1.Effect of Saikokeishito, a Kampo medicine, on hydrogen peroxide-induced premature senescence of normal human dermal fibroblasts.
Takanobu TAKATA ; Yoshiharu MOTOO ; E-mail: MOTOO@KANAZAWA-MED.AC.JP. ; Naohisa TOMOSUGI
Journal of Integrative Medicine 2014;12(6):495-503
OBJECTIVESaikokeishito (TJ-10) is a Kampo (traditional Japanese herbal) medicine, clinically used for hundreds of years in East Asia. Among its various mechanisms elucidated so far, TJ-10 inhibits the production of transforming growth factor-β1 (TGF-β1) and development of pancreatic fibrosis in vivo. Oxidative damage of normal human dermal fibroblasts (NHDFs) in the corium is a cause of human dermal senescence. Our aim was to determine whether TJ-10 protects NHDFs from premature senescence by hydrogen peroxide (H₂O₂).
METHODSPremature senescence was induced in NHDFs by 200 μmol/L H₂O₂ for 4 h. Cell viability and the expressions of p53, AMP-activated protein kinase α1 (AMPKα1), AMPKα2, and 14-3-3 protein sigma (14-3-3 σ) were measured in NHDFs treated with TJ-10 for 48 h before exposure to H₂O₂for 4 h.
RESULTSCell viability after treatment with 200 μmol/L H₂O₂ for 4 h was similar (about 80%) to after pre-treatment with TJ-10. Ascorbic acid as a control did not protect NHDFs from damage by 200 μmol/L H₂O₂. Treatment with 200 μmol/L H₂O₂tended to up-regulate p53 and to down-regulate SIRT1 and AMPKα1, but had no effect on AMPKα2 and 14-3-3 σ expression. Pretreatment with TJ-10 inhibited H₂O₂-induced up-regulation of p53 and enhanced AMPKα1 expression.
CONCLUSIONIt is suggested that Saikokeishito has a protective effect on oxidative stress-induced senescence of NHDFs.
AMP-Activated Protein Kinases ; metabolism ; Antioxidants ; pharmacology ; Ascorbic Acid ; pharmacology ; Cell Culture Techniques ; Cell Survival ; drug effects ; Cellular Senescence ; drug effects ; Dermis ; metabolism ; Down-Regulation ; drug effects ; Drugs, Chinese Herbal ; pharmacology ; Fibroblasts ; metabolism ; Humans ; Hydrogen Peroxide ; pharmacology ; Medicine, Kampo ; methods ; Sirtuin 1 ; metabolism ; Up-Regulation ; drug effects