Woolverton William L, Wang Zhixia
Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Guyton Research Building, 2500 North State Street, Jackson, MS 39216-4505, USA.
Eur J Pharmacol. 2004 Feb 23;486(3):251-7. doi: 10.1016/j.ejphar.2004.01.003.
Among drugs that can function as positive reinforcers, slower occupancy of central nervous system sites of action has been associated with diminished reinforcing strength. The present study examined the relative reinforcing strength of cocaine, and the rate of in vivo dopamine transporter binding, as a function of injection duration. Rhesus monkeys (N=5) were allowed to self-administer cocaine under a progressive-ratio schedule with doses injected over different times (10-600 s). An ex vivo dopamine transporter binding assay was used to examine kinetics of in vivo transporter occupancy by cocaine injected over the same times in rats. Cocaine was a weaker reinforcer, and dopamine transporter binding rate decreased, with slower injections. Maximum transporter binding was the same across injection durations. These results support the hypothesis that slower onset of action is associated with a slower transporter occupancy and diminished reinforcing strength. Relative strength as a reinforcer may not be determined by maximum occupancy, at least not exclusively.
在可作为正性强化物发挥作用的药物中,中枢神经系统作用位点的占据速度较慢与强化强度减弱有关。本研究考察了可卡因的相对强化强度以及体内多巴胺转运体结合速率与注射持续时间的关系。恒河猴(N = 5)在累进比率方案下自行注射可卡因,注射剂量在不同时间(10 - 600秒)内给予。采用离体多巴胺转运体结合试验来检测大鼠在相同时间内注射可卡因后体内转运体占据的动力学情况。注射速度较慢时,可卡因作为强化物的作用较弱,多巴胺转运体结合速率降低。不同注射持续时间下,转运体的最大结合量相同。这些结果支持了以下假设:起效较慢与转运体占据较慢以及强化强度减弱有关。作为强化物的相对强度可能并非由最大占据量决定,至少不完全由其决定。