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SAMP1/YitFc 小鼠(一种克罗恩病模型)粪便代谢物的疾病进展相关改变。

Disease progression-associated alterations in fecal metabolites in SAMP1/YitFc mice, a Crohn's disease model.

机构信息

Graduate School of Life Science, Hokkaido University, Sapporo, 060-0810, Japan.

Wellness & Nutrition Science Institute, Morinaga Milk Industry Co., Ltd., Zama, Japan.

出版信息

Metabolomics. 2020 Apr 10;16(4):48. doi: 10.1007/s11306-020-01671-5.

Abstract

Crohn's disease (CD) is a chronic, relapsing inflammatory bowel disease affecting the gastrointestinal tract. Although its precise etiology has not been fully elucidated, an imbalance of the intestinal microbiota has been known to play a role in CD. Fecal metabolites derived from microbiota may be related to the onset and progression of CD OBJECTIVES: This study aimed to clarify the transition of gut microbiota and fecal metabolites associated with disease progression using SAMP1/YitFc mice, a model of spontaneous CD METHODS: The ileum tissues isolated from SAMP1/YitFc mice at different ages were stained with hematoxylin-eosin for histologic characterization with CD progression. Feces from control, Institute of Cancer Research (ICR; n = 6), and SAMP1/YitFc (n = 8) mice at different ages were subjected to microbial analysis and H nuclear magnetic resonance (NMR) analysis to investigate fluctuations in gut microbiota and fecal metabolites with CD progression RESULTS: Relative abundance of the Lachnospiraceae, Ruminococcaceae, Bacteroidaceae, and Bacteroidales S24-7 at family-level gut microbiota and fecal metabolites, such as short-chain fatty acids, lactate, glucose, xylose, and choline, dramatically fluctuated with histologic progression of intestinal inflammation in SAMP1/YitFc mice. Unlike the other metabolites, fecal taurine concentration in SAMP1/YitFc mice was higher than ICR mice regardless of age CONCLUSION: The fecal metabolites showing characteristic fluctuations may help to understand the inflammatory mechanism associated with CD, and might be utilized as potential biomarkers in predicting CD pathology.

摘要

克罗恩病(CD)是一种慢性、复发性炎症性肠病,影响胃肠道。尽管其确切病因尚未完全阐明,但肠道微生物群失衡已被认为在 CD 中起作用。源自微生物群的粪便代谢物可能与 CD 的发病和进展有关。

目的

本研究旨在使用 SAMP1/YitFc 小鼠(一种自发性 CD 模型)阐明与疾病进展相关的肠道微生物群和粪便代谢物的转变。

方法

用苏木精-伊红染色对不同年龄的 SAMP1/YitFc 小鼠的回肠组织进行染色,以进行 CD 进展的组织学特征描述。来自对照、癌症研究所(ICR;n = 6)和不同年龄的 SAMP1/YitFc 小鼠(n = 8)的粪便进行微生物分析和 H 磁共振(NMR)分析,以研究与 CD 进展相关的肠道微生物群和粪便代谢物的波动。

结果

在 SAMP1/YitFc 小鼠的肠道微生物群家族水平上,lachnospiraceae、ruminococcaceae、bacteroidaceae 和 bacteroidales S24-7 的相对丰度以及短链脂肪酸、乳酸盐、葡萄糖、木糖和胆碱等粪便代谢物随着肠道炎症的组织学进展而剧烈波动。与其他代谢物不同,无论年龄大小,SAMP1/YitFc 小鼠的粪便牛磺酸浓度均高于 ICR 小鼠。

结论

具有特征性波动的粪便代谢物可能有助于了解与 CD 相关的炎症机制,并可能作为预测 CD 病理学的潜在生物标志物。

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