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肠道微生物代谢产物:连接饮食与动脉粥样硬化的桥梁,以及饮食干预的下一代靶点。

Gut microbial metabolites: The bridge connecting diet and atherosclerosis, and next-generation targets for dietary interventions.

作者信息

Zhang Liyin, Yin Yao, Jin Si

机构信息

Department of Endocrinology, Institute of Geriatric Medicine, Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology, 39 Lake Road, East Lake Ecological Scenic, Wuhan, Hubei 430077, China.

Department of Endocrinology, Institute of Geriatric Medicine, Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology, 39 Lake Road, East Lake Ecological Scenic, Wuhan, Hubei 430077, China.

出版信息

Microbiol Res. 2025 Mar;292:128037. doi: 10.1016/j.micres.2024.128037. Epub 2024 Dec 26.

Abstract

Mounting evidence indicates that gut microbial metabolites are central hubs linking the gut microbiota to atherosclerosis (AS). Gut microbiota enriched with pathobiont bacteria responsible for producing metabolites like trimethylamine N-oxide and phenylacetylglutamine are related to an increased risk of cardiovascular events. Furthermore, gut microbiota enriched with bacteria responsible for producing short-chain fatty acids, indole, and its derivatives, such as indole-3-propionic acid, have demonstrated AS-protective effects. This study described AS-related gut microbial composition and how microbial metabolites affect AS. Summary findings revealed gut microbiota and their metabolites-targeted diets could benefit AS treatment. In conclusion, dietary interventions centered on the gut microbiota represent a promising strategy for AS treatment, and understanding diet-microbiota interactions could potentially be devoted to developing novel anti-AS therapies.

摘要

越来越多的证据表明,肠道微生物代谢产物是将肠道微生物群与动脉粥样硬化(AS)联系起来的核心枢纽。富含产生三甲胺 N-氧化物和苯乙酰谷氨酰胺等代谢产物的致病共生菌的肠道微生物群与心血管事件风险增加有关。此外,富含产生短链脂肪酸、吲哚及其衍生物(如吲哚-3-丙酸)的细菌的肠道微生物群已显示出对 AS 的保护作用。本研究描述了与 AS 相关的肠道微生物组成以及微生物代谢产物如何影响 AS。总结结果表明,针对肠道微生物群及其代谢产物的饮食可能有益于 AS 治疗。总之,以肠道微生物群为中心的饮食干预是一种有前景的 AS 治疗策略,了解饮食与微生物群的相互作用可能有助于开发新的抗 AS 疗法。

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