Spyraki C, Fibiger H C, Phillips A G
Brain Res. 1982 Dec 16;253(1-2):195-203. doi: 10.1016/0006-8993(82)90686-2.
The conditioned place preference paradigm was used to investigate the reinforcing properties of cocaine. Rats were injected (i.p.) with cocaine hydrochloride (0.625-20 mg/kg) and then immediately confined for 30 min to one side of a shuttle box in which each of the two compartments had distinctive features. On alternate (control) days they received saline injections and were confined for 30 min to the opposite side. Cocaine produced a significant, dose-related preference for the distinctive environment that previously had been paired with the drug. Pretreatment with pimozide (0.5 or 1.0 mg/kg) or haloperidol (1.0 mg/kg), both of which blocked the locomotor stimulant effects of cocaine, failed to influence place preference produced by cocaine (5.0 mg/kg). In addition, neither 6-hydroxydopamine lesions of dopamine terminals in the nucleus accumbens nor 6-hydroxydopamine-induced destruction of central and/or peripheral noradrenergic systems affected cocaine-induced place preference conditioning. In other experiments it was found that injections of the local anaesthetic procaine, at doses that did not affect locomotor activity (25 and 50 mg/kg), also resulted in significant place preference conditioning. It is concluded that cocaine can produce place preference conditioning through a mechanism that is independent of its effects on catecholamine-containing neurons and that may be related to its local anaesthetic properties. It is noted, however, that if cocaine's local anaesthetic properties could be blocked selectively, the drug might still produce place preference conditioning through its enhancement of central dopaminergic function.
采用条件性位置偏爱范式研究可卡因的强化特性。给大鼠腹腔注射盐酸可卡因(0.625 - 20毫克/千克),然后立即将其限制在穿梭箱的一侧30分钟,该穿梭箱的两个隔室各有独特特征。在交替的(对照)日子里,给它们注射生理盐水,并将其限制在另一侧30分钟。可卡因产生了对先前与药物配对的独特环境的显著的、剂量相关的偏爱。用匹莫齐特(0.5或1.0毫克/千克)或氟哌啶醇(1.0毫克/千克)预处理,这两种药物均能阻断可卡因的运动兴奋作用,但未能影响可卡因(5.0毫克/千克)产生的位置偏爱。此外,伏隔核中多巴胺末梢的6 - 羟基多巴胺损伤以及6 - 羟基多巴胺诱导的中枢和/或外周去甲肾上腺素能系统的破坏均未影响可卡因诱导的位置偏爱条件反射。在其他实验中发现,注射局部麻醉药普鲁卡因,剂量不影响运动活性(25和50毫克/千克),也导致显著的位置偏爱条件反射。得出的结论是,可卡因可通过一种独立于其对含儿茶酚胺神经元作用的机制产生位置偏爱条件反射,且该机制可能与其局部麻醉特性有关。然而,需要注意的是,如果可卡因的局部麻醉特性能够被选择性阻断,该药物仍可能通过增强中枢多巴胺能功能产生位置偏爱条件反射。