BMC Complementary and Alternative Medicine · 2015 · 34 citations · 13 references
MedicinePharmacologyPharmacotherapyExperimental PharmacologyHepatic PharmacotherapyMolecular PharmacologyAntifibrotic TherapyCirrhosisHepatic ImpairmentHepatic PathophysiologyLiver DiseaseLiver PhysiologyCollagen Type I DepositionHepatic Vascular RegulationHistopathological LesionsHypoxia-inducible Factor ActivationHypoxia-inducible Factor SignalingTraditional Chinese MedicineVascular Endothelial Growth FactorVascular Endothelial Growth Factor Receptors
BACKGROUND: Cirrhosis is associated with angiogenesis and disruption of hepatic vascular architecture. Yiguanjian (YGJ) decoction, a prescription from traditional Chinese medicine, is widely used for treating liver diseases. We studied whether YGJ or its ingredients (iYGJ) had an anti-angiogenic effect and explored possible mechanisms underlying this process. METHODS: Cirrhosis was induced with carbon tetrachloride (CCl4) (ip) in C57BL/6 mice for 6 weeks. From week 4 to week 6, cirrhotic mice were randomly divided into four groups: sorafenib-treated, YGJ-treated and iYGJ-treated mice and placebo. Serum biochemistries, hydroxyproline (Hyp) content and histopathological changes of hepatic tissues were measured as were α-smooth muscle actin (α-SMA), collagen I, CD31, vascular endothelial growth factor (VEGF), VEGF receptor (VEGFR) 2 and hypoxia-inducible factor (HIF)-1α. RESULTS: Both YGJ and iYGJ improved serum biochemistries. Changes of histopathology showed that YGJ and iYGJ reduced hepatic tissue necroinflammatory and collagen fiber deposition in cirrhosis mice. Compared to the CCl4 treated animals, Hyp, α-SMA, collagen I, CD31, VEGF, VEGFR, and HIF-1α expression decreased in YGJ and iYGJ groups. CONCLUSIONS: YGJ and iYGJ inhibited liver angiogenesis in cirrhotic mice treated with CCl4 by inhibiting the HIF-1α/VEGF signaling pathway, suggesting that anti-angiogenic effects of YGJ and iYGJ are associated with improving the hepatic hypoxic microenvironment.
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The Role of Smad3 in Mediating Mouse Hepatic Stellate Cell Activation
Bernd Schnabl, Young Oh Kweon, Joshua P. Frederick et al. · Hepatology · 2001 · 254 citations · Full text