van Ree J M, Slangen J L, de Wied D
J Pharmacol Exp Ther. 1978 Mar;204(3):547-57.
A standardized self-administration procedure in rats was used to determine the intravenous self-administration liability of graded doses of various drugs. Self-administration was reliably established with the tested addictive drugs (morphine, heroin, fentanyl and d-amphetamine), but not with the nonaddictive drugs (chlorpromazine and nalorphine). However, 1 out of 14 animals on nalorphine clearly demonstrated self-administering behavior. Self-administration was observed with delta1-tetrahydrocannabinol, but the percentage of animals (40% on the highest dose) that initiated this behavior and the amount of drug intake were low in comparison with amphetamine and narcotics. Concerning the narcotic drugs, approximate ED50 values for self-administration under the described conditions were calculated (morphine: 0.65; heroin: 0.05; fentanyl: 0.0025 mg/kg/injection). Total daily drug intake was related to the unit dose delivered per injection in that a higher drug dosage led to more drug intake. In experiments with heroin, this relationship was not caused by prior forced injections. The approximate ED50 value for amphetamine appeared to be 0.145 mg/kg/injection. Narcotic drug administration resulted in a disturbance of the patterns of food and water intake. Shortly after drug administration food intake was stimulated, followed by an increased consumption of water. The patterns of food and water intake remained disturbed in animals showing self-injecting behavior. With amphetamine both the quantity of food and the frequency of eating were reduced. These effects were observed only temporarily in animals tested without prior forced injections. The present results indicate that measuring the reinforcing efficacy of drugs under strictly defined experimental conditions provides quantitative criteria for intravenous self-administration of drugs in rats.
采用标准化的大鼠自我给药程序,以确定不同药物分级剂量的静脉自我给药倾向。受试的成瘾性药物(吗啡、海洛因、芬太尼和右旋苯丙胺)可可靠地建立自我给药行为,但非成瘾性药物(氯丙嗪和烯丙吗啡)则不能。然而,14只接受烯丙吗啡的动物中有1只明显表现出自我给药行为。δ1-四氢大麻酚可观察到自我给药行为,但与苯丙胺和麻醉药品相比,开始出现这种行为的动物百分比(最高剂量时为40%)和药物摄入量较低。关于麻醉药品,计算了在所述条件下自我给药的近似半数有效剂量(ED50)值(吗啡:0.65;海洛因:0.05;芬太尼:0.0025毫克/千克/注射)。每日药物总摄入量与每次注射给予的单位剂量相关,即较高的药物剂量导致更多的药物摄入。在用海洛因进行的实验中,这种关系并非由先前的强制注射引起。苯丙胺的近似ED50值似乎为0.145毫克/千克/注射。给予麻醉药品会导致食物和水摄入模式紊乱。给药后不久,食物摄入量会增加,随后饮水量也会增加。在表现出自我注射行为的动物中,食物和水的摄入模式仍然紊乱。使用苯丙胺时,食物量和进食频率都会降低。这些效应仅在未进行过先前强制注射的受试动物中暂时观察到。目前的结果表明,在严格定义的实验条件下测量药物的强化效力,可为大鼠静脉自我给药提供定量标准。