Sharpe L G, Jaffe J H, Katz J L
Psychobiology Laboratory, Baltimore, Maryland 21224.
Life Sci. 1992;51(3):PL13-8. doi: 10.1016/0024-3205(92)90081-y.
Anecdotal evidence in humans suggest that carbamazepine suppresses cocaine-induced rush and craving. Such claims are unsupported in controlled trials using a placebo control. In the present study, rats were trained to self-administer i.v. cocaine in daily 2-hr sessions in which every tenth lever press delivered 1 mg/kg cocaine. After responding was stable, they were injected before each session with the vehicle for 2 days followed by carbamazepine for 2 days. At a 7 mg/kg dose, carbamazepine was without effect, whereas 15 mg/kg suppressed responding for cocaine only on the second (day 4) day of carbamazepine treatment. With 4 consecutive days of treatment, carbamazepine (15 mg/kg) reduced cocaine-maintained responding slightly, but significantly. In another group of animals trained to lever-press for food reinforcement, carbamazepine (15 mg/kg) also significantly decreased the rate of responding, suggesting that the suppression of responding was not specific to cocaine-reinforced behavior.
来自人类的轶事证据表明,卡马西平可抑制可卡因引起的快感和渴望。但在使用安慰剂对照的对照试验中,此类说法并无依据。在本研究中,训练大鼠在每天2小时的时段内静脉注射可卡因自我给药,每按十次杠杆给予1 mg/kg可卡因。反应稳定后,在每次给药前先注射赋形剂2天,随后注射卡马西平2天。剂量为7 mg/kg时,卡马西平无作用,而15 mg/kg仅在卡马西平治疗的第二天(第4天)抑制对可卡因的反应。连续治疗4天后,卡马西平(15 mg/kg)略微但显著地降低了可卡因维持的反应。在另一组训练通过按压杠杆获取食物强化的动物中,卡马西平(15 mg/kg)也显著降低了反应速率,这表明反应的抑制并非可卡因强化行为所特有。