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奥巴库酮通过调节肠道微生物群、减弱TLR4/NF-κB信号级联反应以及改善受损的上皮屏障来保护小鼠免受溃疡性结肠炎的侵害。

Obacunone Protects Against Ulcerative Colitis in Mice by Modulating Gut Microbiota, Attenuating TLR4/NF-κB Signaling Cascades, and Improving Disrupted Epithelial Barriers.

作者信息

Luo Xiaoping, Yue Bei, Yu Zhilun, Ren Yijing, Zhang Jing, Ren Junyu, Wang Zhengtao, Dou Wei

机构信息

Shanghai Key Laboratory of Formulated Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Microbiol. 2020 Mar 31;11:497. doi: 10.3389/fmicb.2020.00497. eCollection 2020.

Abstract

Obacunone, a natural limonoid compound abundantly distributed in citrus fruits, possesses various biological properties, such as antitumor, antioxidant, and antiviral activities. Recent studies suggested an anti-inflammatory activity of obacunone , but its efficacy on intestinal inflammation remains unknown. This study was designed to evaluate the effects and mechanisms of obacunone in ameliorating intestinal inflammation in a mouse model of ulcerative colitis (UC). We found that obacunone efficiently alleviated the severity of dextran sulfate sodium (DSS)-induced mouse UC by modulating the abnormal composition of the gut microbiota and attenuating the excessive activation of toll-like receptor 4 (TLR4)/nuclear factor-kappa B (NF-κB) signaling. The intestinal epithelial barrier was disrupted in DSS colitis mice, which was associated with activation of inflammatory signaling cascades. However, obacunone promoted the expression of tight junction proteins (TJP1 and occludin) and repressed the activation of inflammatory signaling cascades. In summary, our findings demonstrated that obacunone attenuated the symptoms of experimental UC in mice through modulation of the gut microbiota, attenuation of TLR4/NF-κB signaling cascades, and restoration of intestinal epithelial barrier integrity.

摘要

奥巴库酮是一种大量分布于柑橘类水果中的天然柠檬苦素化合物,具有多种生物学特性,如抗肿瘤、抗氧化和抗病毒活性。最近的研究表明奥巴库酮具有抗炎活性,但其对肠道炎症的疗效尚不清楚。本研究旨在评估奥巴库酮在溃疡性结肠炎(UC)小鼠模型中改善肠道炎症的作用及机制。我们发现,奥巴库酮通过调节肠道微生物群的异常组成和减弱Toll样受体4(TLR4)/核因子-κB(NF-κB)信号的过度激活,有效减轻了葡聚糖硫酸钠(DSS)诱导的小鼠UC的严重程度。在DSS结肠炎小鼠中,肠道上皮屏障被破坏,这与炎症信号级联的激活有关。然而,奥巴库酮促进了紧密连接蛋白(TJP1和闭合蛋白)的表达,并抑制了炎症信号级联的激活。总之,我们的研究结果表明,奥巴库酮通过调节肠道微生物群、减弱TLR4/NF-κB信号级联以及恢复肠道上皮屏障完整性,减轻了小鼠实验性UC的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c3/7136403/014fe123f9c8/fmicb-11-00497-g001.jpg

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