Colpaert F C, Niemegeers C J, Janssen P A
Arch Int Pharmacodyn Ther. 1977 Feb;225(2):308-16.
Using a two-lever food-reinforced operant procedure, rats (n=11) were trained to discriminate the narcotic analgesic fentanyl (0.04 mg/kg, s.c.) from saline. In rats so trained, alpha methyl-p-tyrosine (150 mg/kg, i.p.) was found not to affect the discriminability of fentanyl. Pretreatment (s.c.) with either adrenolytic compounds (10 mg/kg aceperone, 40 mg/kg dibenamine, 10 mg/kg phenoxybenzamine, 20 mg/kg propranolol) or sedative neuroleptics (0.63 mg/kg azaperone, 1.25 mg/kg chlorpromazine, 10 mg/kg pipamperone) likewise failed to attenuate the narcotic cue. Pimozide (0.63 mg/kg) and, to some extent, spiperone (0.04 mg/kg) reduced the percentage of responding on the selected lever, and pimozide antagonized drug lever selection in some animals. The results suggest that specific neuroleptics (e.g. pimozide) may affect the subjective effects induced by narcotics in humans.
采用双杠杆食物强化操作性程序,对11只大鼠进行训练,使其能够区分麻醉性镇痛药芬太尼(0.04毫克/千克,皮下注射)和生理盐水。在经过如此训练的大鼠中,发现α-甲基对酪氨酸(150毫克/千克,腹腔注射)并不影响芬太尼的辨别能力。用抗肾上腺素化合物(10毫克/千克醋哌隆、40毫克/千克双苄胺、10毫克/千克酚苄明、20毫克/千克普萘洛尔)或镇静性抗精神病药(0.63毫克/千克阿扎哌隆、1.25毫克/千克氯丙嗪、10毫克/千克匹泮哌隆)进行预处理(皮下注射)同样未能减弱麻醉提示。匹莫齐特(0.63毫克/千克)以及在一定程度上螺哌隆(0.04毫克/千克)降低了在选定杠杆上的反应百分比,并且匹莫齐特在一些动物中拮抗了药物杠杆选择。结果表明,特定的抗精神病药(如匹莫齐特)可能会影响人类中麻醉药引起的主观效应。