Altered hemodynamics, endothelial function, and protein expression occur with aortic coarctation and persist after repair

作者：Menon Arjun; Eddinger Thomas J; Wang Hongfeng; Wendell David C; Toth Jeffrey M; LaDisa John F Jr^*

来源：American Journal of Physiology - Heart and Circulatory Physiology, 2012, 303(11): H1304-H1318.

DOI：10.1152/ajpheart.00420.2012

• vascular remodeling
• contractile protein
• hemodynamics
• endothelial dysfunction
• nonmuscle myosin

Menon A, Eddinger TJ, Wang H, Wendell DC, Toth JM, LaDisa JF Jr. Altered hemodynamics, endothelial function, and protein expression occur with aortic coarctation and persist after repair. Am J Physiol Heart Circ Physiol 303: H1304-H1318, 2012. First published September 28, 2012; doi: 10.1152/ajpheart.00420.2012.-Coarctation of the aorta (CoA) is associated with substantial morbidity despite treatment. Mechanically induced structural and functional vascular changes are implicated; however, their relationship with smooth muscle (SM) phenotypic expression is not fully understood. Using a clinically representative rabbit model of CoA and correction, we quantified mechanical alterations from a 20-mmHg blood pressure (BP) gradient in the thoracic aorta and related the expression of key SM contractile and focal adhesion proteins with remodeling, relaxation, and stiffness. Systolic and mean BP were elevated for CoA rabbits compared with controls leading to remodeling, stiffening, an altered force response, and endothelial dysfunction both proximally and distally. The proximal changes persisted for corrected rabbits despite %26gt;12 wk of normal BP (similar to 4 human years). Computational fluid dynamic simulations revealed reduced wall shear stress (WSS) proximally in CoA compared with control and corrected rabbits. Distally, WSS was markedly increased in CoA rabbits due to a stenotic velocity jet, which has persistent effects as WSS was significantly reduced in corrected rabbits. Immunohistochemistry revealed significantly increased nonmuscle myosin and reduced SM myosin heavy chain expression in the proximal arteries of CoA and corrected rabbits but no differences in SM alpha-actin, talin, or fibronectin. These findings indicate that CoA can cause alterations in the SM phenotype contributing to structural and functional changes in the proximal arteries that accompany the mechanical stimuli of elevated BP and altered WSS. Importantly, these changes are not reversed upon BP correction and may serve as markers of disease severity, which explains the persistent morbidity observed in CoA patients.

• 出版日期2012-12