结肠炎
肠道菌群
转录组
微生物群
人口
红茶
微分效应
化学
药理学
粪便
微生物学
抗生素
肠道微生物群
生物
食品科学
免疫学
作者
Yina Huang,Yao He,Yunjie Cai,Yu‐Bin Chen,X. Shi,J. He,Kesheng Wu,Hua Wei
出处
期刊:Food & Function
[Royal Society of Chemistry]
日期:2025-10-03
卷期号:17 (3): 1214-1230
摘要
Black tea is commonly used for tea beverage production and has been shown to be an effective natural ingredient to prevent experimentally induced colitis. However, there is limited evidence to show whether black teas of different origins demonstrate similar anti-inflammatory capacity in mice with colitis. In this study, mice were administered daily black tea extracts of lapsang, keemun or dianhong for 1 week prior to receiving 4% dextran sulfate sodium for inducing colitis. Both the lapsang and keemun extracts exhibited better anti-inflammatory effects than dianhong extract, as evidenced by the former two tea extracts enhancing intestinal barrier functions (up-regulation of MUC2 and ZO-1 and increased population of goblet cells) and decreasing colonic and serum pro-inflammatory cytokines. We deduced that gallocatechin (GC) might be a key contributor to the anti-colitis effects of black tea, potentially through synergistic interactions with other components at an optimal ratio to enhance the anti-inflammatory efficacy. Fecal microbiome analysis showed that the gut microbiome was differentially modulated by the lapsang and keemun extracts. Their anti-colitic effects were dependent on the gut microbiome, as shown by the loss of such protection in DSS mice treated with broad-spectrum antibiotics (ABX) for significant microbiome alterations. Mechanistically, colonic transcriptomic analysis showed the differential impacts of lapsang and keemun extracts on colitis via modulating the gene expressions of the glutamatergic synapse and IL-17 pathway, respectively. Further qPCR and immunohistochemistry assays verified the aforementioned pathway modulation. Together, our study provides a roadmap for understanding the effects of different black tea types on colitis and for providing potential directions for the nutritional modulation of colitis.
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