Grinker J A, Drewnowski A, Enns M, Kissileff H
Pharmacol Biochem Behav. 1980 Feb;12(2):265-75. doi: 10.1016/0091-3057(80)90367-6.
The effects of two doses of d-amphetamine and fenfluramine on male Zucker rats maintained ad lib on solid and liquid diets were investigated using the technique of meal pattern analysis. Amphetamine-induced anorexia was of short duration in both obese and lean rats. In the lean rats, anorexia was followed by rebound feeding resulting in little or no reduction in total daily intake. The drug reduced meal sizes of obese but not lean rats and caused a transient decrease in meal frequency. Increased spontaneous activity paralleled the decreased food intake. In contrast, anorexia following fenfluramine was greater, more prolonged and of equivalent magnitude in obese and in lean rats. No rebound feeding was observed. Reduction in intake was achieved primarily by changes in meal size rather than in meal frequency. These data demonstrate that food intakes of genetically obese Zucker rats are more susceptible to the action of d-amphetamine than those of lean rats, and are consistent with reports of differential neurotransmitter levels in the obese and lean rats.
采用进餐模式分析技术,研究了两剂量的右旋苯丙胺和芬氟拉明对随意进食固体和液体食物的雄性 Zucker 大鼠的影响。苯丙胺引起的厌食在肥胖和瘦大鼠中持续时间都很短。在瘦大鼠中,厌食之后是反弹性进食,导致每日总摄入量几乎没有减少或没有减少。该药物减小了肥胖大鼠的餐量,但对瘦大鼠没有影响,并导致进餐频率短暂下降。自发活动增加与食物摄入量减少平行。相比之下,芬氟拉明引起的厌食在肥胖和瘦大鼠中更严重、持续时间更长且程度相当。未观察到反弹性进食。摄入量的减少主要是通过餐量的变化而不是进餐频率的变化实现的。这些数据表明,遗传性肥胖 Zucker 大鼠的食物摄入量比瘦大鼠更容易受到右旋苯丙胺作用的影响,并且与肥胖和瘦大鼠中神经递质水平差异的报道一致。