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Traditional Chinese Medicine Yang-Gan-Wan Alleviated Experimental Hepatic Damage by Inhibiting Oxidation, Inflammation, and Apoptosis in Cell and Mouse Models.
Yeh, Chia-Wen; Wu, Wan-Jhen; Lu, Chen-Wen; Wang, Sheue-Er; Chuang, Wu-Chang; Lee, Ming-Chung; Wu, Chung-Hsin.
Afiliação
  • Yeh CW; School of Life Science, National Taiwan Normal University, Taipei City, Taiwan.
  • Wu WJ; School of Life Science, National Taiwan Normal University, Taipei City, Taiwan.
  • Lu CW; School of Life Science, National Taiwan Normal University, Taipei City, Taiwan.
  • Wang SE; Pathological Department, Saint Paul's Hospital, Taoyuan City, Taiwan.
  • Chuang WC; Sun Ten Pharmaceutical Co., Ltd., New Taipei City 23143, Taiwan.
  • Lee MC; Brion Research Institute of Taiwan, New Taipei City 23143, Taiwan.
  • Wu CH; School of Life Science, National Taiwan Normal University, Taipei City, Taiwan.
Article em En | MEDLINE | ID: mdl-34659428
ABSTRACT
A hepatoprotective medicine, Yang-Gan-Wan (YGW), was used to treat hepatic damage in cell and mouse models. We performed a 1,1-diphenyl-2- picrylhydrazyl (DPPH) assay and found that YGW exhibited a significantly high free radical scavenging ability. Furthermore, the results of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay revealed that YGW treatment could alleviate lipopolysaccharide (LPS)-induced damage in Kupffer cells (liver macrophages). Enzyme-linked immunosorbent assay results demonstrated that YGW treatment could alleviate LPS-induced inflammation in Kupffer cells by inhibiting the expression of tumor necrosis factor (TNF)-α and interleukin (IL)-1ß. By quantifying the serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), we found that YGW treatment could alleviate hepatic damage and improve immunity in acetaminophen- (APAP-) treated mice by inhibiting the expression of ALT and AST. The findings of hematoxylin and eosin and Masson's trichrome staining indicated that YGW treatment could alleviate hepatic damage and reduce collagen fiber formation in the liver tissue of APAP-treated mice. Furthermore, immunohistochemistry staining and Western blot results showed that YGW treatment could alleviate oxidative stress, inflammation, and apoptosis in the liver tissue of APAP-treated mice by enhancing superoxide dismutase 2 (SOD2) expression but inhibiting TNF-α and caspase 3 expression. Our results suggest that YGW treatment exerted hepatoprotective effects on LPS-treated Kupffer cells and APAP-treated mice by inhibiting oxidation, inflammation, and apoptosis.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article