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瞬时受体电位锚蛋白 1 通道对血管张力的调节。

Regulation of vascular tone by transient receptor potential ankyrin 1 channels.

机构信息

Department of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno, School of Medicine, Reno, NV, United States.

Department of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno, School of Medicine, Reno, NV, United States.

出版信息

Curr Top Membr. 2020;85:119-150. doi: 10.1016/bs.ctm.2020.01.009. Epub 2020 Feb 29.

DOI:10.1016/bs.ctm.2020.01.009
PMID:32402637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7656988/
Abstract

The Ca-permeable, non-selective cation channel, TRPA1 (transient receptor potential ankyrin 1), is the sole member of the ankyrin TRP subfamily. TRPA1 channels are expressed on the plasma membrane of neurons as well as non-neuronal cell types, such as vascular endothelial cells. TRPA1 is activated by electrophilic compounds, including dietary molecules such as allyl isothiocyanate, a derivative of mustard. Endogenously, the channel is thought to be activated by reactive oxygen species and their metabolites, such as 4-hydroxynonenal (4-HNE). In the context of the vasculature, activation of TRPA1 channels results in a vasodilatory response mediated by two distinct mechanisms. In the first instance, TRPA1 is expressed in sensory nerves of the vasculature and, upon activation, mediates release of the potent dilator, calcitonin gene-related peptide (CGRP). In the second, work from our laboratory has demonstrated that TRPA1 is expressed in the endothelium of blood vessels exclusively in the cerebral vasculature, where its activation produces a localized Ca signal that results in dilation of cerebral arteries. In this chapter, we provide an in-depth overview of the biophysical and pharmacological properties of TRPA1 channels and their importance in regulating vascular tone.

摘要

钙通透性非选择性阳离子通道,TRPA1(瞬态受体电位锚蛋白 1),是锚蛋白 TRP 亚家族的唯一成员。TRPA1 通道表达于神经元和非神经元细胞类型的质膜上,如血管内皮细胞。TRPA1 被亲电化合物激活,包括膳食分子,如异硫氰酸烯丙酯,芥末的衍生物。内源性的,该通道被认为是由活性氧及其代谢物激活的,如 4-羟基壬烯醛(4-HNE)。在血管系统中,TRPA1 通道的激活导致两种不同机制介导的血管舒张反应。首先,TRPA1 表达于血管的感觉神经中,激活后介导强效扩张剂降钙素基因相关肽(CGRP)的释放。其次,我们实验室的工作表明,TRPA1 仅在脑血管的内皮细胞中表达,其激活产生局部 Ca 信号,导致脑动脉扩张。在本章中,我们提供了 TRPA1 通道的生物物理和药理学特性及其在调节血管张力中的重要性的深入概述。

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本文引用的文献

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Mammalian Transient Receptor Potential TRPA1 Channels: From Structure to Disease.哺乳动物瞬时受体电位 TRPA1 通道:从结构到疾病。
Physiol Rev. 2020 Apr 1;100(2):725-803. doi: 10.1152/physrev.00005.2019. Epub 2019 Oct 31.
2
Atherosclerosis.动脉粥样硬化。
Nat Rev Dis Primers. 2019 Aug 16;5(1):56. doi: 10.1038/s41572-019-0106-z.
3
Knockout of TRPA1 exacerbates angiotensin II-induced kidney injury.敲除 TRPA1 可加重血管紧张素Ⅱ诱导的肾脏损伤。
Am J Physiol Renal Physiol. 2019 Sep 1;317(3):F623-F631. doi: 10.1152/ajprenal.00069.2019. Epub 2019 Jul 24.
4
Neuroprotective effects of TRPA1 channels in the cerebral endothelium following ischemic stroke.TRPA1 通道对缺血性脑卒中后脑血管内皮的神经保护作用。
Elife. 2018 Sep 21;7:e35316. doi: 10.7554/eLife.35316.
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Initial Treatment of Hypertension.高血压的初始治疗
N Engl J Med. 2018 Feb 15;378(7):636-644. doi: 10.1056/NEJMcp1613481.
6
Sites Contributing to TRPA1 Activation by the Anesthetic Propofol Identified by Photoaffinity Labeling.通过光亲和标记鉴定出的麻醉药丙泊酚激活TRPA1的作用位点。
Biophys J. 2017 Nov 21;113(10):2168-2172. doi: 10.1016/j.bpj.2017.08.040. Epub 2017 Sep 19.
7
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