Moses P L, Wurtman R J
Life Sci. 1984 Sep 17;35(12):1297-300. doi: 10.1016/0024-3205(84)90101-2.
The effects of five anorexic agents on food consumption were tested in rats offered single, isocaloric, isonitrogenous diets differing in carbohydrate content. Three of the test agents, d-amphetamine, benzphetamine and chlorphentermine, are sympathomimetic and cause CNS stimulation; the others, MK-212 and d-fenfluramine, are thought to facilitate serotonin-mediated neurotransmission. At ED50 doses, the sympathomimetic drugs reduced food consumption whether the test diet was rich (75% dextrin) or poor (25% dextrin) in carbohydrate. In contrast, MK-212 and d-fenfluramine failed to reduce consumption of the 25% dextrin test diet. These observations suggest that anorexic drugs like d-amphetamine and d-fenfluramine do not act via a common "amphetamine receptor," and are compatible with earlier observations, made on rats given diet pairs simultaneously, that enhanced serotoninergic neurotransmission selectively suppresses appetite for carbohydrates.
在给大鼠提供碳水化合物含量不同但热量和氮含量相同的单一饮食的情况下,测试了五种厌食剂对食物消耗的影响。三种受试药物,即右旋苯丙胺、苄非他明和氯苯丁胺,是拟交感神经药,会引起中枢神经系统刺激;另外两种,MK - 212和右旋芬氟拉明,被认为可促进5-羟色胺介导的神经传递。在半数有效剂量(ED50)下,无论受试饮食的碳水化合物含量高(75%糊精)还是低(25%糊精),拟交感神经药物都会减少食物消耗。相比之下,MK - 212和右旋芬氟拉明未能减少25%糊精受试饮食的消耗量。这些观察结果表明,像右旋苯丙胺和右旋芬氟拉明这样的厌食药物并非通过共同的“苯丙胺受体”起作用,这与早期对同时给予成对饮食的大鼠所做的观察结果相符,即增强的5-羟色胺能神经传递会选择性地抑制对碳水化合物的食欲。