Stewart J, Wise R A
Department of Psychology, Concordia University, Montreal, Quebec, Canada.
Psychopharmacology (Berl). 1992;108(1-2):79-84. doi: 10.1007/BF02245289.
The effects of morphine, naltrexone, and nalorphine were studied in rats trained to lever-press for intravenous heroin and then tested under conditions of non-reinforcement. Animals were reinforced for lever-pressing on a continuous reinforcement schedule (100 micrograms/kg per infusion) for 2-3 h each day following which reinforcement was terminated and animals were studied under extinction conditions for the remainder of the session. Each day following the termination of responding under extinction conditions, animals were given a single injection of saline, morphine, nalorphine, or naltrexone; lever-pressing under the extinction conditions was then observed for several hours. When animals adapted to this regimen, very low levels of responding were seen following saline injections; morphine (2 or 10 mg/kg) reinstated vigorous responding that lasted 1-4 h. Naltrexone (2 mg/kg) suppressed responding below the levels seen after saline, and nalorphine (10 mg/kg) had the same effect as saline. These observations support the view that opioid-seeking behavior is primed by the proponent or opioid-like actions of opioids and not by the opponent or drug-opposite effects associated with opioid withdrawal.
在训练大鼠通过按压杠杆静脉注射海洛因,然后在无强化条件下进行测试的实验中,研究了吗啡、纳曲酮和烯丙吗啡的作用。动物每天按照连续强化程序(每次输注100微克/千克)按压杠杆进行强化,持续2 - 3小时,之后停止强化,在剩余实验时段让动物在消退条件下接受研究。在消退条件下停止反应后的每一天,给动物单次注射生理盐水、吗啡、烯丙吗啡或纳曲酮;然后观察动物在消退条件下按压杠杆的情况数小时。当动物适应此方案后,注射生理盐水后反应水平非常低;吗啡(2或10毫克/千克)恢复了持续1 - 4小时的强烈反应。纳曲酮(2毫克/千克)使反应低于注射生理盐水后的水平,而烯丙吗啡(10毫克/千克)的作用与生理盐水相同。这些观察结果支持这样一种观点,即寻求阿片类药物的行为是由阿片类药物的支持性或类阿片样作用引发的,而非由与阿片类药物戒断相关的对抗性或药物相反作用引发。