Key Laboratory of Pulmonary Vascular Medicine and FuWai Hospital, State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Biochemistry, Pharmaceutical College, Henan University, Kaifeng, Henan, China.
Am J Hypertens. 2019 Oct 16;32(11):1109-1117. doi: 10.1093/ajh/hpz121.
Pulmonary arterial hypertension (PAH) is a severe progressive disease with systemic metabolic dysregulation. Monocrotaline (MCT)-induced and hypoxia-induced pulmonary hypertension (PH) rodent models are the most widely used preclinical models, however, whether or not these preclinical models recapitulate metabolomic profiles of PAH patients remain unclear.
In this study, a targeted metabolomics panel of 126 small molecule metabolites was conducted. We applied it to the plasma of the 2 preclinical rodent models of PH and 30 idiopathic pulmonary arterial hypertension (IPAH) patients as well as 30 healthy controls to comparatively assess the metabolomic profiles of PAH patients and rodent models.
Significantly different metabolomics profiling and pathways were shown among the 2 classical rodent models and IPAH patients. Pathway analysis demonstrated that methionine metabolism and urea cycle metabolism were the most significant pathway involved in the pathogenesis of hypoxia-induced PH model and MCT-induced model, respectively, and both of them were also observed in the dysregulated pathways in IPAH patients.
These 2 models may develop PAH through different metabolomic pathways and each of the 2 classical PH model resembles IPAH patients in certain aspects.
肺动脉高压(PAH)是一种严重的进行性疾病,伴有全身代谢失调。野百合碱(MCT)诱导和低氧诱导的肺动脉高压(PH)啮齿动物模型是最广泛使用的临床前模型,但这些临床前模型是否再现 PAH 患者的代谢组学特征尚不清楚。
在这项研究中,我们进行了 126 种小分子代谢物的靶向代谢组学分析。我们将其应用于 2 种 PH 临床前啮齿动物模型和 30 例特发性肺动脉高压(IPAH)患者以及 30 例健康对照者的血浆中,以比较评估 PAH 患者和啮齿动物模型的代谢组学特征。
2 种经典啮齿动物模型和 IPAH 患者之间显示出明显不同的代谢组学特征和途径。途径分析表明,蛋氨酸代谢和尿素循环代谢分别是低氧诱导 PH 模型和 MCT 诱导模型发病机制中最重要的途径,在 IPAH 患者失调的途径中也观察到了这两种途径。
这 2 种模型可能通过不同的代谢组学途径发展为 PAH,并且 2 种经典 PH 模型在某些方面与 IPAH 患者相似。