肠道菌群代谢支链氨基酸及其代谢物可改善衰老小鼠的生理功能。

IF 8 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2024-12-04 DOI:10.1111/acel.14434
Hongchao Wang, Ling Feng, Zhangming Pei, Jianxin Zhao, Shourong Lu, Wenwei Lu
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引用次数: 0

摘要

肠道菌群对支链氨基酸的代谢可以改善整体健康,并可能逆转衰老。在这项研究中,我们研究了副芽孢杆菌merdae,一种已知分解支链氨基酸(BCAAs)的肠道微生物。用三种BCAAs代谢物异戊酸、2-甲基丁酸和异丁酸治疗D-gal诱导的衰老小鼠。结果表明,这些治疗方法可以通过减少氧化应激和炎症、提高肌肉能力、逆转脑乙酰胆碱水平和调节血糖等健康益处来延缓小鼠的衰老。结合肠道微生物群宏基因组和粪便血清代谢组,初步探讨其机制。副芽孢杆菌可改变小鼠肠道菌群的种类组成和结构。增加有益细菌的丰度,如假长双歧杆菌。三种代谢物通过多种信号通路影响肠道菌群和机体蛋白质通路,改善整体健康。综上所述,调节参与支链氨基酸代谢的肠道菌群带来健康益处可能是一种逆转衰老的新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiota metabolism of branched-chain amino acids and their metabolites can improve the physiological function of aging mice.

The metabolism of branched-chain amino acids by gut microbiota can improve overall health and may reverse aging. In this study, we investigated Parabacteroides merdae, a gut microbe that is known to catabolise branched-chain amino acids (BCAAs). Three metabolites of BCAAs isovalerate, 2-methylbutyrate, and isobutyrate were used to treat D-gal induced aging mice. The results showed that these treatments could delay aging in mice by providing health benefits in reducing oxidative stress and inflammation, improving muscle capacity, reversing brain acetylcholine levels, and regulating blood glucose. The mechanism was preliminarily explored by combining the gut microbiota metagenome and faecal serum metabolome. Parabacteroides merdae altered the species composition and structure of the gut microbiota in mice. Increasing the abundance of beneficial bacteria, such as Bifidobacterium pseudolongum. Three metabolites affects the gut microbiota and the body's pathways of protein and improves the overall health through a variety of signaling pathways. Overall, regulating the gut microbiota involved in branched-chain amino acid metabolism to bring health benefits may be a new way of reversing aging.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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