Crawford Cynthia A, Baella Shelley A, Farley Cristal M, Herbert Matthew S, Horn Leslie R, Campbell Rachel H, Zavala Arturo R
Department of Psychology, California State University, San Bernardino, CA 92407, USA.
Psychopharmacology (Berl). 2011 Jan;213(1):43-52. doi: 10.1007/s00213-010-2011-8. Epub 2010 Sep 17.
Previous studies in rodents show that early exposure to methylphenidate alters later responsiveness to drugs of abuse. An interesting feature of these studies is that early methylphenidate treatment decreases the rewarding value of cocaine when measured by conditioned place preference (CPP), but the same treatment increases cocaine self-administration.
The goal of the present study was to examine the effects of early methylphenidate exposure on cocaine-induced responding using both reward paradigms.
Rats were treated with methylphenidate (0, 2, or 5 mg/kg) from postnatal days (PDs) 11 to 20, and then cocaine-induced CPP or cocaine self-administration was measured in separate groups of rats in adulthood. The CPP procedure included 8 days of acquisition training, 8 days of extinction training, and a reinstatement test. Rats were conditioned with 0, 10, or 20 mg/kg cocaine. Reinstatement was assessed after a priming dose of cocaine (10 mg/kg). For the self-administration experiment, a jugular catheter was implanted and rats were trained to press a lever reinforced with cocaine (0.25 or 0.75 mg/kg/infusion) on a fixed ratio (FR) one schedule. Rats were gradually moved from an FR1 to an FR10 schedule and, after criterion was reached, rats were placed on a progressive ratio schedule for 5 days.
Cocaine produced robust rewarding effects as determined by both the CPP and self-administration experiments; however, early methylphenidate exposure only enhanced the reinforcing effects of cocaine on the self-administration paradigm. Interestingly, this methylphenidate enhancement was only seen in male rats.
These data suggest that in males, methylphenidate enhances the reinforcing value of cocaine, but not cocaine-associated cues.
先前对啮齿动物的研究表明,早期接触哌甲酯会改变后期对滥用药物的反应。这些研究的一个有趣特征是,早期哌甲酯治疗通过条件性位置偏爱(CPP)测量时会降低可卡因的奖赏价值,但相同的治疗会增加可卡因的自我给药量。
本研究的目的是使用两种奖赏范式来研究早期接触哌甲酯对可卡因诱导反应的影响。
从出生后第11天到第20天,用哌甲酯(0、2或5mg/kg)对大鼠进行治疗,然后在成年大鼠的不同组中测量可卡因诱导的CPP或可卡因自我给药量。CPP程序包括8天的习得训练、8天的消退训练和一次恢复测试。用0、10或20mg/kg可卡因对大鼠进行条件化。在给予可卡因启动剂量(10mg/kg)后评估恢复情况。对于自我给药实验,植入颈静脉导管,并训练大鼠在固定比率(FR)为1的时间表上按压用可卡因(0.25或0.75mg/kg/次输注)强化的杠杆。大鼠逐渐从FR1时间表转移到FR10时间表,达到标准后,将大鼠置于渐进比率时间表上5天。
可卡因在CPP和自我给药实验中均产生了强烈的奖赏作用;然而,早期接触哌甲酯仅增强了可卡因在自我给药范式中的强化作用。有趣的是,这种哌甲酯增强作用仅在雄性大鼠中观察到。
这些数据表明,在雄性大鼠中,哌甲酯增强了可卡因的强化价值,但没有增强与可卡因相关的线索。