Preston K L, Bigelow G E
Behavioral Pharmacology Research Unit, Department of Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J Pharmacol Exp Ther. 2000 Oct;295(1):114-24.
The purpose of this study was to examine the discrimination of agonist-antagonist opioids in humans trained in a two-choice hydromorphone/not hydromorphone discrimination. Eight adult male volunteers with histories of opioid abuse who were not currently physically dependent were trained to discriminate the mu receptor agonist hydromorphone (3 mg/70 kg, i.m.) ("Drug A") from a "Not Drug A" training condition (saline placebo). Volunteers received financial reinforcement for correct responses. After training, generalization dose-effect curves for hydromorphone, butorphanol, pentazocine, nalbuphine, and buprenorphine were determined. Other subjective, behavioral, and physiological measures were concurrently collected in all sessions. In generalization testing hydromorphone and buprenorphine produced dose-related increases in hydromorphone-appropriate responses. Pentazocine produced an inverted U-shaped dose-response curve with complete substitution at 32 mg/70 kg but not at 64 mg/70 kg. Butorphanol and nalbuphine did not completely substitute for hydromorphone at any dose tested. These results differ from an earlier two-choice, Drug A versus Drug B (hydromorphone/saline) discrimination study. After Drug/Not Drug instructions the behavioral discriminations of agonist-antagonist opioids were more consistent with their putative agonist activities at the mu opioid receptor and with their subjective effects profiles than was the case after Drug A versus Drug B instructions. These results suggest that instructions are an important factor in the outcome of human drug discrimination studies.
本研究的目的是检测在二选一氢吗啡酮/非氢吗啡酮辨别训练中人类对激动剂-拮抗剂阿片类药物的辨别能力。八名有阿片类药物滥用史且目前无身体依赖的成年男性志愿者接受训练,以区分μ受体激动剂氢吗啡酮(3毫克/70千克,肌肉注射)(“药物A”)与“非药物A”训练条件(生理盐水安慰剂)。志愿者做出正确反应可获得金钱奖励。训练后,测定了氢吗啡酮、布托啡诺、喷他佐辛、纳布啡和丁丙诺啡的泛化剂量-效应曲线。在所有实验环节中同时收集了其他主观、行为和生理指标。在泛化测试中,氢吗啡酮和丁丙诺啡产生了与剂量相关的、对氢吗啡酮适宜反应的增加。喷他佐辛产生了倒U形剂量-反应曲线,在32毫克/70千克时完全替代,但在64毫克/70千克时未完全替代。在任何测试剂量下,布托啡诺和纳布啡都不能完全替代氢吗啡酮。这些结果与早期的二选一、药物A对药物B(氢吗啡酮/生理盐水)辨别研究不同。在药物/非药物指示后,激动剂-拮抗剂阿片类药物的行为辨别与其在μ阿片受体上的假定激动剂活性及其主观效应特征比在药物A对药物B指示后更为一致。这些结果表明,指示是人类药物辨别研究结果中的一个重要因素。