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Inhibition of hepatic damage and liver fibrosis by brain natriuretic peptide
Authors:Takuhiro Sonoyama  Kazutoshi Miyashita  Kwijun Park  Naofumi Oyamada  Daisuke Taura  Megumi Inuzuka  Yasutomo Fukunaga  Masakatsu Sone  Kazuwa Nakao
Institution:Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
Abstract:Anti-fibrotic and organ protective effects of brain natriuretic peptide (BNP) have been reported. In this study, effects of BNP on liver fibrosis were examined in the carbon tetrachloride (CCl4)-induced liver fibrosis model using BNP-transgenic (Tg) and wild-type (WT) mice. Twice-a-week intraperitoneal injections of CCl4 for 8 weeks resulted in massive liver fibrosis, augmented transforming growth factor (TGF)-β1 and type I procollagen α1 chain (Col1a1) mRNA expression, and the hepatic stellate cell (HSC) activation in WT mice, all of which were significantly suppressed in Tg mice. These observations indicate that BNP inhibits liver fibrosis by attenuating the activation of HSCs.
Keywords:BNP  brain natriuretic peptide  CCl4  carbon tetrachloride  Tg  transgenic  WT  wild-type  TGF  transforming growth factor  Col1a1  type I procollagen α1 chain  HSC(s)  hepatic stellate cell(s) NP  natriuretic peptide  ANP  atrial natriuretic peptide  CNP  C-type natriuretic peptide  GC  guanylyl cyclase  ROS  reactive oxygen species  CYP2E1  cytochrome P450 2E1  NASH  non-alcoholic steatohepatitis  SMA  smooth muscle actin  DMN  dimethylnitrosamine
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