State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, National Center for Respiratory Medicine, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University Guangzhou, Guangzhou, Guangdong, China.
GMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, Guangdong, China.
Bioengineered. 2021 Dec;12(1):5173-5183. doi: 10.1080/21655979.2021.1952365.
The gut microbiota is widely considered to be involved in several diseases, including atherosclerosis, obesity, chronic obstructive pulmonary disease (COPD) and pulmonary arterial hypertension (PAH). This study aimed to determine if changes in the gut microbiome and metabolome play a major role in the early pathogenesis of PAH. Male Wistar rats were injected with monocrotaline (MCT) (55 mg/kg) at day 1 and injected with calcium-sensing receptor (CaSR) antagonist NPS2143 (4.5 mg/kg/d) from days 1 to 21. Fecal samples were obtained. The gut microbiota and metabolome were analyzed by 16S rRNA gene sequencing and mass spectrometry-based analysis to investigate the effect of PAH in this rat model. MCT injection had a marked effect on the composition of the gut microbiota. This finding was further confirmed by metabolomic analysis with identification of several metabolites relevant to the gut microflora. However, NPS2143 partially abrogated this intestinal flora disorder and reversed fecal metabolite abnormalities. In conclusion, our study shows correlations between changes in the gut microbiome and the metabolome in PAH, which are affected by NPS2143.
肠道微生物群被广泛认为与多种疾病有关,包括动脉粥样硬化、肥胖、慢性阻塞性肺疾病(COPD)和肺动脉高压(PAH)。本研究旨在确定肠道微生物群和代谢组的变化是否在 PAH 的早期发病机制中起主要作用。雄性 Wistar 大鼠在第 1 天注射单环孢菌素(MCT)(55mg/kg),并在第 1 天至第 21 天每天注射钙敏感受体(CaSR)拮抗剂 NPS2143(4.5mg/kg/d)。获得粪便样本。通过 16S rRNA 基因测序和基于质谱的分析来分析肠道微生物群和代谢组,以研究该大鼠模型中 PAH 的影响。MCT 注射对肠道微生物群的组成有显著影响。代谢组学分析进一步证实了这一发现,鉴定了几种与肠道微生物群相关的代谢物。然而,NPS2143 部分阻断了这种肠道菌群紊乱,并逆转了粪便代谢物异常。总之,我们的研究表明 PAH 中肠道微生物组和代谢组的变化之间存在相关性,这些变化受 NPS2143 的影响。