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氟西汀(一种用于减肥的血清素能药物)的临床前药理学

Preclinical pharmacology of fluoxetine, a serotonergic drug for weight loss.

作者信息

Yen T T, Fuller R W

机构信息

Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285.

出版信息

Am J Clin Nutr. 1992 Jan;55(1 Suppl):177S-180S. doi: 10.1093/ajcn/55.1.177s.

Abstract

Fluoxetine selectively inhibits serotonin uptake in vitro and in vivo and thus enhances serotonergic function, leading to a decrease in food intake beginning with the first dose and a decrease in body weight or in weight gain after multiple doses of fluoxetine. Fluoxetine and other drugs that increase serotonergic function decrease food intake with characteristics that make them attractive for use in weight reduction. In rats, for instance, fluoxetine and other serotonergic drugs suppress stress-induced eating, suppress carbohydrate consumption selectively, and suppress insulin-induced hyperphagia. Fluoxetine and other serotonergic drugs do not cause amphetamine-like behavioral stimulation in animals and have no known abuse or addiction liability. In obese yellow mice and in normal mice, as in rats, fluoxetine causes a sustained decrease in food intake and body weight. The pharmacologic effects of fluoxetine in animals suggest its potential use in weight-reduction programs in obese humans.

摘要

氟西汀在体内外均可选择性抑制5-羟色胺摄取,从而增强5-羟色胺能功能,从首剂用药开始即导致食物摄入量减少,多次服用氟西汀后体重下降或体重增加减少。氟西汀和其他增强5-羟色胺能功能的药物可减少食物摄入量,其特性使其在减肥中具有应用价值。例如,在大鼠中,氟西汀和其他5-羟色胺能药物可抑制应激诱导的进食,选择性抑制碳水化合物消耗,并抑制胰岛素诱导的摄食过量。氟西汀和其他5-羟色胺能药物不会在动物中引起类似苯丙胺的行为兴奋,且无已知的滥用或成瘾倾向。与在大鼠中一样,在肥胖黄色小鼠和正常小鼠中,氟西汀可导致食物摄入量和体重持续下降。氟西汀在动物中的药理作用表明其在肥胖人类减肥计划中的潜在用途。

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