首页> 美国卫生研究院文献>Journal of Cerebral Blood Flow Metabolism >Isolated human and rat cerebral arteries constrict to increases in flow: role of 20-HETE and TP receptors
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Isolated human and rat cerebral arteries constrict to increases in flow: role of 20-HETE and TP receptors

机译:分离的人和大鼠脑动脉限制流量增加:20-HETE和TP受体的作用

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摘要

Elevation of intraluminal pressure increases vasomotor tone, which thought to have a substantial role in regulation of cerebral blood flow (CBF). Interestingly, responses of cerebral vessels to increases in flow varied and have not been studied in human cerebral arteries. We hypothesized that increases in flow elicit constrictions of isolated human and rat cerebral arteries and aimed to elucidate the underlying mechanisms. Human cerebral arteries and rat middle cerebral arteries constricted to increases in flow (P<0.05). Simultaneous increase in intraluminal flow+pressure further reduced the diameter compared with pressure-induced changes (P<0.05), leading to constant estimated CBF. Flow-induced constrictions were abolished by HET0016 (inhibitor of synthesis of 20-hydroxyeicosatetraenoic acid (20-HETE) or inhibition of COXs or blocking TP (thromboxane A2/prostaglandin H2, receptors and attenuated by scavenging reactive oxygen species (ROS). Flow-enhanced ROS formation was significantly reduced by HET0016. In conclusion, in human and rat cerebral arteries (1) increases in flow elicit constrictions, (2) signaling mechanism of flow-induced constriction of cerebral arteries involves enhanced production of ROS, COX activity, and mediated by 20-HETE via TP receptors, and (3) we propose that simultaneous operation of pressure- and flow-induced constrictions is necessary to provide an effective autoregulation of CBF.
机译:管腔内压力的升高会增加血管舒缩张力,认为这在调节脑血流量(CBF)中起着重要作用。有趣的是,脑血管对血流增加的反应多种多样,尚未在人脑动脉中进行研究。我们假设流量增加会引起人和大鼠孤立的脑动脉收缩,并试图阐明其潜在机制。人脑动脉和大鼠中脑动脉血流量增加(P <0.05)。与压力引起的变化相比,管腔内流量+压力的同时增加进一步减小了直径(P <0.05),导致恒定的估计CBF。 HET0016(20-羟基二十碳四烯酸(20-HETE的合成抑制剂)或COX的抑制或TP(血栓素A2 /前列腺素H2受体)的阻滞剂消除了由流量引起的收缩,并通过清除活性氧(ROS)来减弱。 HET0016显着减少了增强的ROS形成。总之,在人和大鼠脑动脉中(1)血流诱发收缩的增加,(2)血流诱发性脑动脉收缩的信号传导机制涉及ROS的产生增加,COX活性和由20-HETE经由TP受体介导,(3)我们建议同时进行压力和流量引起的收缩对提供有效的CBF自动调节是必要的。

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