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(-)-苏式-氯柠檬酸:一种新型食欲抑制剂。

(--)-threo-Chlorocitric acid: a novel anorectic agent.

作者信息

Sullivan A C, Dairman W, Triscari J

出版信息

Pharmacol Biochem Behav. 1981 Aug;15(2):303-10. doi: 10.1016/0091-3057(81)90192-1.

Abstract

A new class of peripherally acting anorectics is described in these studies. The four stereoisomers of chlorocitric acid which are structurally similar to the known anorectic, (--)-threo-hydroxycitric acid, all suppressed food intake when administered at high doses to rats. Only one of these isomers, (--)-threo-chlorocitric acid, retained its anorectic activity at lower doses. The anorectic potency of (--)-threo-chlorocitric acid was approximately 40-fold greater in dogs than in lean and obese rats. The decreased food intake in rats resulted in a significant reduction of body lipid, without affecting protein levels. In contrast to the tolerance which was observed with the continued administration of mazindol or diethylpropion, tolerance to the anorectic effect of (--)-threo-chlorocitric acid did not develop. These studies suggest that (--)-threo-chlorocitric acid might be useful as an antiobesity agent.

摘要

这些研究描述了一类新型的外周作用性食欲抑制剂。氯柠檬酸的四种立体异构体在结构上与已知的食欲抑制剂(--)-苏式羟基柠檬酸相似,当以高剂量给大鼠给药时,它们均能抑制食物摄入。这些异构体中只有一种,即(--)-苏式氯柠檬酸,在较低剂量下仍保留其食欲抑制活性。(--)-苏式氯柠檬酸在犬中的食欲抑制效力比在瘦大鼠和肥胖大鼠中大约高40倍。大鼠食物摄入量的减少导致体内脂质显著减少,而不影响蛋白质水平。与持续给予马吲哚或二乙胺苯丙酮所观察到的耐受性不同,对(--)-苏式氯柠檬酸的食欲抑制作用未产生耐受性。这些研究表明,(--)-苏式氯柠檬酸可能作为一种抗肥胖剂有用。

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