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参附黄方治疗脓毒症小鼠的肠道微生物群和代谢组谱变化

Alterations in the gut microbiome and metabolome profiles of septic mice treated with Shen FuHuang formula.

作者信息

He Shasha, Zhao Chunxia, Guo Yuhong, Zhao Jingxia, Xu Xiaolong, Hu Yahui, Lian Bo, Ye Haoran, Wang Ning, Luo Lianxiang, Liu Qingquan

机构信息

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.

Beijing Institute of Chinese Medicine, Beijing, China.

出版信息

Front Microbiol. 2023 Mar 8;14:1111962. doi: 10.3389/fmicb.2023.1111962. eCollection 2023.

Abstract

Sepsis has a high mortality rate, and treating sepsis remains a significant challenge worldwide. In former studies, our group found that traditional Chinese medicine, Shen FuHuang formula (SFH), is a promising medicine in treating coronavirus disease 2019 (COVID-19) patients with the septic syndrome. However, the underlying mechanisms remain elusive. In the present study, we first investigated the therapeutic effects of SFH on septic mice. To investigate the mechanisms of SFH-treated sepsis, we identified the gut microbiome profile and exploited untargeted metabolomics analyses. The results demonstrated that SFH significantly enhanced the mice's 7-day survival rate and hindered the release of inflammatory mediators, i.e., TNF-α, IL-6, and IL-1β. 16S rDNA sequencing further deciphered that SFH decreased the proportion of and at the phylum level. LEfSe analysis revealed that the treatment of SFH enriched while decreased . Furthermore, serum untargeted metabolomics analysis indicated that SFH could regulate the glucagon signaling pathway, PPAR signaling pathway, galactose metabolism, and pyrimidine metabolism. Finally, we found the relative abundance of , , , , , and were closely related to the enrichment of the metabolic signaling pathways, including L-tryptophan, uracil, glucuronic acid, protocatechuic acid, and gamma-Glutamylcysteine. In conclusion, our study demonstrated that SFH alleviated sepsis by suppressing the inflammatory response and hence reduced mortality. The mechanism of SFH for treating sepsis may be ascribed to the enrichment of beneficial gut flora and modulation in glucagon signaling pathway, PPAR signaling pathway, galactose metabolism, and pyrimidine metabolism. To sum up, these findings provide a new scientific perspective for the clinical application of SFH in treating sepsis.

摘要

脓毒症死亡率很高,在全球范围内,治疗脓毒症仍然是一项重大挑战。在之前的研究中,我们团队发现,中药参附黄方(SFH)在治疗患有脓毒症综合征的2019冠状病毒病(COVID-19)患者方面是一种有前景的药物。然而,其潜在机制仍不清楚。在本研究中,我们首先研究了SFH对脓毒症小鼠的治疗效果。为了探究SFH治疗脓毒症的机制,我们确定了肠道微生物组谱并进行了非靶向代谢组学分析。结果表明,SFH显著提高了小鼠的7天生存率,并抑制了炎症介质即肿瘤坏死因子-α、白细胞介素-6和白细胞介素-1β的释放。16S核糖体DNA测序进一步表明,SFH在门水平上降低了 和 的比例。线性判别分析效应大小(LEfSe)分析显示,SFH治疗使 富集而 减少。此外,血清非靶向代谢组学分析表明,SFH可以调节胰高血糖素信号通路、过氧化物酶体增殖物激活受体(PPAR)信号通路、半乳糖代谢和嘧啶代谢。最后,我们发现 、 、 、 、 和 的相对丰度与包括L-色氨酸、尿嘧啶、葡萄糖醛酸、原儿茶酸和γ-谷氨酰半胱氨酸在内的代谢信号通路的富集密切相关。总之,我们的研究表明,SFH通过抑制炎症反应减轻了脓毒症,从而降低了死亡率。SFH治疗脓毒症的机制可能归因于有益肠道菌群的富集以及对胰高血糖素信号通路以及PPAR信号通路、半乳糖代谢和嘧啶代谢的调节。综上所述,这些发现为SFH在治疗脓毒症的临床应用提供了新的科学视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b723/10030955/d09849160a13/fmicb-14-1111962-g001.jpg

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