Mechanism of Resistance Artery Contraction

动脉收缩阻力机制

• 批准号: 6688291
• 负责人: JOSEPH ELLIOTT BRAYDEN
• 金额: $ 34.09万
• 依托单位: UNIVERSITY OF VERMONT & ST AGRIC COLLEGE
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-04-01 至 2005-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6688291
• 关键词: antisense nucleic acid; biological signal transduction; calcium channel; calcium flux; cell morphology; cerebral artery; cerebrovascular system; confocal scanning microscopy; fluorescent dye /probe; laboratory rat; membrane potentials; phospholipase C; protein tyrosine kinase; tissue /cell culture; vascular resistance; vascular smooth muscle; vasoconstriction; voltage /patch clamp; voltage gated channel

Pressure-induced (myogenic) tone is a physiological response centrally involved in autoregulation of blood flow in the brain. A fundamental mechanism involved in the regulation of cerebral artery constriction is depolarization of the smooth muscle cell membrane and increased Ca2+ entry. We have recently identified a cerebrovascular cation channel that could play a major role in both the depolarization and Ca2+-entry processes. Additional preliminary data indicate that this cation channel may be a member of the mammalian transient receptor potential (Trp) family. In the proposed studies, we will characterized the properties of these channels and determine their functional roles in the cerebral circulation. Specific Aim 1. To elucidate the biophysical and pharmacological properties of cation channels activated by cell swelling or increased pressure in cerebrovascular smooth muscle cells and the signal transduction pathways involved in their regulation. These experiments will provide evidence that will establish the role of these channels in pressure-induced depolarization of cerebral artery myocytes. Specific Aim 2. To establish the presence and functional roles of Trp channels in cerebral artery smooth muscle cells. This aim will determine which of the Trp channels are present in cerebrovascular muscle cells and what physiological roles they serve in cerebral resistance arteries. These studies will be performed using a unique combination of approaches from molecular to whole tissue levels to provide an integrated picture of cerebral artery contractile mechanisms involving membrane potential and regulation of [Ca2+]i. State-of-the-art techniques will be employed including membranes potential, cell Ca2+, and diameter measurements in intact arteries, ion channel and cell Ca2+, measurements in freshly isolated vascular smooth muscle cells, and anti- sense oligodeoxynucleotide strategies to suppress Trp channel function. The proposed studies should significantly advance our understanding of the role of cationic channels in the regulation of vascular tone in the brain and indicate novel targets for agents that could be used to correct pathological alterations in cerebral blood flow.

压力诱导的（肌源性）紧张是一种生理反应，主要涉及脑中血流的自动调节。参与脑动脉收缩调节的基本机制是平滑肌细胞膜的去极化和增加的Ca 2+内流。我们最近发现了一个脑血管阳离子通道，可以发挥重要作用，在去极化和Ca2+进入过程。额外的初步数据表明，该阳离子通道可能是哺乳动物瞬时受体电位（Trp）家族的成员。在拟议的研究中，我们将表征这些通道的特性，并确定它们在脑循环中的功能作用。具体目标1。阐明脑血管平滑肌细胞膨胀或压力升高激活的阳离子通道的生物物理和药理学特性及其调控的信号转导途径。这些实验将提供证据，将建立这些通道的压力诱导的脑动脉肌细胞去极化的作用。具体目标2。建立脑动脉平滑肌细胞色氨酸通道的存在和功能作用。这一目标将确定哪些Trp通道存在于脑血管肌肉细胞中，以及它们在脑阻力动脉中发挥什么样的生理作用。这些研究将使用从分子到整个组织水平的独特方法组合进行，以提供涉及膜电位和[Ca2+]i调节的脑动脉收缩机制的综合图像。将采用最先进的技术，包括完整动脉中的膜电位、细胞Ca2+和直径测量、离子通道和细胞Ca2+、新鲜分离的血管平滑肌细胞中的测量以及抑制Trp通道功能的反义寡脱氧核苷酸策略。拟议的研究应显着推进我们的理解的作用，阳离子通道的调节血管紧张度在大脑中，并指出新的目标，可用于纠正脑血流的病理改变的代理。