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缺氧通过增强短链脂肪酸生成和肠道微生物群重塑来改善耐力表现。

Hypoxia Improves Endurance Performance by Enhancing Short Chain Fatty Acids Production Gut Microbiota Remodeling.

作者信息

Huang Li, Li Tianyou, Zhou Min, Deng Mengyan, Zhang Lidong, Yi Long, Zhu Jundong, Zhu Xiaohui, Mi Mantian

机构信息

Chongqing Key Laboratory of Nutrition and Food Safety, Research Center for Nutrition and Food Safety, Chongqing Medical Nutrition Research Center, Institute of Military Preventive Medicine, Third Military Medical University, Chongqing, China.

出版信息

Front Microbiol. 2022 Feb 7;12:820691. doi: 10.3389/fmicb.2021.820691. eCollection 2021.

DOI:10.3389/fmicb.2021.820691
PMID:35197946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8859164/
Abstract

Hypoxia environment has been widely used to promote exercise capacity. However, the underlying mechanisms still need to be further elucidated. In this study, mice were exposed to the normoxia environment (21% O) or hypoxia environment (16.4% O) for 4 weeks. Hypoxia-induced gut microbiota remodeling characterized by the increased abundance of and genera, and their related short-chain fatty acids (SCFAs) production. It was observed that hypoxia markedly improved endurance by significantly prolonging the exhaustive running time, promoting mitochondrial biogenesis, and ameliorating exercise fatigue biochemical parameters, including urea nitrogen, creatine kinase, and lactic acid, which were correlated with the concentrations of SCFAs. Additionally, the antibiotics experiment partially inhibited hypoxia-induced mitochondrial synthesis. The microbiota transplantation experiment demonstrated that the enhancement of endurance capacity induced by hypoxia was transferable, indicating that the beneficial effects of hypoxia on exercise performance were partly dependent on the gut microbiota. We further identified that acetate and butyrate, but not propionate, stimulated mitochondrial biogenesis and promoted endurance performance. Our results suggested that hypoxia exposure promoted endurance capacity partially by the increased production of SCFAs derived from gut microbiota remodeling.

摘要

缺氧环境已被广泛用于提高运动能力。然而,其潜在机制仍需进一步阐明。在本研究中,将小鼠暴露于常氧环境(21% O₂)或缺氧环境(16.4% O₂)4周。缺氧诱导的肠道微生物群重塑表现为 属和 属丰度增加,以及它们相关的短链脂肪酸(SCFAs)生成。观察到缺氧通过显著延长力竭跑步时间、促进线粒体生物发生以及改善运动疲劳生化参数(包括尿素氮、肌酸激酶和乳酸),显著提高了耐力,这些参数与SCFAs浓度相关。此外,抗生素实验部分抑制了缺氧诱导的线粒体合成。微生物群移植实验表明,缺氧诱导的耐力能力增强是可转移的,这表明缺氧对运动表现的有益作用部分依赖于肠道微生物群。我们进一步确定,乙酸盐和丁酸盐而非丙酸盐刺激线粒体生物发生并促进耐力表现。我们的结果表明,缺氧暴露部分通过肠道微生物群重塑导致的SCFAs生成增加来提高耐力能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/97e34bedf9fc/fmicb-12-820691-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/5b5c24ca74de/fmicb-12-820691-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/07caa0d228ed/fmicb-12-820691-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/bf9090730a1a/fmicb-12-820691-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/e26f127ec8b2/fmicb-12-820691-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/6c6e8883722e/fmicb-12-820691-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/97e34bedf9fc/fmicb-12-820691-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/5b5c24ca74de/fmicb-12-820691-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/07caa0d228ed/fmicb-12-820691-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/bf9090730a1a/fmicb-12-820691-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/e26f127ec8b2/fmicb-12-820691-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/6c6e8883722e/fmicb-12-820691-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436e/8859164/97e34bedf9fc/fmicb-12-820691-g006.jpg

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