Ahmed S H, Koob G F
Division of Psychopharmacology, Department of Neuropharmacology, CVN-7, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Psychopharmacology (Berl). 1999 Oct;146(3):303-12. doi: 10.1007/s002130051121.
When access time to a continuous schedule of drug self-administration is restricted, animals tend to limit intake to a certain level over time and across doses. This observation suggests an endogenous constraint or set point that determines the individual's preferred level of pharmacological effects.
To assess whether the transition to increased levels of drug intake is associated with a change in set point.
Two groups of rats were trained on a 1-h continuous schedule of cocaine self-administration (250 microg/injection), after which access to cocaine was increased to 6 h in one group (Long Access or LgA rats) or kept to 1 h in the other group (Short Access or ShA rats). After 22 sessions on this regimen, different doses of cocaine were tested (31.25, 62.5, 125, and 250 microg/injection). For each dose, the post-response time-out period was reduced to 4 s to reduce any temporal limitations on self-injections and subjects were tested several times.
In LgA rats, the first hour intake escalated over time and eventually reached a level 200% greater than that of ShA rats. Though all rats maintained relatively constant intake across doses, LgA rats took nearly two times as much cocaine than ShA rats. When access to cocaine for LgA rats was reduced to 1 h, intake returned very slowly toward pre-escalation levels but was still elevated even after 2 months of reduced availability.
These data suggest that the transition to escalated levels of intake is associated with a long-lasting change in cocaine set point.
当药物自我给药的连续时间表的获取时间受到限制时,随着时间的推移和剂量的增加,动物倾向于将摄入量限制在一定水平。这一观察结果表明存在一种内源性限制或设定点,它决定了个体对药理作用的偏好水平。
评估药物摄入量增加的转变是否与设定点的变化有关。
两组大鼠接受了1小时连续可卡因自我给药训练(250微克/注射),之后一组大鼠(长获取组或LgA大鼠)的可卡因获取时间增加到6小时,另一组大鼠(短获取组或ShA大鼠)保持在1小时。在该方案进行22次实验后,测试了不同剂量的可卡因(31.25、62.5、125和250微克/注射)。对于每个剂量,将反应后的超时时间缩短至4秒,以减少对自我注射的任何时间限制,并对受试者进行了多次测试。
在LgA大鼠中,最初1小时的摄入量随时间增加,最终达到比ShA大鼠高200%的水平。尽管所有大鼠在不同剂量下的摄入量相对保持恒定,但LgA大鼠摄入的可卡因几乎是ShA大鼠的两倍。当LgA大鼠的可卡因获取时间减少到1小时时,摄入量非常缓慢地恢复到预增加水平,但即使在获取时间减少2个月后仍高于该水平。
这些数据表明,摄入量增加的转变与可卡因设定点的长期变化有关。