Suppr超能文献

大鼠坏死性小肠结肠炎模型中肠道微生物群与代谢物的综合分析

Integrated Analysis of Gut Microbiota and Metabolites in a Rat Necrotizing Enterocolitis Model.

作者信息

Lai Panjian, Wang Dayan, Li Xiaobing

机构信息

Department of Pediatrics, Jinhua Maternal and Child Health Care Hospital, Zhejiang , China.

出版信息

Turk J Gastroenterol. 2025 Jan 20;36(5):312-320. doi: 10.5152/tjg.2025.24451.

Abstract

BACKGROUND/AIMS:: Necrotizing enterocolitis (NEC) is a critical gastrointestinal emergency in newborns, characterized by mucosal damage, gut microbial dysbiosis, and inflammation. This study aimed to identify differential gut microbiota and metabolites in NEC and examine their correlations.

MATERIALS AND METHODS

: A rat model of NEC was established using hypoxia–hyperoxia and cold stress. Histopathological analysis, liquid chromatography–mass spectrometry, and 16S rDNA sequencing were used to analyze intestinal contents and tissues. Proinflammatory cytokine concentrations were measured via enzyme-linked immunosorbent assay.

RESULTS

: Necrotizing enterocolitis rats exhibited significant intestinal damage, including hemorrhage, edema, necrosis, and inflammatory infiltration ( < .05). Correlation analysis revealed strong associations between specific microbiota (e.g., and ) and metabolites, suggesting their involvement in NEC pathogenesis ( < .05). Furthermore, NEC rats had elevated proinflammatory cytokine levels, including interleukin-1β, tumor necrosis factor-α, and interleukin-6 ( < .05).

CONCLUSION

: This study successfully established a rat model of NEC, highlighting key microbiota–metabolite correlations and increased proinflammatory cytokines, providing insights into NEC pathogenesis and potential therapeutic targets.

摘要

背景/目的:坏死性小肠结肠炎(NEC)是新生儿严重的胃肠道急症,其特征为黏膜损伤、肠道微生物群失调和炎症。本研究旨在鉴定NEC中肠道微生物群和代谢物的差异,并研究它们之间的相关性。

材料与方法

采用缺氧-高氧和冷应激建立NEC大鼠模型。利用组织病理学分析、液相色谱-质谱联用技术和16S rDNA测序分析肠道内容物和组织。通过酶联免疫吸附测定法测量促炎细胞因子浓度。

结果

坏死性小肠结肠炎大鼠表现出明显的肠道损伤,包括出血、水肿、坏死和炎症浸润(P<0.05)。相关性分析显示特定微生物群(如……和……)与代谢物之间存在密切关联,表明它们参与了NEC的发病机制(P<0.05)。此外,NEC大鼠的促炎细胞因子水平升高,包括白细胞介素-1β、肿瘤坏死因子-α和白细胞介素-6(P<0.05)。

结论

本研究成功建立了NEC大鼠模型,突出了关键的微生物群-代谢物相关性以及促炎细胞因子的增加,为NEC的发病机制和潜在治疗靶点提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfb/12070429/caffba126d48/tjg-36-5-312_f001.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