Rapid Communication
Copyright ©2008 The WJG Press and Baishideng.
World J Gastroenterol. Jun 14, 2008; 14(22): 3569-3573
Published online Jun 14, 2008. doi: 10.3748/wjg.14.3569
Figure 1
Figure 1 Light microscopy showing normal liver tissue in the control group (HE staining, × 100) (A), liver fibrosis tissue and formation of more fibrous tissue as well as a large amount of inflammatory cells soaked in intralobules and interlobules in model group (van Gieson staining, × 100) (B), and liver fibrosis tissue in Qianggan-Rongxian Decoction treatment group (C). The pathological change in liver was rather milder compared with the model group (van Gieson staining, × 100).
Figure 2
Figure 2 Electron microscopy showing normal HSC in the model group (A), typical myofibroblasts in the control group (B) (× 5000, bar = 1 &mgr;m), and “transitional” HSC (× 6000, bar = 1 &mgr;m) in Qianggan-Rongxian Decoction treatment group (C).