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血清素能食欲抑制药物药理学的最新进展。

An update on the pharmacology of serotoninergic appetite-suppressive drugs.

作者信息

Garattini S

机构信息

Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

Int J Obes Relat Metab Disord. 1992 Dec;16 Suppl 4:S41-8.

PMID:1338385
Abstract

D-Fenfluramine, fluoxetine and sertraline are considered to be serotoninergic appetite-suppressive drugs. These three agents have been compared in fasted mice, rats and guinea pigs for their activity as food intake inhibitors. D-Fenfluramine is the most effective drug in the three animal species followed by fluoxetine and then sertraline. All three compounds are metabolized to N-dealkylated metabolites which accumulate in the brain and are themselves effective in reducing food intake. At anorectic doses the brain levels of the drugs and their metabolites are compatible with the concentrations able to block serotonin (5-HT) uptake and to release brain 5-HT from brain synaptosomes. However only the anorectic activity of D-fenfluramine is antagonized by the previous administration of 5-HT antagonists. These results cast some doubts on the role of brain 5-HT in explaining the anorectic activity of fluoxetine and sertraline.

摘要

右旋芬氟拉明、氟西汀和舍曲林被认为是具有血清素能的食欲抑制药物。在禁食的小鼠、大鼠和豚鼠中对这三种药物作为食物摄入抑制剂的活性进行了比较。右旋芬氟拉明在这三种动物物种中是最有效的药物,其次是氟西汀,然后是舍曲林。所有这三种化合物都代谢为N-去烷基化代谢物,这些代谢物在大脑中积累,并且自身在减少食物摄入方面有效。在产生厌食作用的剂量下,药物及其代谢物的脑内水平与能够阻断血清素(5-羟色胺)摄取并从脑突触体释放脑5-羟色胺的浓度相符。然而,只有右旋芬氟拉明的厌食活性会被预先给予的5-羟色胺拮抗剂所拮抗。这些结果对脑5-羟色胺在解释氟西汀和舍曲林的厌食活性方面的作用提出了一些疑问。

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