Persistent kidney dysfunction in swine renal artery stenosis correlates with outer cortical microvascular remodeling

被引:70
作者
Eirin, Alfonso [1 ]
Zhu, Xiang-Yang [1 ]
Urbieta-Caceres, Victor H. [1 ]
Grande, Joseph P. [1 ,2 ]
Lerman, Amir [3 ]
Textor, Stephen C. [1 ]
Lerman, Lilach O. [1 ,3 ]
机构
[1] Mayo Clin, Div Nephrol & Hypertens, Dept Internal Med, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[3] Mayo Clin, Div Cardiovasc Dis, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
renal hypertension; atherosclerosis; renovascular disease; EXPERIMENTAL RENOVASCULAR DISEASE; BLOOD-FLOW; ISCHEMIC NEPHROPATHY; ANTIOXIDANT VITAMINS; VASCULAR-DISEASE; MEDICAL THERAPY; STENOTIC KIDNEY; INJURY; INTERVENTION; HYPERTENSION;
D O I
10.1152/ajprenal.00697.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Eirin A, Zhu XY, Urbieta-Caceres VH, Grande JP, Lerman A, Textor SC, Lerman LO. Persistent kidney dysfunction in swine renal artery stenosis correlates with outer cortical microvascular remodeling. Am J Physiol Renal Physiol 300: F1394-F1401, 2011. First published March 2, 2011; doi:10.1152/ajprenal.00697.2010.-Percutaneous transluminal renal stenting (PTRS) does not consistently improve renal function in patients with atherosclerotic renovascular disease, but the mechanisms underlying irreversible kidney injury have not been fully elucidated. We hypothesized that renal dysfunction after PTRS is linked to ongoing renal microvascular (MV) remodeling. Pigs were studied after 10 wk of atherosclerosis and renal artery stenosis (ARAS), ARAS treated with PTRS 4 wk earlier, and normal controls (n = 10 each). Renal blood flow (RBF) and glomerular filtration rate (GFR) were studied using multidetector computer tomography. Renal microvascular architecture (micro-CT), angiogenic activity, oxidative stress, and fibrosis were evaluated ex vivo. Four weeks after PTRS, blood pressure was normalized. However, GFR and RBF remained similarly decreased in untreated ARAS and ARAS + PTRS (P < 0.05 vs. normal). MV rarefaction was unaltered after revascularization, and the spatial density of outer cortical microvessels correlated with residual GFR. Interstitial fibrosis and altered expression of proangiogenic and profibrotic factors persisted after PTRS. Tubulointerstitial injury in ARAS persisted 4 wk after mechanically successful PTRS, and vessel loss correlated with residual renal dysfunction. MV loss and fibrosis in swine ARAS might account for persistent renal dysfunction after PTRS and underscore the need to assess renal parenchymal disease before revascularization.
引用
收藏
页码:F1394 / F1401
页数:8
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