Pabello N G, Hubbell C L, Cavallaro C A, Barringer T M, Mendez J J, Reid L D
Laboratory for Psychopharmacology, Rensselaer Polytechnic Institute, Troy, NY 12180-3590, USA.
Pharmacol Biochem Behav. 1998 Oct;61(2):181-92. doi: 10.1016/s0091-3057(98)00084-7.
Rats, fixed with chronically indwelling electrodes for electrical intracranial stimulation (ICS) of the lateral hypothalamus, were taught to press a bar for ICS. Once pressing rates became stable, during daily 20-min sessions, rats were given cocaine (5 or 20 mg/kg) before the sessions. When given daily, cocaine consistently enhanced rates of pressing. When a combination of small doses of isradipine (e.g., 1 mg/kg) and naltrexone (3 mg/kg) were given before cocaine administration. the combination blocked cocaine's enhancement of pressing for ICS. The combination, however, neither reduced rates of pressing below those observed under placebos (i.e., baseline conditions) nor reduced rates when no cocaine was given. Naltrexone and isradipine (in the dose used in the combination) by themselves did not block cocaine's effects. This profile of effects indicates that a combination of isradipine and naltrexone is apt to be useful in treating cocaine use disorders.
通过长期植入电极对大鼠下丘脑外侧进行电刺激(ICS),训练大鼠按压杠杆以获得电刺激。一旦按压频率稳定,在每天20分钟的实验时段内,于实验前给大鼠注射可卡因(5或20毫克/千克)。每日给药时,可卡因持续提高按压频率。在给予可卡因之前,先给予小剂量的伊拉地平(例如1毫克/千克)和纳曲酮(3毫克/千克)的组合,该组合可阻断可卡因对按压杠杆以获得电刺激频率的提高作用。然而,该组合既未使按压频率降至低于安慰剂组(即基线条件)所观察到的频率,在未给予可卡因时也未降低按压频率。纳曲酮和伊拉地平(组合中使用的剂量)单独使用时并未阻断可卡因的作用。这种效应表明伊拉地平与纳曲酮的组合可能对治疗可卡因使用障碍有用。