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通过 TRPA1-TRPV1 相互作用调节外周伤害性传递。

Regulation of nociceptive transmission at the periphery via TRPA1-TRPV1 interactions.

机构信息

Department of Endodontics, UTHSCSA, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.

出版信息

Curr Pharm Biotechnol. 2011 Jan 1;12(1):89-94. doi: 10.2174/138920111793937952.

Abstract

TRPV1 and TRPA1 have traditionally been considered to function independently from each other as homomers, but their extensive co-expression in sensory neurons and recent evidence suggest that these channels can functionally interact and may form a complex as part of their normal function. Although TRPA1 and TRPV1 do not absolutely require interaction to maintain function in expression systems or even sensory neurons, their heteromerization may still result in dramatic effects on channel biophysical properties, pharmacology, signaling, regulation, and ultimately function. Understanding the regulation and functional significance of TRPA1-TRPV1 interaction is of tremendous clinical importance since first, both channels are the potential molecular targets for numerous therapeutic drugs; and second, TRPA1-TRPV1 co-expression is far more specific for nociceptive sensory neurons than expression patterns of TRPA1 or TRPV1 considered separately.

摘要

TRPV1 和 TRPA1 传统上被认为作为同源二聚体彼此独立发挥作用,但它们在感觉神经元中的广泛共表达以及最近的证据表明,这些通道可以在功能上相互作用,并可能作为其正常功能的一部分形成复合物。尽管 TRPA1 和 TRPV1 不一定需要相互作用来维持在表达系统或甚至感觉神经元中的功能,但它们的异聚化仍可能对通道的生物物理特性、药理学、信号转导、调节以及最终功能产生显著影响。了解 TRPA1-TRPV1 相互作用的调节和功能意义具有巨大的临床重要性,因为首先,这两个通道都是许多治疗药物的潜在分子靶点;其次,TRPA1-TRPV1 的共表达比单独考虑 TRPA1 或 TRPV1 的表达模式更特异性地针对伤害感受性感觉神经元。

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