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去甲肾上腺素转运体及其调节。

The norepinephrine transporter and its regulation.

作者信息

Mandela Prashant, Ordway Gregory A

机构信息

Department of Pharmacology & Toxicology, University of Mississippi Medical Center, Jackson, USA.

出版信息

J Neurochem. 2006 Apr;97(2):310-33. doi: 10.1111/j.1471-4159.2006.03717.x. Epub 2006 Mar 15.

Abstract

For many years, the norepinephrine transporter (NET) was considered a 'static' protein that contributed to the termination of the action of norepinephrine in the synapse of noradrenergic neurons. The concept that the NET is dynamically regulated, adjusting noradrenergic transmission by changing its function and/or expression, was considered initially in the mid 1980s. Since that time, a plethora of studies demonstrate that the NET is regulated by several intracellular and extracellular signaling molecules, and that phosphorylation of the NET is a major pathway regulating its cell surface expression and thereby its function. The NET is a target of action of a number of drugs that are used long-term therapeutically or abused chronically. This has driven numerous investigations of how the NET and its function are regulated by long-term exposure to drugs. While repeated exposure to many drugs has been shown to affect NET function and expression, the intracellular mechanisms for these effects remains elusive.

摘要

多年来,去甲肾上腺素转运体(NET)被认为是一种“静态”蛋白,它在去甲肾上腺素能神经元的突触中参与去甲肾上腺素作用的终止。NET受到动态调节,通过改变其功能和/或表达来调节去甲肾上腺素能传递这一概念最初是在20世纪80年代中期被提出的。从那时起,大量研究表明,NET受到多种细胞内和细胞外信号分子的调节,并且NET的磷酸化是调节其细胞表面表达进而调节其功能的主要途径。NET是许多长期用于治疗或长期滥用药物的作用靶点。这推动了众多关于长期接触药物如何调节NET及其功能的研究。虽然已表明反复接触多种药物会影响NET的功能和表达,但这些作用的细胞内机制仍不清楚。

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