4.7 Article

Costunolide protects against alcohol-induced liver injury by regulating gut microbiota, oxidative stress and attenuating inflammation in vivo and in vitro

期刊

PHYTOTHERAPY RESEARCH
卷 36, 期 3, 页码 1268-1283

出版社

WILEY
DOI: 10.1002/ptr.7383

关键词

alcohol-induced liver injury; costunolide; Dolomiaea souliei; gut microbiota; LPS-TLR4-NF-kappa B signaling pathway; oxidative stress

资金

  1. Chongqing Social Undertaking and Livelihood Security Project [cstc2017shmsA130079]
  2. Key Joint project of Innovation and Application development of Traditional Chinese Medicine of Chongqing Science and Technology Commission
  3. Chongqing Health Commission [2020ZY013997]
  4. China Postdoctoral Science Foundation [2019M653820XB]

向作者/读者索取更多资源

Costunolide derived from Dolomiaea souliei roots has a protective effect against alcohol-induced liver injury by regulating gut microbiota capacities, adjusting oxidative stress and attenuating inflammation. It may be a potential therapeutic agent for the treatment of liver injury.
Costunolide (cos) derived from the roots of Dolomiaea souliei (Franch.), which belongs to the Dolomiaea genus in the family Compositae, exert the anti-inebriation effect mainly by inhibiting the absorption of alcohol in the gastrointestinal tract. However, the protective effect of cos against alcohol-induced liver injury (ALI) remains obscure. The present study was aimed to evaluate the hepatoprotective effects of cos (silymarin was used as positive control) against ALI and its potential mechanisms. MTT was used to examine the effect of cos on the cell viability of L-02 cells. Plasma was separated from blood that used to test the levels of TNF-alpha, IL-6 and IL-12, and LPS while serum separated from blood which used to detect the level of ALT and AST. Liver tissues were obtained for histopathological examination and western blot analysis. Fresh mice feces samples were collected for the detection of bacterial composition. Cos exhibited protective effect against alcoholic-induced liver injury by regulating gut microbiota capacities (higher relative abundance of Firmicutes and Actinobacteria while lower in Bacteroidetes and Proteobacteria), adjusting oxidative stress (reduced the activities of MDA and ROS while promoted SOD, GSH and GSH-PX in L-02 cells) and attenuating inflammation (decreased the levels of ALT, AST, LPS, IL-6, IL-12 and TNF-alpha) via LPS-TLR4-NF-kappa B p65 signaling pathway, which might be an active therapeutic agent for treatment of ALI.

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