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Maslinic acid protects against lipopolysaccharide/d-galactosamine-induced acute liver injury in mice.
Wang, Yuan-Yuan; Diao, Bao-Zhong; Zhong, Li-Hua; Lu, Bao-Ling; Cheng, Yu; Yu, Lei; Zhu, Li-Ying.
Afiliação
  • Wang YY; Department of Infectious Disease, The Forth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, China.
  • Diao BZ; Department of Pharmaceutical Preparations, Liaocheng People's Hospital and Liaocheng Clinical School of Taishan Medical University, Liaocheng, Shandong 252000, China.
  • Zhong LH; Department of Infectious Disease, The Forth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, China.
  • Lu BL; Department of Infectious Disease, The Forth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, China.
  • Cheng Y; Department of Infectious Disease, The Forth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, China.
  • Yu L; Department of Infectious Disease, The Forth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, China. Electronic address: widedoor@sina.com.
  • Zhu LY; Department of Infectious Disease, The Forth Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, China. Electronic address: zlyhmu_62@yeah.net.
Microb Pathog ; 119: 49-53, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29627448
ABSTRACT
Acute liver injury is a life-threatening syndrome that often caused by hepatocyte damage. In this study, we investigated the protective effects of maslinic acid (MA) on lipopolysaccharide (LPS)/d-galactosamine (D-gal)-induced acute liver injury and clarified its mechanism. Mice acute liver injury model was induced by given LPS and D-gal and MA was given intraperitoneally 1 h before LPS and D-gal. Our results showed that MA protected against liver injury by attenuating liver histopathologic changes, serum AST and ALT levels. The increased inflammatory cytokines TNF-α and IL-6 in serum and liver tissues were also inhibited by MA. The level of MDA and the activity of MPO in liver tissues were up-regulated by LPS/D-gal and dose-dependently inhibited by MA. Furthermore, MA attenuated hepatic NF-κB protein expression and increased hepatic Nrf2 and HO-1 protein expression. Taken together, MA offers a protective role against LPS/D-gal-induced liver injury through suppressing NF-κB and activating Nrf2 signaling pathways.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triterpenos / Lipopolissacarídeos / Doença Hepática Induzida por Substâncias e Drogas / Galactosamina / Fígado Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triterpenos / Lipopolissacarídeos / Doença Hepática Induzida por Substâncias e Drogas / Galactosamina / Fígado Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article