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大鼠脑功能性5-羟色胺转运体的克隆与表达

Cloning and expression of a functional serotonin transporter from rat brain.

作者信息

Blakely R D, Berson H E, Fremeau R T, Caron M G, Peek M M, Prince H K, Bradley C C

机构信息

Department of Anatomy and Cell Biology, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

Nature. 1991 Nov 7;354(6348):66-70. doi: 10.1038/354066a0.

Abstract

Selective antagonism of serotonin (5-hydroxytryptamine, 5HT) and noradrenaline transport by antidepressants is a key element in the 'amine' hypothesis of affective disorders. Uptake and/or transport sites of 5HT have been reported to be reduced in platelets of patients suffering from depression and in post-mortem brain samples of depressed patients and suicide victims. To date there has been little molecular information available on the structure and regulation of 5HT transporters. Using the polymerase chain reaction with degenerate oligonucleotides derived from two highly conserved regions of the transporters for noradrenaline and gamma-aminobutyric acid (GABA), we have identified a large family of related gene products expressed in rodent brain. One of these products hybridizes to a single 3.7-kilobase RNA restricted to rat midbrain and brainstem, where it is highly enriched within the serotonergic raphe complex. Transfection with a single 2.3-kilobase brainstem complementary DNA clone is sufficient to confer expression of a Na(+)-dependent 5HT transporter upon nonneural cells, with transport selectively and potently antagonized by 5HT uptake-specific antidepressants, including paroxetine, citalopram and fluoxetine.

摘要

抗抑郁药对血清素(5-羟色胺,5HT)和去甲肾上腺素转运的选择性拮抗作用是情感障碍“胺”假说的关键要素。据报道,抑郁症患者的血小板以及抑郁症患者和自杀受害者的死后脑样本中5HT的摄取和/或转运位点减少。迄今为止,关于5HT转运体的结构和调节的分子信息很少。利用聚合酶链反应,使用源自去甲肾上腺素和γ-氨基丁酸(GABA)转运体两个高度保守区域的简并寡核苷酸,我们在啮齿动物脑中鉴定出了一大类相关基因产物。其中一种产物与一种单一的3.7千碱基RNA杂交,该RNA局限于大鼠中脑和脑干,在血清素能中缝复合体内高度富集。用一个2.3千碱基的脑干互补DNA克隆进行转染足以使非神经细胞表达一种依赖Na(+)的5HT转运体,其转运被5HT摄取特异性抗抑郁药选择性且有效地拮抗,这些抗抑郁药包括帕罗西汀、西酞普兰和氟西汀。

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