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结直肠癌小鼠的心脏功能受肠道微生物群远程控制:调节血清代谢物和心肌细胞因子。

Cardiac function of colorectal cancer mice is remotely controlled by gut microbiota: regulating serum metabolites and myocardial cytokines.

作者信息

Gao Zhan-Kui, Fan Chao-Yuan, Zhang Bo-Wen, Geng Jia-Xin, Han Xing, Xu Dan-Qi, Arshad Muhammad, Sun Hao-Xuan, Li Jiong-Yi, Jin Xiangyuan, Mu Xiao-Qin

机构信息

Genomics Research Center (Key Laboratory of Gut Microbiota and Pharmacogenomics of Heilongjiang Province), College of Pharmacy, Harbin Medical University, Harbin, 150081, China.

National Key Laboratory of Frigid Zone Cardiovascular Diseases, Harbin Medical University, Harbin, 150081, China.

出版信息

Anim Microbiome. 2025 May 30;7(1):53. doi: 10.1186/s42523-025-00405-z.

DOI:10.1186/s42523-025-00405-z
PMID:40448218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12123981/
Abstract

Several studies have indicated that the dysregulation of microbial metabolites and the inflammatory environment resulting from microbial dysbiosis may contribute to the occurrence and progression of cardiovascular diseases. Therefore, restoring the disordered gut microbiota in patients with colorectal cancer by fecal microbiota transplantation (FMT) has the potential to reduce the incidence of cardiac disease. In this study, we identified cardiac dysfunction in azomethane and dextran sodium sulfate-induced colorectal cancer mice. Intestinal microbes from healthy mice were transferred to colorectal cancer mice, which vastly reversed the disorder of the gut microbiota and effectively alleviated cardiac dysfunction. Moreover, FMT regulated the expression of serum metabolites such as uridine triphosphate (UTP), tiamulin, andrographolide, and N-Acetyl-D-glucosamine, as well as cytokines like TGF-β, IRF5, and β-MHC in the heart. These findings uncover that the disturbed gut microbiota causes cardiac dysfunction in colorectal cancer mice by modulating the expression of serum metabolites and cytokines, which could be alleviated by treatment with FMT.

摘要

多项研究表明,微生物代谢产物的失调以及微生物群落失衡所导致的炎症环境可能促使心血管疾病的发生与发展。因此,通过粪便微生物群移植(FMT)恢复结直肠癌患者紊乱的肠道微生物群,有可能降低心脏病的发病率。在本研究中,我们在接受偶氮甲烷和葡聚糖硫酸钠诱导的结直肠癌小鼠中发现了心脏功能障碍。将健康小鼠的肠道微生物转移至结直肠癌小鼠体内,这极大地逆转了肠道微生物群的紊乱,并有效缓解了心脏功能障碍。此外,FMT调节了心脏中血清代谢产物如三磷酸尿苷(UTP)、泰妙菌素、穿心莲内酯和N-乙酰-D-葡萄糖胺的表达,以及细胞因子如转化生长因子-β(TGF-β)、干扰素调节因子5(IRF5)和β-肌球蛋白重链(β-MHC)的表达。这些发现揭示,肠道微生物群紊乱通过调节血清代谢产物和细胞因子的表达导致结直肠癌小鼠出现心脏功能障碍,而FMT治疗可缓解这种情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/ce5bccf353c9/42523_2025_405_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/0673a54fe21f/42523_2025_405_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/717fe24999dc/42523_2025_405_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/20ee94e6650c/42523_2025_405_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/ce5bccf353c9/42523_2025_405_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/0673a54fe21f/42523_2025_405_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/717fe24999dc/42523_2025_405_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/20ee94e6650c/42523_2025_405_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e3/12123981/ce5bccf353c9/42523_2025_405_Fig2_HTML.jpg

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本文引用的文献

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Nutrients. 2024 Dec 31;17(1):160. doi: 10.3390/nu17010160.
2
Gut microbiota and risk of endocarditis: a bidirectional Mendelian randomization study.肠道微生物群与心内膜炎风险:一项双向孟德尔随机化研究。
Front Microbiol. 2024 Jan 17;15:1320095. doi: 10.3389/fmicb.2024.1320095. eCollection 2024.
3
A Retrospective Clinical Study on Cardiovascular Complications from Colorectal Cancer.
回顾性研究结直肠癌心血管并发症。
Heart Surg Forum. 2023 Dec 26;26(6):E780-E790. doi: 10.59958/hsf.6733.
4
GlcNac produced by the gut microbiome enhances host influenza resistance by modulating NK cells.肠道微生物组产生的 GlcNac 通过调节 NK 细胞增强宿主对流感的抵抗力。
Gut Microbes. 2023 Dec;15(2):2271620. doi: 10.1080/19490976.2023.2271620. Epub 2023 Nov 12.
5
Fecal microbiota transplantation improves chicken growth performance by balancing jejunal Th17/Treg cells.粪便微生物群移植通过平衡空肠 Th17/Treg 细胞来改善鸡的生长性能。
Microbiome. 2023 Jun 21;11(1):137. doi: 10.1186/s40168-023-01569-z.
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and Improve the IFN Type I-Mediated Antiviral Response in Rotavirus-Infected Cells.并增强轮状病毒感染细胞中I型干扰素介导的抗病毒反应。
Microorganisms. 2023 May 8;11(5):1237. doi: 10.3390/microorganisms11051237.
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