4.7 Article

Sanhuang xiexin decoction ameliorates secondary liver injury in DSS-induced colitis involve regulating inflammation and bile acid metabolism

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 299, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2022.115682

Keywords

Secondary liver injury; UC; Sanhuang Xiexin decoction; Cholestasis; NF-kappa B

Funding

  1. National Natural Science Foundation of China [82004041, 81903812]

Ask authors/readers for more resources

SanHuang XieXin decoction (SXD) is a potential traditional Chinese medicine for treating liver damage secondary to ulcerative colitis (UC), which may work through regulating the gut-liver axis, inhibiting inflammation, and modulating bile acid metabolism pathways.
Ethnopharmacological relevance: SanHuang XieXin decoction (SXD) is a widely applicated traditional Chinese medicine (TCM) with a significant gut-liver axis regulation effect. Aim of the study: To evaluate the therapeutic effect and elucidate the possible underlying molecular mechanisms of SXD on liver damage secondary to ulcerative colitis (UC) in mice. Materials and methods: A model of liver damage secondary to UC was induced by drinking 5% dextran sodium sulfate (DSS) in mice. These mice were treated with one of three doses of SXD or sulfasalazine (SASP), then liver samples were collected and tested. Results: The results reveal that SXD treatment reduced liver cells swelling, and inhibited the accumulation of the hepatic-pro-inflammatory cytokines IL-1 beta and tumor necrosis factor-alpha (TNF-alpha) in mice with colitis. In addition, SXD reduced the production of nitric oxide (NO) and malondialdehyde (MDA), and increased the activities of superoxide dismutase (SOD). In inflammation regulating, SXD significantly down regulated the protein expres-sion of MyD88 and p-I kappa alpha, but upregulated I kappa alpha. In bile acid metabolism regulating, SXD significantly down regulated the protein expression of FXR, MRP2, BESP and SHP. Therefore, SXD treatment can regulate the TLR4-NF-kappa B and bile acid metabolism pathways to alleviate liver inflammation and cholestasis. Conclusions: These results demonstrate that SXD is a potential alternative therapeutic medicine for the treatment of liver damage secondary to colitis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available