Schechter M D, Finkelstein J A
Pharmacol Biochem Behav. 1985 Jul;23(1):7-11. doi: 10.1016/0091-3057(85)90121-2.
Dopamine agonists and fenfluramine were used as pharmacological probes to investigate the possible difference in sensitivity and time course of drug action in genetically obese Zucker rats and their lean littermates. All rats were trained to discriminate between the stimulus properties of 0.6 mg/kg d-amphetamine and its vehicle in a two-lever, food-motivated operant task. Once trained, both groups of rats showed a dose-related decrease in discriminative performance with lower amphetamine doses. Analysis of the dose-response curves indicated an ED50 for the obese rats of 0.17 mg/kg and for the lean group of 0.14 mg/kg. Administration of 0.3-1.2 mg/kg l-amphetamine and 2.5-10.0 mg/kg cocaine produced a pattern of responding similar to that observed with d-amphetamine. In contrast, 0.08-mg/kg apomorphine produced saline-appropriate responding and 1.5-2.5 mg/kg fenfluramine produced intermediate results in both groups. Time-course experiments indicated that the lean rats maintain errorless discriminative performance through 90 min post-injection, whereas the obese rats discriminate d-amphetamine significantly less at that post-administration time. The results suggest a similar sensitivity to d-amphetamine and other dopaminergic agonists in obese and lean rats with a difference in the time-course of d-amphetamine's action between these two groups.
多巴胺激动剂和芬氟拉明被用作药理学探针,以研究遗传性肥胖的 Zucker 大鼠及其瘦的同窝仔鼠在药物作用敏感性和时间过程方面可能存在的差异。所有大鼠都经过训练,在一个双杠杆、以食物为动机的操作性任务中区分 0.6 mg/kg d-苯丙胺及其溶媒的刺激特性。一旦训练完成,两组大鼠在较低剂量苯丙胺时的辨别性能都呈现出剂量相关的下降。剂量-反应曲线分析表明,肥胖大鼠的半数有效剂量(ED50)为 0.17 mg/kg,瘦鼠组为 0.14 mg/kg。给予 0.3 - 1.2 mg/kg l-苯丙胺和 2.5 - 10.0 mg/kg 可卡因产生的反应模式与 d-苯丙胺观察到的相似。相比之下,0.08 mg/kg 阿扑吗啡产生与生理盐水相符的反应,1.5 - 2.5 mg/kg 芬氟拉明在两组中都产生中间结果。时间过程实验表明,瘦鼠在注射后 90 分钟内保持无误的辨别性能,而肥胖大鼠在给药后该时间对 d-苯丙胺的辨别明显减少。结果表明,肥胖和瘦大鼠对 d-苯丙胺和其他多巴胺能激动剂的敏感性相似,但两组之间 d-苯丙胺作用的时间过程存在差异。