IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-02-20 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1497563
Yanyan Chen, Jing Zhang, Xiaoran Hou, Shijiao Cai, Jingyue Zhang, Yidan Gou, Hanxu Zhang, Yang Zhai, Hengjie Yuan
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引用次数: 0

摘要

简介复方中药杏诺九丹片(XNJT)已被应用于治疗脑血栓或脑出血后遗症、短暂性脑缺血、视网膜中央静脉阻塞等,但其潜在机制尚不清楚。本研究利用肠道微生物群和代谢组学研究,重点探讨 XNJT 对脑缺血再灌注(MCAO/R)损伤的影响:方法:应用高效液相色谱技术鉴定了 XNJT 的主要成分。我们建立了小鼠 MCAO/R 模型,并进行了行为评估、脑血流测量和 TTC 染色。我们使用 ELISA、高通量 16S rDNA 基因测序和代谢组学技术分别检测了炎症因子、微生物种群和代谢物。最后,我们对肠道微生物群和代谢物之间的关系进行了斯皮尔曼相关分析,全面探讨了XNJT缓解脑缺血再灌注损伤的机制:结果:我们发现,XNJT能有效增强神经系统功能,缓解脑梗塞,减少神经细胞死亡,增加脑血流量。此外,XNJT 还能降低 TNF、IL-6 和 IL-1b 等促炎细胞因子的分泌。此外,XNJT 还改善了 MCAO/R 小鼠的肠道微生物群水平,尤其是乳酸杆菌、真菌、志贺氏菌和利吉乳杆菌。此外,XNJT 主要通过甘油磷脂、亚油酸和鞘氨醇脂代谢途径调节肠道中的不同代谢物。斯皮尔曼相关性分析表明,肠道微生物群与各种代谢物之间存在显著关联:总之,我们的研究结果表明,XNJT 可以改善脑缺血再灌注损伤的预后,减轻炎症反应,调节肠道微生物群和不同的代谢物。其潜在机制可能与控制肠道微生物群和新陈代谢有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Xingnao Jiutan tablets modulate gut microbiota and gut microbiota metabolism to alleviate cerebral ischemia/reperfusion injury.

Introduction: Xingnao Jiutan tablets (XNJT), a compound Chinese medicine, have been applied to the treatment of the sequelae of cerebral thrombosis or cerebral hemorrhage, transient cerebral ischemia, and central retinal vein obstruction, etc., but the underlying mechanisms are not yet clear. This research focused on examining the impact of XNJT for cerebral ischemia/reperfusion (MCAO/R) injury, utilizing gut microbiota and metabolomic studies.

Methods: The primary components of XNJT were identified through the application of the HPLC technique. We established a MCAO/ R model in mice and conducted behavioral evaluations, cerebral blood flow measurements, and TTC staining. We used ELISA, high-throughput 16S rDNA gene sequencing, and metabolomics techniques to detect inflammatory factors, microbial populations, and metabolites, respectively. Finally, we performed Spearman correlation analysis to investigate the relationships among gut microbiota and metabolites, comprehensively exploring the mechanisms of XNJT to alleviate cerebral ischemia-reperfusion injury.

Results: We discovered that XNJT effectively enhanced neurological performance, alleviated cerebral infarction, diminished neuronal cell death, and increased cerebral blood flow. Moreover, XNJT downregulated the secretion of pro-inflammatory cytokines like TNF, IL-6, and IL-1b. Additionally, XNJT improved gut microbiota levels in MCAO/R mice, particularly Bacteroides, Firmicutes, Escherichia-Shigella, and Ligilactobacillus. Furthermore, XNJT primarily modulated differential metabolites in the gut through Glycerophospholipid, Linoleic acid, and Sphingolipid metabolism pathways. Spearman correlation analysis revealed significant associations among intestinal microbiota and various metabolites.

Discussion: In summary, our findings suggest that XNJT can improve cerebral ischemia/reperfusion injury outcomes, reduce inflammatory responses, and regulate gut microbiota and differential metabolites. It's possible that the potential mechanisms are connected to controlling gut microbiota and metabolism.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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