Huayu Qutan formula can improve platelet aggregation in acute coronary syndrome rats by regulating gut microbes to drive trimethylamine/flavin containing monooxygenase 3/trimethylamine N-oxide pathway.

Zhang Ni, Chen Yanxi, Jia Lianqun, L I Xinya, M A Yixin
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Abstract

Objective: To investigate the effects of gut microbes regulation of the trimethylamine (TMA)/flavin containing monooxygenase 3 (FMO3)/trimethylamine N-oxide (TMAO) pathway on platelet aggregation in acute coronary syndrome (ACS) rats and the intervention of Huayu Qutan formula.

Methods: The ACS rats with syndrome of phlegm and blood stasis rats were established. Platelet, platelet aggregation, platelet activation markers and TMA/FMO3/ TMAO pathway were detected. Metagenomics technology was employed to analyze the characteristics of the gut microbiota.

Results: Huayu Qutan formula and gut microbes could inhibit high platelet reactivity and regulate the TMA/ FMO3/TMAO pathway. The dominant bacteria in ACS rats including but not limited to the major phyla, Firmicutes, Bacteroidetes, Actinobacteria, and Proteobacteria, also including some low abundance phyla, Fusobacteria, Verrucomicrobia, Spirochaetes, and Deferribacteres. The dominant bacteria in the Huayu Qutan formula group were Synergistetes, Deferribacteres, Deferribacteraceae, Faecalibacterium and Mucispirillum. In the Huayu Qutan formula combined with fecal bacteria enema group, the dominant bacteria were Verrucomicrobia, Verrucomicrobiae, Akkermansia and Verrucomicrobium. These gut microbiota were correlated with pathways such as Riboflavin metabolism and Arachidonic acid metabolism.

Conclusion: Huayu Qutan formula may prevent ACS by modulating gut microbes Synergistetes, Faecalibacterium and Allobaculum, regulating the iron metabolism of Deferribacteres, and driving the TMA/FMO3/TMAO pathway to regulate gut microbiota function, and improving platelet aggregation. Akkermansia may serve as a promising probiotic, which could drive TMA/FMO3/ TMAO pathway to regulate Arachidonic acid metabolism to improve platelet aggregation. The findings of this study provide a theoretical basis for the theory of "the heart is connected with the small intestine".

化瘀祛痰方可通过调节肠道微生物驱动三甲胺/含黄素单加氧酶3/三甲胺n -氧化物途径改善急性冠脉综合征大鼠血小板聚集。
目的:探讨肠道微生物调控三甲胺(TMA)/含黄素单加氧酶3 (FMO3)/三甲胺n -氧化物(TMAO)通路对急性冠脉综合征(ACS)大鼠血小板聚集的影响及化瘀祛痰方的干预作用。方法:建立ACS痰瘀证大鼠模型。检测血小板、血小板聚集、血小板活化标志物及TMA/FMO3/ TMAO通路。采用宏基因组学技术分析肠道菌群特征。结果:化瘀祛痰方和肠道微生物均能抑制血小板高反应性,调节TMA/ FMO3/TMAO通路。ACS大鼠的优势菌群包括但不限于厚壁菌门、拟杆菌门、放线菌门和变形菌门,也包括一些低丰度门、梭菌门、Verrucomicrobia、螺旋体菌门和脱铁菌门。化瘀祛痰方组优势菌群为增效菌属、脱铁杆菌属、脱铁杆菌科、粪杆菌属和粘毛菌属。化瘀祛痰方联合粪菌灌肠组优势菌群为Verrucomicrobia、Verrucomicrobiae、Akkermansia和verrucomicroum。这些肠道菌群与核黄素代谢和花生四烯酸代谢等途径相关。结论:化瘀祛痰方可能通过调节肠道微生物协同菌群、Faecalibacterium和Allobaculum,调节脱铁菌的铁代谢,驱动TMA/FMO3/TMAO通路调节肠道菌群功能,改善血小板聚集来预防ACS。Akkermansia可能是一种很有前景的益生菌,可以通过TMA/FMO3/ TMAO途径调节花生四烯酸代谢,促进血小板聚集。本研究结果为“心小肠通”理论提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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