Walter Brendel Center for Experimental Medicine (WBex), University Clinic Munich, LMU Munich, 81377 Munich, Germany.
Center for Cardiovascular Research (DZHK), Munich Heart Alliance (MHA), Partner Site Munich, 81377 Munich, Germany.
Int J Mol Sci. 2023 Mar 2;24(5):4870. doi: 10.3390/ijms24054870.
Pulmonary vein stenosis (PVS) causes a rare type of pulmonary hypertension (PH) by impacting the flow and pressure within the pulmonary vasculature, resulting in endothelial dysfunction and metabolic changes. A prudent line of treatment in this type of PH would be targeted therapy to relieve the pressure and reverse the flow-related changes. We used a swine model in order to mimic PH after PVS using pulmonary vein banding (PVB) of the lower lobes for 12 weeks to mimic the hemodynamic profile associated with PH and investigated the molecular alterations that provide an impetus for the development of PH. Our current study aimed to employ unbiased proteomic and metabolomic analyses on both the upper and lower lobes of the swine lung to identify regions with metabolic alterations. We detected changes in the upper lobes for the PVB animals mainly pertaining to fatty acid metabolism, reactive oxygen species (ROS) signaling and extracellular matrix (ECM) remodeling and small, albeit, significant changes in the lower lobes for purine metabolism.
肺静脉狭窄(PVS)通过影响肺血管内的血流和压力,导致内皮功能障碍和代谢变化,从而引起一种罕见类型的肺动脉高压(PH)。在这种类型的 PH 中,谨慎的治疗方法是靶向治疗以减轻压力并逆转与血流相关的变化。我们使用猪模型通过对下叶肺静脉进行捆绑(PVB)12 周来模拟 PVS 后的 PH,以模拟与 PH 相关的血流动力学特征,并研究为 PH 发展提供动力的分子变化。我们的当前研究旨在对上肺叶和下肺叶进行无偏 proteomic 和 metabolomic 分析,以确定代谢改变的区域。我们发现 PVB 动物的上肺叶主要发生脂肪酸代谢、活性氧(ROS)信号和细胞外基质(ECM)重塑的变化,而下肺叶的嘌呤代谢也发生了微小但显著的变化。