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厌食剂量的氟西汀不具备多巴胺摄取抑制剂的特性。

Fluoxetine at anorectic doses does not have properties of a dopamine uptake inhibitor.

作者信息

Fuller R W, Hemrick-Luecke S K, Snoddy H D

机构信息

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN.

出版信息

J Neural Transm Gen Sect. 1994;96(3):165-77. doi: 10.1007/BF01294784.

Abstract

Although fluoxetine is a highly selective inhibitor of serotonin uptake in vitro and in vivo, some investigators have suggested that dopamine uptake inhibition may contribute to anorectic actions of fluoxetine. The present experiments were done to determine fluoxetine's effects in some animal protocols in which dopamine uptake inhibitors have characteristic actions. Mazindol prevented the depletion of striatal dopamine and its metabolites by amphetamine in iprindole-pretreated rats, but fluoxetine had no effect. Mazindol prevented the depletion of striatal dopamine and its metabolites by 6-hydroxydopamine injected intracerebroventricularly into rats, but fluoxetine had no effect. Mazindol enhanced the elevation of 3,4-dihydroxyphenylacetic acid concentration in rat brain after spiperone injection, but fluoxetine did not cause that effect. Fluoxetine did not mimic amfonelic acid in antagonizing the retention of alpha-methyl-m-tyramine invant striatum after the injection of alpha-methyl-m-tyrosine. These results show that fluoxetine, at doses that are effective in blocking the serotonin uptake carrier and causing anorexia, does not block the dopamine uptake carrier.

摘要

尽管氟西汀在体外和体内都是一种高度选择性的血清素摄取抑制剂,但一些研究人员认为,多巴胺摄取抑制可能有助于氟西汀的厌食作用。进行本实验是为了确定氟西汀在一些动物实验中的作用,在这些实验中多巴胺摄取抑制剂具有特征性作用。吗茚酮可防止苯丙胺在异吲哚预处理大鼠中耗竭纹状体多巴胺及其代谢产物,但氟西汀没有效果。吗茚酮可防止脑室内注射6-羟基多巴胺对大鼠纹状体多巴胺及其代谢产物的耗竭,但氟西汀没有效果。吗茚酮可增强大鼠脑内注射舒必利后3,4-二羟基苯乙酸浓度的升高,但氟西汀没有此作用。在注射α-甲基-m-酪氨酸后,氟西汀在拮抗α-甲基-m-酪胺在完整纹状体中的潴留方面,并不模拟安非他明酸的作用。这些结果表明,在有效阻断血清素摄取载体并导致厌食的剂量下,氟西汀不会阻断多巴胺摄取载体。

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