮通常作为“浴盐”或“合法兴奋剂”出售,近年来,关于其滥用及毒性作用的报告急剧增加。最常用的合成卡西酮之一是3,4-亚甲基二氧吡咯戊酮(MDPV)。本研究通过评估MDPV支持大鼠静脉自我给药的能力以及降低大鼠颅内自我刺激(ICSS)阈值的能力,来评估其滥用潜力。在第一个实验中,训练大鼠在每天2小时的时间段内静脉自我给药MDPV,持续10天,每次输注剂量为0.05、0.1或0.2毫克/千克。然后让大鼠在累进比率(PR)强化程序下自我给药MDPV。接下来,让大鼠在短给药时间(ShA;每天2小时)或长给药时间(LgA;每天6小时)条件下再自我给药MDPV 10天,以评估摄入量的增加情况。另一组大鼠接受相同程序,只是自我给药的是甲基苯丙胺(每次输注0.05毫克/千克)而非MDPV。在第二个实验中,评估了急性给药(腹腔注射0.1、0.5、1和2毫克/千克)后MDPV对ICSS阈值的影响。MDPV在所有测试剂量下均能维持自我给药。在PR条件下,观察到MDPV剂量与强化断点之间呈正相关。LgA条件导致0.1和0.2毫克/千克剂量的药物摄入量增加,且自我给药甲基苯丙胺的大鼠表现出类似的增加模式。最后,MDPV在所有测试剂量下均显著降低了ICSS阈值。这些发现共同表明,MDPV具有强化特性并激活大脑奖赏回路,提示其在人类中有滥用和成瘾的可能性。