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动态绵羊模型诱导肺动脉高压和右心衰竭。

A Dynamic Sheep Model to Induce Pulmonary Hypertension and Right Ventricular Failure.

机构信息

Department of Cardiac Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

Vanderbilt University, Nashville, TN, USA.

出版信息

Methods Mol Biol. 2024;2803:239-258. doi: 10.1007/978-1-0716-3846-0_18.

Abstract

Decompensated right ventricular failure (RVF) in pulmonary hypertension (PH) is fatal, with limited medical treatment options. Developing and testing novel therapeutics for PH requires a clinically relevant large animal model of increased pulmonary vascular resistance and RVF. This manuscript describes the method to induce an ovine PH-RVF model that utilizes left pulmonary artery (LPA) ligation, progressive main pulmonary artery (MPA) banding, and insertion of an RV pressure line for monitoring. The PA cuff and RV pressure tubing are connected to subcutaneous access ports. This model of PH-RVF is a versatile platform to control not only the disease severity, but also the RV's phenotypic response. Subjects undergo progressive PA band adjustments twice per week for approximately 9 weeks with sequential measures of RV pressure, PA cuff pressures, and mixed venous blood gas (SvO). Subjects can further be exercised on a livestock treadmill while hemodynamic parameters are captured. At the initiation and endpoint of this model, ventricular function and dimensions are assessed using echocardiography. In this model, RV mean and systolic pressure increased to 28 ± 5 and 57 ± 7 mmHg at week 1, and further to 44 ± 7 and 93 ± 18 mmHg by week 9, respectively. Echocardiography demonstrates characteristic findings of PH-RVF, notably RV dilation, increased wall thickness, and septal bowing. The rate of PA banding has a significant impact on SvO and thus the model can be titrated to elicit varying RV phenotypes. When the PA cuff is tightened rapidly, it can lead to a precipitous decline in SvO, leading to RV decompensation, whereas a slower, more paced strategy leads to an adaptive RV stress-load response that maintains physiologic SvO. A faster rate of PA banding will also lead to more severe liver fibrosis. The addition of controlled exercise provides a useful platform for assessing the effects of physical exertion in a PH-RVF model. This chronic PH-RVF model provides a valuable tool for studying molecular mechanisms, developing diagnostic biomarkers, and evaluating mechanical circulatory support systems.

摘要

肺动脉高压(PH)所致的右心衰竭(RVF)是致命的,目前治疗方法有限。开发和测试治疗 PH 的新疗法需要一种具有临床相关性的、可增加肺血管阻力和 RVF 的大型动物模型。本文描述了一种诱导绵羊 PH-RVF 模型的方法,该模型利用左肺动脉(LPA)结扎、主肺动脉(MPA)渐进性缩窄以及 RV 压力线插入进行监测。PA 袖带和 RV 压力管连接到皮下接入端口。这种 PH-RVF 模型是一种多功能平台,不仅可以控制疾病严重程度,还可以控制 RV 的表型反应。动物每周接受两次 PA 带渐进性调整,大约 9 周,连续测量 RV 压力、PA 袖带压力和混合静脉血气(SvO)。可以在牲畜跑步机上对动物进行锻炼,同时捕获血流动力学参数。在该模型的开始和结束时,使用超声心动图评估心室功能和尺寸。在该模型中,RV 平均和收缩压分别在第 1 周增加到 28±5 和 57±7mmHg,在第 9 周分别增加到 44±7 和 93±18mmHg。超声心动图显示出 PH-RVF 的特征性发现,尤其是 RV 扩张、壁厚度增加和室间隔弯曲。PA 带缩窄的速度对 SvO 有显著影响,因此可以对模型进行滴定以引起不同的 RV 表型。当快速收紧 PA 袖带时,SvO 会急剧下降,导致 RV 失代偿,而较慢、更有节奏的策略会导致 RV 适应压力负荷反应,从而维持生理 SvO。PA 带缩窄的更快速度也会导致更严重的肝纤维化。控制运动的加入为评估 PH-RVF 模型中体力活动的影响提供了一个有用的平台。这种慢性 PH-RVF 模型为研究分子机制、开发诊断生物标志物和评估机械循环支持系统提供了有价值的工具。

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