1. Baicalin methyl ester prevents the LPS – induced mice intestinal barrier damage in vivo and in vitro via P65/TNF-α/MLCK/ZO-1 signal pathway
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Mei Liang, Xinyi Sun, Mengru Guo, Huining Wu, Linlu Zhao, Jin Zhang, Jieyi He, Xingbin Ma, Zhichao Yu, Yanhong Yong, Ravi Gooneratne, Xianghong Ju, and Xiaoxi Liu
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Baicalin methyl ester ,Anti-inflammatory ,Intestinal barrier ,TNF-α/MLCK/ZO-1 ,Mice ,MODE-K cells ,Therapeutics. Pharmacology ,RM1-950 - Abstract
The effect of baicalin methyl ester (BME) on the regulation of mice intestinal barrier in the inflammatory response was studied in vivo and in vitro. Thirty six C57/BL mice were randomly divided into six groups (n = 6): control group; LPS group (LPS 3.5 mg/kg given intraperitoneal [ip] on day 7 of the study only), PBS group, and three BME groups (low: 50 mg/kg; medium: 100 mg/kg; high: 200 mg/kg) orally dosed with BME for 7d and LPS ip on day 7. All mice were sacrificed on day 8, and jejunum tissue collected for histopathology (H&E and PAS staining), protein expression of pro-inflammatory factors (TNF-α, IL-6, IL-8, IFN-γ) by ELISA, and intestinal tight junction proteins (ZO-1, occludin, claudin-1 and claudin-4) by Western Blot. Compared with the control group, LPS significantly increased the serum cytokines DAO (p < 0.01) and DLA (p < 0.01), upregulated the expression of pro-inflammatory factors, MLCK proteins (p
- Published
- 2024
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