容量过载心力衰竭模型的改进以跟踪心肌重构和器械相关的反向重构。

ISRN cardiology Pub Date : 2011-01-01 Epub Date: 2011-07-06 DOI:10.5402/2011/831062
Egemen Tuzun, Roger Bick, Cihan Kadipasaoglu, Jeffrey L Conger, Brian J Poindexter, Igor D Gregoric, O H Frazier, Jeffrey A Towbin, Branislav Radovancevic
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引用次数: 7

摘要

目的。通过充血性心力衰竭(CHF)和左心室辅助装置(LVAD)的植入治疗,建立绵羊心室重构和反向重构模型。方法。我们诱导了2只羊的容量超负荷心力衰竭;20周后,我们植入LVAD,并在11周后评估恢复情况。我们检查了组织学和血流动力学数据的变化以及CHF细胞标志物的水平。结果。CHF诱导后,我们发现左室舒张末压、左室收缩和舒张尺寸、壁厚、左房内径、心房利钠蛋白(ANP)和内皮素-1 (ET-1)水平升高;β-肾上腺素能受体(BAR)和肌营养不良蛋白的表达明显降低。活检证实左室重构。在LVAD支持后,左室收缩和舒张尺寸、壁厚和质量以及ANP和ET-1水平下降。组织病理学和血流动力学指标改善,BAR和肌营养不良蛋白表达正常化。结论。我们描述了一个成功的绵羊心室和反向重构模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Modification of a volume-overload heart failure model to track myocardial remodeling and device-related reverse remodeling.

Modification of a volume-overload heart failure model to track myocardial remodeling and device-related reverse remodeling.

Modification of a volume-overload heart failure model to track myocardial remodeling and device-related reverse remodeling.

Modification of a volume-overload heart failure model to track myocardial remodeling and device-related reverse remodeling.

Purpose. To provide an ovine model of ventricular remodeling and reverse remodeling by creating congestive heart failure (CHF) and then treating it by implanting a left ventricular assist device (LVAD). Methods. We induced volume-overload heart failure in 2 sheep; 20 weeks later, we implanted an LVAD and assessed recovery 11 weeks thereafter. We examined changes in histologic and hemodynamic data and levels of cellular markers of CHF. Results. After CHF induction, we found increases in LV end-diastolic pressure, LV systolic and diastolic dimensions, wall thickness, left atrial diameter, and atrial natriuretic protein (ANP) and endothelin-1 (ET-1) levels; β-adrenergic receptor (BAR) and dystrophin expression decreased markedly. Biopsies confirmed LV remodeling. After LVAD support, LV systolic and diastolic dimensions, wall thickness, and mass, and ANP and ET-1 levels decreased. Histopathologic and hemodynamic markers improved, and BAR and dystrophin expression normalized. Conclusions. We describe a successful sheep model for ventricular and reverse remodeling.

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