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新型食欲抑制剂(--)-苏式-氯柠檬酸作用机制的研究

Studies on the mechanism of action of a novel anorectic agent, (--)-threo-chlorocitric acid.

作者信息

Triscari J, Sullivan A C

出版信息

Pharmacol Biochem Behav. 1981 Aug;15(2):311-8. doi: 10.1016/0091-3057(81)90193-3.

Abstract

(--)-threo-Chlorocitric acid, a novel and potent anorectic agent in rats and dogs, decreased food intake to a comparable extent in rats fed chow, low fat, or high fat diets. This inhibition of food intake was not the result of conditioned aversion. Unlike (--)-threo-hydroxycitric acid, a structurally related compound which inhibits fatty acid synthesis, (--)-threo-chlorocitric acid did not suppress fatty acid synthesis in an isolated hepatocyte system or in vivo. (--)-threo-Chlorocitric acid significantly delayed the rate of gastric emptying. Of the four stereoisomers of chlorocitric acid, (--)-threo-chlorocitric acid was the most active both in delaying gastric emptying and producing anorexia in rats. It is suggested that the mechanism by which (--)-threo-chlorocitric acid may suppress food intake is through a reduction of gastric emptying.

摘要

(-)-苏式-氯柠檬酸是一种在大鼠和犬类中新型且强效的食欲抑制剂,在喂食普通饲料、低脂或高脂饮食的大鼠中,它能使食物摄入量减少到相当程度。这种对食物摄入的抑制并非条件性厌恶的结果。与结构相关的化合物(-)-苏式-羟基柠檬酸不同,后者抑制脂肪酸合成,而(-)-苏式-氯柠檬酸在分离的肝细胞系统或体内均不抑制脂肪酸合成。(-)-苏式-氯柠檬酸显著延迟胃排空速率。在氯柠檬酸的四种立体异构体中,(-)-苏式-氯柠檬酸在延迟大鼠胃排空和产生厌食方面最为活跃。有人提出,(-)-苏式-氯柠檬酸抑制食物摄入的机制可能是通过减少胃排空。

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