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非酒精性脂肪肝疾病小鼠肠道微生物群及其与代谢物的相关性。

The Microbiota and It's Correlation With Metabolites in the Gut of Mice With Nonalcoholic Fatty Liver Disease.

机构信息

College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Laboratory Animal Centre, Southwest Medical University, Luzhou, China.

出版信息

Front Cell Infect Microbiol. 2022 May 27;12:870785. doi: 10.3389/fcimb.2022.870785. eCollection 2022.

Abstract

In recent years, nonalcoholic fatty liver disease (NAFLD) has become the most common liver disease in the world. As an important model animal, the characteristics of gut microbiota alteration in mice with NAFLD have been studied but the changes in metabolite abundance in NAFLD mice and how the gut microbiota affects these intestinal metabolites remain unclear. In this experiment, a mouse model for NAFLD was established by a high-fat diet. The use of 16S rDNA technology showed that while there were no significant changes in the alpha diversity in the cecum of NAFLD mice, the beta diversity changed significantly. The abundance of , , , , and increased significantly in NAFLD mice, while and decreased significantly. Amino acids, lipids, bile acids and nucleotide metabolites were among the 167 significantly different metabolites selected. The metabolic pathways of amino acids, SFAs, and bile acids were significantly enhanced, while the metabolic pathways of PUFAs, vitamins, and nucleotides were significantly inhibited. Through correlation and MIMOSA2 analysis, it is suggested that gut microbiota does not affect the changes of lipids and bile acids but can reduce thiamine, pyridoxine, and promote L-phenylalanine and tyramine production. The findings of this study will help us to better understand the relationship between gut microbiota and metabolites in NAFLD.

摘要

近年来,非酒精性脂肪性肝病(NAFLD)已成为世界上最常见的肝脏疾病。作为一种重要的模式动物,已经研究了 NAFLD 小鼠肠道微生物群改变的特征,但 NAFLD 小鼠中代谢物丰度的变化以及肠道微生物群如何影响这些肠道代谢物仍不清楚。在本实验中,通过高脂肪饮食建立了 NAFLD 小鼠模型。16S rDNA 技术的使用表明,虽然 NAFLD 小鼠盲肠的 alpha 多样性没有显著变化,但 beta 多样性变化显著。在 NAFLD 小鼠中, 、 、 、 、 和 的丰度显著增加,而 和 的丰度显著减少。在 167 种显著不同的代谢物中,有氨基酸、脂类、胆汁酸和核苷酸代谢物。氨基酸、SFAs 和胆汁酸的代谢途径显著增强,而 PUFAs、维生素和核苷酸的代谢途径显著受到抑制。通过相关性和 MIMOSA2 分析,提示肠道微生物群不会影响脂质和胆汁酸的变化,但可以减少硫胺素、吡哆醇,并促进 L-苯丙氨酸和酪胺的产生。本研究的结果将有助于我们更好地理解肠道微生物群与 NAFLD 中代谢物之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a774/9186341/49667a10c01d/fcimb-12-870785-g001.jpg

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