Basic Research
Copyright ©2005 Baishideng Publishing Group Inc.
World J Gastroenterol. May 7, 2005; 11(17): 2583-2590
Published online May 7, 2005. doi: 10.3748/wjg.v11.i17.2583
Figure 1
Figure 1 Comparison of liver pathological changes in three groups of pig serum-induced model rats at wk 10 (A-C), 14 (D-F), 20 (G-I) (Masson 100×).
Figure 2
Figure 2 Comparisons of liver pathologic features in three groups of CCl4-induced model rats at wk 10 (A-C), 14 (D-F), 20 (G-I) (Masson, 100×).
Figure 3
Figure 3 Positive rates of type I collagen (A), α-SMA (B) and TIMP-1 mRNA (C) in pig serum-induced model rats at different time points.
Figure 4
Figure 4 Positive rates of type I collagen (A), α-SMA (B) and TIMP-1 mRNA (C) in CCl4 model rats.
Figure 5
Figure 5 Electron microscopic observation of liver tissues in fibrotic model (A) and prophylaxis model (B).
Figure 6
Figure 6 Dose- and time-dependent effect of Radix Salviae Miltiorrhizae on MDA production (A) and SOD activity (B) at different time points and different concentrations of Radix Salviae Miltiorrhizae root extraction.
Figure 7
Figure 7 HSCs stained by TUNEL (A) and apoptotic cells characterized by compaction of nuclear chromatin and condensation of cytoplasm (B).
Figure 8
Figure 8 Morphological changes of treated HSCs (A) and untreated HSCs (B) with Yi-gan-kang under light microscope.
Figure 9
Figure 9 Ultrastructures of treated HSCs (A) and untreated HSCs (B) with Yi-gan-kang.
Figure 10
Figure 10 Apoptosis rate of HSCs in control group (A) and Yi-gan-kang decoction treatment group (B).