The Gut Microbiota Mediates the Protective Effects of Spironolactone on Myocardial Infarction.

IF 3.3 4区 生物学 Q2 MICROBIOLOGY
Journal of Microbiology Pub Date : 2024-10-01 Epub Date: 2024-09-03 DOI:10.1007/s12275-024-00164-7
Lu Li, Jian-Yong Sun, Yu-Lin Li, Shi-Wei Zhu, Sheng-Zhong Duan
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引用次数: 0

Abstract

Myocardial infarction (MI) is a type of cardiovascular disease that influences millions of human beings worldwide and has a great rate of mortality and morbidity. Spironolactone has been used as a critical drug for the treatment of cardiac failure and it ameliorates cardiac dysfunction post-MI. Despite these findings, whether there is a relationship between the therapeutic effects of spironolactone and the gut microorganism after MI has not been determined. In our research, we used male C57BL/6 J mice to explore whether the gut microbiota mediates the beneficial function of spironolactone after myocardial infarction. We demonstrated that deletion of the gut microbiota eliminated the beneficial function of spironolactone in MI mice, displaying exacerbated cardiac dysfunction, cardiac infarct size. In addition, the gut microbiota was altered by spironolactone after sham or MI operation in mice. We also used male C57BL/6 J mice to investigate the function of a probiotic in the myocardial infarction. In summary, our findings reveal a precious role of the gut flora in the therapeutic function of spironolactone on MI.

Abstract Image

肠道微生物群介导螺内酯对心肌梗死的保护作用
心肌梗死(MI)是一种影响全球数百万人的心血管疾病,死亡率和发病率都很高。螺内酯一直是治疗心力衰竭的关键药物,它能改善心肌梗死后的心功能障碍。尽管有这些发现,但螺内酯的治疗效果与心肌梗死后肠道微生物之间是否存在关系尚未确定。在我们的研究中,我们使用雄性 C57BL/6 J 小鼠来探讨心肌梗死后肠道微生物群是否介导螺内酯的有益功能。我们的研究表明,在心肌梗死小鼠中,肠道微生物群的缺失消除了螺内酯的有益功能,表现出加剧的心功能障碍和心肌梗死面积。此外,在小鼠进行假性或心肌梗死手术后,螺内酯会改变肠道微生物群。我们还利用雄性 C57BL/6 J 小鼠研究了益生菌在心肌梗死中的功能。总之,我们的研究结果揭示了肠道菌群在螺内酯对心肌梗死的治疗功能中的重要作用。
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来源期刊
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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