首页> 美国卫生研究院文献>Frontiers in Medicine >Thin Air Thick Vessels: Historical and Current Perspectives on Hypoxic Pulmonary Hypertension
【2h】

Thin Air Thick Vessels: Historical and Current Perspectives on Hypoxic Pulmonary Hypertension

机译:稀薄的空气厚的血管:低氧性肺动脉高压的历史和当前观点

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The association between pulmonary hypertension (PH) and hypoxia is well-established, with two key mechanistic processes, hypoxic pulmonary vasoconstriction and hypoxia-induced vascular remodeling, driving changes in pulmonary arterial pressure. In contrast to other forms of pulmonary hypertension, the vascular changes induced by hypoxia are reversible, both in humans returning to sea-level from high altitude and in animal models. This raises the intriguing possibility that the molecular drivers of these hypoxic processes could be targeted to modify pulmonary vascular remodeling in other contexts. In this review, we outline the history of research into PH and hypoxia, before discussing recent advances in our understanding of this relationship at the molecular level, focussing on the role of the oxygen-sensing transcription factors, hypoxia inducible factors (HIFs). Emerging links between HIF and vascular remodeling highlight the potential utility in inhibiting this pathway in pulmonary hypertension and raise possible risks of activating this pathway using HIF-stabilizing medications.
机译:肺动脉高压(PH)与低氧之间的关联已得到很好的确立,其存在两个关键的机械过程,即低氧性肺血管收缩和低氧引起的血管重塑,从而驱动肺动脉压的变化。与其他形式的肺动脉高压相反,由缺氧引起的血管变化是可逆的,无论是从高海拔返回海平面的人类还是在动物模型中。这就提出了一种有趣的可能性,即在其他情况下,可以将这些低氧过程的分子驱动器作为目标来修饰肺血管重塑。在这篇综述中,我们概述了PH和缺氧的研究历史,然后讨论了在分子水平上对这种关系的理解的最新进展,重点是氧敏感转录因子,缺氧诱导因子(HIF)的作用。 HIF和血管重塑之间的新兴联系突显了抑制肺动脉高压中该途径的潜在效用,并增加了使用HIF稳定药物激活该途径的可能风险。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号