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甲状腺胺抑制质膜和囊泡单胺转运。

Thyronamines inhibit plasma membrane and vesicular monoamine transport.

作者信息

Snead Aaron N, Santos Magda S, Seal Rebecca P, Miyakawa Motonori, Edwards Robert H, Scanlan Thomas S

机构信息

Graduate Program in Chemistry and Chemical Biology, University of California at San Francisco, San Francisco, California 94143, USA.

出版信息

ACS Chem Biol. 2007 Jun 15;2(6):390-8. doi: 10.1021/cb700057b. Epub 2007 May 25.

Abstract

Thyroid hormone has long been known to have important transcriptional regulatory activities. Recently, however, the presence of endogenous derivatives of thyroid hormone, thyronamines, has been reported in various mammalian tissues. These derivatives have potent in vitro activity with a class of orphan G-protein-coupled receptors, the trace amine-associated receptors, and profound in vivo effects when administered to mice. We report here a novel neuromodulatory role for thyronamines. In synaptosomal preparations and heterologous expression systems, thyronamines act as specific dopamine and norepinephrine reuptake inhibitors. Thyronamines also inhibit the transport of monoamines into synaptic vesicles. These observations expand the nontranscriptional role of thyroid hormone derivatives and may help to explain the pharmacological effects of thyronamines in vivo.

摘要

长期以来,人们都知道甲状腺激素具有重要的转录调节活性。然而,最近有报道称,在各种哺乳动物组织中存在甲状腺激素的内源性衍生物——甲状腺胺。这些衍生物对一类孤儿G蛋白偶联受体(痕量胺相关受体)具有强大的体外活性,并且在给小鼠注射时会产生深远的体内效应。我们在此报告甲状腺胺的一种新的神经调节作用。在突触体制剂和异源表达系统中,甲状腺胺可作为特定的多巴胺和去甲肾上腺素再摄取抑制剂。甲状腺胺还能抑制单胺转运到突触小泡中。这些观察结果扩展了甲状腺激素衍生物的非转录作用,可能有助于解释甲状腺胺在体内的药理作用。

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