Brindley D N, Saxton J, Shahidullah H, Armstrong M
Biochem Pharmacol. 1985 Apr 15;34(8):1265-71. doi: 10.1016/0006-2952(85)90504-0.
Rats were maintained on a corn oil diet and treated with D-fenfluramine at doses of 2.5 mg/kg twice a day for 11 days or with 10 mg or 25 mg/kg once a day for 12 days. The lower dose of D-fenfluramine produced no marked changes in body weight and after 11 days of treatment the weights of the rats on average were only 2% lower than the controls. The food intake of these rats was only decreased on the first day. The two higher doses of D-fenfluramine decreased the food consumption for about 3 days but thereafter it was similar to that of the control rats. The body weight of these rats fell on the first day, but after about four days the gain in body weight paralleled rather than approached that of the control rats. Increasing the dose of D-fenfluramine progressively decreased the relative size of the epididymal fat pad. At the end of the treatment period the rats were fed acutely with fructose to increase the circulating concentrations of corticosterone and to stimulate triacylglycerol synthesis. All three doses of D-fenfluramine decreased the concentration of circulating triacylglycerol after fructose feeding. The 10 mg/kg dose also decreased the basal concentration of triacylglycerol. The two higher doses of fenfluramine decreased the rises in the circulating concentrations of corticosterone, glycerol and fatty acids that are produced by fructose feeding. The basal concentrations of these compounds in the absence of fructose feeding were not significantly affected by the 10 mg/kg dose of D-fenfluramine. The possible relationship between the effect of chronic treatment with D-fenfluramine in decreasing a metabolic stress response and lipolysis is discussed relative to its hypotriglyceridaemic action and its effect on body weight-set point. The results demonstrate that D-fenfluramine produced persistent changes in metabolism at a time when the treated rats were growing at the same rate as the control rats and when they were eating similar quantities of food.
大鼠以玉米油为食,每天两次给予2.5毫克/千克剂量的右旋芬氟拉明,持续11天;或以每天一次给予10毫克/千克或25毫克/千克剂量,持续12天。较低剂量的右旋芬氟拉明对体重没有显著影响,治疗11天后,大鼠的平均体重仅比对照组低2%。这些大鼠的食物摄入量仅在第一天有所减少。两种较高剂量的右旋芬氟拉明使食物消耗量减少了约3天,但此后与对照大鼠相似。这些大鼠的体重在第一天下降,但大约四天后,体重增加与对照大鼠相当而非接近。增加右旋芬氟拉明的剂量会逐渐减小附睾脂肪垫的相对大小。在治疗期结束时,给大鼠急性喂食果糖以提高皮质酮的循环浓度并刺激三酰甘油合成。所有三种剂量的右旋芬氟拉明在喂食果糖后均降低了循环三酰甘油的浓度。10毫克/千克剂量也降低了三酰甘油的基础浓度。两种较高剂量的芬氟拉明降低了果糖喂食引起的皮质酮、甘油和脂肪酸循环浓度的升高。在不喂食果糖的情况下,这些化合物的基础浓度不受10毫克/千克剂量的右旋芬氟拉明的显著影响。相对于其降甘油三酯作用及其对体重设定点的影响,讨论了长期用右旋芬氟拉明治疗在降低代谢应激反应和脂肪分解方面的可能关系。结果表明,在治疗大鼠与对照大鼠以相同速度生长且进食量相似时,右旋芬氟拉明在代谢方面产生了持续变化。