Autonomous Effects of Shear Stress and Cyclic Circumferential Stretch regarding Endothelial Dysfunction and Oxidative Stress: An ex vivo Arterial Model

被引:25
作者
Thacher, Tyler N. [1 ]
Silacci, Paolo [3 ]
Stergiopulos, Nikos [1 ]
da Silva, Rafaela F. [1 ,2 ,4 ]
机构
[1] Swiss Fed Inst Technol, Lab Hemodynam & Cardiovasc Technol, CH-1015 Lausanne, Switzerland
[2] Univ Geneva, Sch Med, Univ Med Ctr, Dept Neurosci, CH-1211 Geneva, Switzerland
[3] Stn Rech Agroscope Liebefeld, Posieux, Switzerland
[4] Univ Hosp Geneva, Dept Neurosurg, Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
Endothelial dysfunction; Nitrotyrosine; Oxidative stress; Cyclic stretch and shear stress; NITRIC-OXIDE SYNTHASE; WALL; ATHEROSCLEROSIS; MECHANISMS; CELLS; PHOSPHORYLATION; EXPRESSION; NITRATION; STIFFNESS; DISEASE;
D O I
10.1159/000265567
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Cyclic circumferential stretch and shear stress caused by pulsatile blood flow work in concert, yet are very different stimuli capable of independently mediating endothelial function by modulating eNOS expression, oxidative stress (via production of superoxide anion) and NO bioavailability. Porcine carotid arteries were perfused using an ex vivo arterial support system for 72 h. Groups we created by combining normal (5%) and reduced (1%) stretch with high shear (6 +/- 3 dynes/cm(2)) and oscillatory shear (0.3 +/- 8 3 dynes/cm2) stress while maintaining a pulse pressure of 80 +/- 10 mm Hg. Oscillatory flow and reduced stretch both proved detrimental to endothelial function, whereas oscillatory flow alone dominated total endogenous vascular wall superoxide anion production. Yet, when superoxide anion production was analyzed in just the endothelial region, we observed that it was modulated more significantly by reduced cyclic stretch than by oscillatory shear, emphasizing an important distinction between shear-and stretch-mediated effects to the vascular wall. Western blotting analysis of eNOS and nitrotyrosine proved that they too are more significantly negatively modulated by oscillatory flow than by reduced stretch. These findings point out how shear and stretch stimulate regions of the vascular wall differently, affecting NO bioavailability and contributing to vascular disease. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:336 / 345
页数:10
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