Your browser doesn't support javascript.
loading
Dahuang Zhechong pill attenuates CCl4-induced rat liver fibrosis via the PI3K-Akt signaling pathway.
Gong, Zhenghua; Lin, Jiayu; Zheng, Jie; Wei, Liya; Liu, Li; Peng, Yanzhong; Liang, Weicheng; Hu, Guoxin.
Afiliación
  • Gong Z; Department of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, China.
  • Lin J; Department of Gastroenterology, The Eighth Affiliated Hospital Sun Yat-sen University, Shenzhen, China.
  • Zheng J; Department of Traditional Chinese Medicine, Peking University Shenzhen Hospital, Shenzhen, China.
  • Wei L; Department of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, China.
  • Liu L; Department of Ultrasound, Peking University Shenzhen Hospital, Shenzhen, China.
  • Peng Y; Department of Infectious Diseases, Peking University Shenzhen Hospital, Shenzhen, China.
  • Liang W; School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
  • Hu G; Department of Infectious Diseases, Peking University Shenzhen Hospital, Shenzhen, China.
J Cell Biochem ; 121(2): 1431-1440, 2020 02.
Article en En | MEDLINE | ID: mdl-31502329
ABSTRACT
It is well characterized that activated hepatic stellate cells (HSCs) exert critical functions in accelerating the progression of liver fibrosis. Previous studies have indicated that Dahuang Zhechong pill (DHZCP), a traditional Chinese herbal medicine, is capable of inactivating HSCs and thus attenuate the formation of liver fibrosis in rats. However, pharmacological mechanisms of DHZCP in alleviating liver fibrosis remain unclear. This study aims to investigate the antifibrotic role of DHZCP through inhibiting the phosphatidylinositol 3-kinase (PI3K)-protein kinase B (Akt) pathway. DHZCP was found to significantly suppresses extracellular matrix formation and immune cell infiltration, thus alleviating liver fibrosis symptoms in the in vivo model. Moreover, DHZCP reduced serum levels of transforming growth factor ß1 and tumor necrosis factor-α in rats with liver fibrosis. DHZCP treatment remarkably downregulated protein levels of PI3K and phosphorylated Akt, as well as fibrosis markers. In vitro experiments further demonstrated that DHZCP markedly suppressed HSCs proliferation by downregulating PI3K/Akt, which exerted a synergistic effect with the PI3K inhibitor LY294002. To sum up, our results confirmed that DHZCP exerted an antifibrotic effect in the animal model through inactivating the PI3K/Akt pathway, thus protecting rats from liver injury.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Tetracloruro de Carbono / Regulación de la Expresión Génica / Proteínas Proto-Oncogénicas c-akt / Fosfatidilinositol 3-Quinasa / Cirrosis Hepática Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Cell Biochem Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Tetracloruro de Carbono / Regulación de la Expresión Génica / Proteínas Proto-Oncogénicas c-akt / Fosfatidilinositol 3-Quinasa / Cirrosis Hepática Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Cell Biochem Año: 2020 Tipo del documento: Article País de afiliación: China