首页> 外文期刊>European journal of applied physiology >Blood pressure regulation VIII: Resistance vessel tone and implications for a pro-atherogenic conduit artery endothelial cell phenotype
【24h】

Blood pressure regulation VIII: Resistance vessel tone and implications for a pro-atherogenic conduit artery endothelial cell phenotype

机译:血压调节VIII:阻力血管张力及其对促动脉粥样硬化导管动脉内皮细胞表型的影响

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Dysfunction of the endothelium is proposed as the primary initiator of atherosclerotic peripheral artery disease, which occurs mainly in medium- to large-sized conduit arteries of the lower extremities (e.g., iliac, femoral, popliteal arteries). In this review article, we propose the novel concept that conduit artery endothelial cell phenotype is determined, in part, by microvascular tone in skeletal muscle resistance arteries through both changes in arterial blood pressure as well as upstream conduit artery shear stress patterns. First, we summarize the literature supporting the involvement of sympathetic nerve activity (SNA) and nitric oxide (NO) in the modulation of microvascular tone and arterial blood pressure. We then focus on the role of elevated blood pressure and shear stress profiles in modulating conduit artery endothelial cell phenotype. Last, we discuss findings from classic and emerging studies indicating that increased vascular resistance, as it occurs in the context of increased SNA and/or reduced NO bioavailability, is associated with greater oscillatory shear stress (e.g., increased retrograde shear) in upstream conduit arteries. The ideas put forth in this review set the stage for a new paradigm concerning the mechanistic link between increased microvascular tone and development of conduit artery endothelial dysfunction and thus increased risk for peripheral artery disease. Indeed, a vast amount of evidence supports the notion that excessive blood pressure and oscillatory shear stress are potent pro-atherogenic signals to the endothelium.
机译:内皮功能障碍被认为是动脉粥样硬化性外周动脉疾病的主要诱因,其主要发生在下肢的中型到大型导管动脉(例如,股动脉,pop动脉)。在这篇综述文章中,我们提出了一种新的概念,即导管动脉内皮细胞表型部分是通过动脉血压的变化以及上游导管动脉切应力模式来确定骨骼肌阻力动脉中的微血管张力。首先,我们总结了支持交感神经活动(SNA)和一氧化氮(NO)参与微血管紧张度和动脉血压调节的文献。然后,我们重点研究血压升高和切应力分布在调节导管动脉内皮细胞表型中的作用。最后,我们讨论来自经典和新兴研究的发现,这些发现表明,在SNA增加和/或NO生物利用度降低的情况下发生的血管阻力增加,与上游导管动脉中的更大的振荡剪切应力(例如,逆行剪切力增加)相关。在这篇综述中提出的想法为新的范式奠定了基础,该范式涉及微血管张力增加与导管动脉内皮功能障碍的发展之间的机械联系,从而增加了周围动脉疾病的风险。确实,大量证据支持以下观点:过高的血压和振荡剪切应力是内皮的有效促动脉粥样硬化信号。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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