Suppr超能文献

参与乳清蛋白减轻地塞米松诱导的肌肉萎缩的肠道微生物群组成

Composition of gut microbiota involved in alleviation of dexamethasone-induced muscle atrophy by whey protein.

作者信息

Qiu JinLing, Cheng Yixing, Deng Yang, Ren Guangxu, Wang Jiaqi

机构信息

Institute of Food and Nutrition Development, Ministry of Agriculture and Rural Affairs of the Reople's Republic of China, Beijing, China.

College of Food Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong, China.

出版信息

NPJ Sci Food. 2023 Nov 1;7(1):58. doi: 10.1038/s41538-023-00235-w.

Abstract

Skeletal muscle atrophy is a condition associated with increased morbidity and mortality. While the concept of the gut-muscle axis has been proposed, the role of gut microbiota in dexamethasone (DEX)-induced skeletal muscle atrophy remains largely unknown, limiting its clinical applications. In this study, we found that administration of DEX caused a shift in the gut microbiota of mice, characterized by an increased ratio of Firmicutes/Bacteroidota and a reduction in alpha diversity. We also identified 480 new operational taxonomic units (OTUs), while 1168 specific OTUs were lost. Our Spearman correlation analysis revealed 28 key taxonomic genera of bacteria that were positively or negatively associated with skeletal muscle strength and weight (r: -0.881 to 0.845, p < 0.05). Moreover, supplementation with whey protein reshaped the gut microbiota structure in DEX-treated mice, making it more similar to that of the control group. Importantly, we further utilized a stepwise regression model to identify two enterotypes capable of predicting skeletal muscle function and weight. Notably, Ileibacterium and Lachnospiraceae_UCG-001 played significant roles in predicting both skeletal muscle function and weight. Our findings suggest that DEX causes shifts in the gut microbiota, which can be reversed by whey protein intervention. The enterotypes identified by our stepwise regression models predict muscle function and weight, underscoring the potential role of gut microbiota in modulating muscle atrophy and emphasizing the therapeutic opportunities of microbiota-altering interventions.

摘要

骨骼肌萎缩是一种与发病率和死亡率增加相关的病症。虽然肠道 - 肌肉轴的概念已被提出,但肠道微生物群在地塞米松(DEX)诱导的骨骼肌萎缩中的作用仍 largely unknown,限制了其临床应用。在本研究中,我们发现给予DEX会导致小鼠肠道微生物群发生变化,其特征是厚壁菌门/拟杆菌门的比例增加以及α多样性降低。我们还鉴定出480个新的可操作分类单元(OTU),同时有1168个特定OTU消失。我们的斯皮尔曼相关性分析揭示了28个关键的细菌分类属,它们与骨骼肌力量和重量呈正相关或负相关(r:-0.881至0.845,p <0.05)。此外,补充乳清蛋白重塑了DEX处理小鼠的肠道微生物群结构,使其更类似于对照组。重要的是,我们进一步利用逐步回归模型鉴定出两种能够预测骨骼肌功能和重量的肠型。值得注意的是,回肠杆菌属和毛螺菌科_UCG - 001在预测骨骼肌功能和重量方面都发挥了重要作用。我们的研究结果表明,DEX会导致肠道微生物群发生变化,而乳清蛋白干预可以逆转这种变化。我们通过逐步回归模型鉴定出的肠型能够预测肌肉功能和重量,强调了肠道微生物群在调节肌肉萎缩中的潜在作用,并突出了改变微生物群干预措施的治疗机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fee/10618183/f2a9bd179758/41538_2023_235_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验