Bicuspid aortic valve hemodynamics does not promote remodeling in porcine aortic wall concavity

Bicuspid aortic valve hemodynamics does not promote remodeling in porcine aortic wall concavity
复制标题

DOI:
10.4330/wjc.v8.i1.89
复制
发表时间:
2016-01-26
影响因子:
1.9
通讯作者:
Sucosky, Philippe
Sucosky, Philippe
中科院分区:
其他
文献类型:
--
作者:
Atkins, Samantha K.;Moore, Alison N.;Sucosky, Philippe

文献摘要

被引文献

相似文献

目的:探讨在无潜在遗传或结构缺陷的情况下,I型左右二叶主动脉瓣(LR-BAV)血流动力学应力在胸升主动脉(AA)瓣口重构中的作用。从正常(非扩张)猪AAs的腹侧切下的组织标本进行48小时的应力环境中使用的剪切应力生物反应器。通过免疫染色和明胶酶谱分析,以基质金属蛋白酶(MMP)的表达和活性为组织重塑的特征。结果:免疫染色半定量结果表明,暴露于TAV和LR-BAV AA WSS的组织组之间MMP-2和MMP-9的表达无显著差异(分别为P = 0.80和P = 0.19)。酶谱光密度法显示MMP-2活性无差异接受TAV AA和LR-BAV AA WSS的组之间的(总活性、活性形式和潜伏形式)(P = 0.08,P = 0.15,P = 0.59)。结论:在I型LR-1的心脏瓣膜中存在的血流动力学应力环境与TAV AA相比,BAV AA不会引起蛋白水解酶表达和活性的任何显著变化。
AIM: To investigate the role of type-I left-right bicuspid aortic valve (LR-BAV) hemodynamic stresses in the remodeling of the thoracic ascending aorta (AA) concavity, in the absence of underlying genetic or structural defects.METHODS: Transient wall shear stress (WSS) profiles in the concavity of tricuspid aortic valve (TAV) and LR-BAV AAs were obtained computationally. Tissue specimens excised from the concavity of normal (nondilated) porcine AAs were subjected for 48 h to those stress environments using a shear stress bioreactor. Tissue remodeling was characterized in terms of matrix metalloproteinase (MMP) expression and activity via immunostaining and gelatin zymography.RESULTS: Immunostaining semi-quantification results indicated no significant difference in MMP-2 and MMP-9 expression between the tissue groups exposed to TAV and LR-BAV AA WSS (P = 0.80 and P = 0.19, respectively). Zymography densitometry revealed no difference in MMP-2 activity (total activity, active form and latent form) between the groups subjected to TAV AA and LR-BAV AA WSS (P = 0.08, P = 0.15 and P = 0.59, respectively).CONCLUSION: The hemodynamic stress environment present in the concavity of type-I LR-BAV AA does not cause any significant change in proteolytic enzyme expression and activity as compared to that present in the TAV AA.