He Qiaoyu, Shi Yumeng, Xing Hong, Tang Qian, Liu Jing, Li Chunxia, Zhang Han, Zhang Boli, Zhang Junhua, Chen Xiaopeng
State Key Laboratory of Component-Based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Front Pharmacol. 2022 Sep 6;13:922642. doi: 10.3389/fphar.2022.922642. eCollection 2022.
Xuanfei Baidu granule (XFBD) is a recommended patented drug for the prevention and treatment of Corona Virus Disease 2019 (COVID-19), which is approved by the National Medical Products Administration. XFBD suppresses the over-activated immune response caused by inflammatory factor storms in COVID-19 infection. The intestine plays a crucial role in the immune system. The mass spectrometry based fecal metabolomics with 16S rDNA sequencing were combined to evaluate the effects of XFBD on host metabolism and gut microbiome. Short-chain fatty acids (SCFAs) contents in fecal matter were quantified by gas chromatography-mass spectrometry (GC-MS). Plasma samples were used to detect immune and inflammatory levels. The results were verified with a rat model of intestinal disorder. Results indicated that XFBD could increase the immune level of Immunoglobulin A (IgA), Immunoglobulin G (IgG) and Immunoglobulin M (IgM) ( < 0.05). The OPLS-DA analysis results showed that a total of 271 differential metabolites (178 up-regulated and 93 down-regulated) were identified based on the VIP ≥1, < 0.05, FC ≥ 2 and FC ≤ 0.5. The metabolic pathways mainly involved D-Glutamine and D-glutamate metabolism, Arginine biosynthesis, Biotin metabolism, et al. XFBD modified the gut bacteria structure according to the principal component analysis (PCA), that is, 2 phyla, 3 classes, 5 orders, 11 families and 14 genera were significantly different based on taxonomic assignment. In addition, it could partially callback the relative abundance of intestinal microflora in bacterial disorder rats caused by antibiotics. It is suggested that the intervention mechanism of XFBD might be related to the regulation of intestinal flora composition. The evidence obtained in the study provides a useful reference for understanding the mechanism of XFBD.
宣肺败毒颗粒(XFBD)是国家药品监督管理局批准的用于预防和治疗新型冠状病毒肺炎(COVID-19)的推荐专利药物。XFBD可抑制COVID-19感染中炎症因子风暴引起的过度激活的免疫反应。肠道在免疫系统中起着至关重要的作用。将基于质谱的粪便代谢组学与16S rDNA测序相结合,以评估XFBD对宿主代谢和肠道微生物群的影响。粪便中短链脂肪酸(SCFAs)含量通过气相色谱-质谱联用仪(GC-MS)进行定量。采集血浆样本检测免疫和炎症水平。研究结果在大鼠肠道紊乱模型中得到验证。结果表明,XFBD可提高免疫球蛋白A(IgA)、免疫球蛋白G(IgG)和免疫球蛋白M(IgM)的免疫水平(<0.05)。OPLS-DA分析结果显示,基于VIP≥1、<0.05、FC≥2和FC≤0.5,共鉴定出271种差异代谢物(178种上调和93种下调)。代谢途径主要涉及D-谷氨酰胺和D-谷氨酸代谢、精氨酸生物合成、生物素代谢等。根据主成分分析(PCA),XFBD改变了肠道细菌结构,即基于分类学归属,有2个门、3个纲、5个目、11个科和14个属存在显著差异。此外,它可以部分回调抗生素引起的肠道菌群紊乱大鼠肠道微生物群的相对丰度。提示XFBD的干预机制可能与肠道菌群组成的调节有关。该研究获得的证据为理解XFBD的作用机制提供了有用的参考。