Thyronamines inhibit plasma membrane and vesicular monoamine transport

被引:46
作者
Snead, Aaron N.
Santos, Magda S.
Seal, Rebecca P.
Miyakawa, Motonori
Edwards, Robert H.
Scanlan, Thomas S.
机构
[1] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97239 USA
[2] Univ Calif San Francisco, Grad Program Chem & Chem Biol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Neurol & Physiol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Pharmaceut Chem & Cellular, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Mol Pharmacol, San Francisco, CA 94143 USA
关键词
D O I
10.1021/cb700057b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:390 / 398
页数:9
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