Department of Medicine I, LMU University Hospital, LMU Munich, Munich, Germany.
DZHK (German Centre for Cardiovascular Research), Partner Site Munich, Munich, Germany.
Methods Mol Biol. 2024;2803:163-172. doi: 10.1007/978-1-0716-3846-0_12.
Pulmonary hypertension (PH) is a devastating disease, characterized by complex remodeling of the pulmonary vasculature. PH is classified into five groups based on different etiology, pathology, as well as therapy and prognosis. Animal models are essential for the study of underlying mechanisms, pathophysiology, and preclinical testing of new therapies for PH. The complexity of the disease with different clinical entities dictates the necessity for more than one animal model to resemble PH, as a single model cannot imitate the broad spectrum of human PH.Here we describe a detailed protocol for creating a rat model of PH with right ventricular (RV) failure. Furthermore, we present how to characterize it hemodynamically by invasive measurements of RV and pulmonary arterial (PA) pressures. Animals subjected to this model display severe pulmonary vascular remodeling and RV dysfunction. In this model, rats undergo a single subcutaneous injection of Sugen (SU5416, a vascular endothelial growth factor inhibitor) and are immediately exposed to chronic hypoxia in a hypoxia chamber for 3-6 weeks. This Sugen/Hypoxia rat model resembles Group 1 PH.
肺动脉高压(PH)是一种严重的疾病,其特征是肺血管的复杂重塑。根据不同的病因、病理学以及治疗和预后,PH 分为五组。动物模型对于研究潜在机制、病理生理学以及 PH 的新疗法的临床前测试至关重要。由于不同的临床实体,疾病的复杂性决定了需要不止一种动物模型来模拟 PH,因为单一模型无法模拟广泛的人类 PH。在这里,我们描述了一种创建伴有右心室(RV)衰竭的 PH 大鼠模型的详细方案。此外,我们还介绍了如何通过 RV 和肺动脉(PA)压力的侵入性测量来对其进行血流动力学特征描述。接受该模型的动物表现出严重的肺血管重塑和 RV 功能障碍。在这种模型中,大鼠接受单次皮下注射 Sugen(SU5416,一种血管内皮生长因子抑制剂),并立即在缺氧室中暴露于慢性缺氧 3-6 周。这种 Sugen/低氧大鼠模型类似于第 1 组 PH。