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药对通过调节代谢和肠道菌群减轻葡聚糖硫酸钠诱导的溃疡性结肠炎。

The Herbal Pair Attenuate DSS-Induced Ulcerative Colitis by Modulating Metabolism and Intestinal Flora.

作者信息

Zhu Feifei, Ren Chenhui, Zhou Keli, Huang Xueqing, Mei Mengyu, Niu Haiyan, Ren Shouzhong

机构信息

Department of Pathology, The First Affiliated Hospital and School of Basic Medicine and Life Science Hainan Medical University Haikou China.

Engineering Research Center of Tropical Medicine Innovation and Transformation of Ministry of Education, International Joint Research Center of Human-Machine Intelligent Collaborative for Tumor Precision Diagnosis and Treatment of Hainan Province, Hainan Provincial Key Laboratory of Research and Development on Tropical Herbs, School of Pharmacy Hainan Medical University Haikou China.

出版信息

Food Sci Nutr. 2025 Jul 8;13(7):e70584. doi: 10.1002/fsn3.70584. eCollection 2025 Jul.

Abstract

Ulcerative colitis (UC) is a chronic inflammatory bowel disease in which dysbiosis of the intestinal flora plays a critical role in its pathogenesis. (PH-CC) known for its anti-inflammatory properties and ability to regulate gut microbiota, has been demonstrated to alleviate UC. The aim of this study was to investigate the effects of PH-CC on dysbiosis of intestinal flora and metabolic disorders in dextran sodium sulfate (DSS)-induced UC mice. A UC mouse model was induced using a 3% DSS solution, and histopathological changes in the colon were assessed through hematoxylin and eosin staining. The composition and diversity of the intestinal flora were analyzed using 16S rDNA technology, whereas metabolomics was employed to identify potential differential metabolites and metabolic pathways through multivariate statistical analysis. Pearson correlation analysis was performed between metabolites, inflammatory factors, the NLRP3/Caspase-1 pathway, and differential flora. The results revealed that treatment with PH-CC improved the morphological structure of colon tissue and reduced damage in UC mice, while the model group exhibited significant damage to the crypt structure, exfoliation of the colonic mucosal epithelium, loss of glands, and infiltration of inflammatory cells. Analysis of 16S rDNA sequencing data indicated that PH-CC regulated the DSS-induced changes in gut microbiota, significantly decreasing the abundance of The differential microbiota exhibited a strong correlation with the NLRP3/Caspase-1 pathway and downstream inflammatory factors. Additionally, 27 differential metabolites identified in fecal samples were primarily associated with phenylalanine metabolism and bile secretion, showing a high correlation with the differential microbiota. In conclusion, PH-CC regulates dysbiosis in intestinal flora and metabolic disorders in UC mice by reducing the abundance of specific bacterial groups, thereby alleviating inflammatory damage to the colonic mucosa and improving the overall condition of UC.

摘要

溃疡性结肠炎(UC)是一种慢性炎症性肠病,其中肠道菌群失调在其发病机制中起关键作用。以其抗炎特性和调节肠道微生物群的能力而闻名的(PH-CC)已被证明可缓解UC。本研究的目的是探讨PH-CC对葡聚糖硫酸钠(DSS)诱导的UC小鼠肠道菌群失调和代谢紊乱的影响。使用3% DSS溶液诱导建立UC小鼠模型,并通过苏木精和伊红染色评估结肠的组织病理学变化。使用16S rDNA技术分析肠道菌群的组成和多样性,而代谢组学则通过多变量统计分析来鉴定潜在的差异代谢物和代谢途径。对代谢物、炎症因子、NLRP3/Caspase-1途径和差异菌群进行Pearson相关性分析。结果显示,PH-CC治疗改善了UC小鼠结肠组织的形态结构并减少了损伤,而模型组则表现出隐窝结构的显著损伤、结肠黏膜上皮脱落、腺体丢失和炎症细胞浸润。16S rDNA测序数据的分析表明,PH-CC调节了DSS诱导的肠道微生物群变化,显著降低了 的丰度。差异微生物群与NLRP3/Caspase-1途径和下游炎症因子表现出强相关性。此外,在粪便样本中鉴定出的27种差异代谢物主要与苯丙氨酸代谢和胆汁分泌相关,与差异微生物群显示出高度相关性。总之,PH-CC通过降低特定细菌群的丰度来调节UC小鼠的肠道菌群失调和代谢紊乱,从而减轻结肠黏膜的炎症损伤并改善UC的整体状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25a1/12235573/6bbff3dcb9ec/FSN3-13-e70584-g009.jpg

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