Basic Research
Copyright ©2005 Baishideng Publishing Group Inc.
World J Gastroenterol. Sep 21, 2005; 11(35): 5492-5497
Published online Sep 21, 2005. doi: 10.3748/wjg.v11.i35.5492
Figure 1
Figure 1 Cardiac myocytes identified by immunocytochemical assay.
Figure 2
Figure 2 Cellular morphological change of cardiomyocytes after exposure to different concentrations of hydrogen peroxide for 4 h. A: Normal control group (magnification ×200); B: cardiomyocytes exposure to 1.25 mmol/L H2O2 (magnification ×200); C: cardiomyocytes exposure to 2.5 mmol/L H2O2 (magnification ×200); D: cardiomyocytes exposure to 5 mmol/L H2O2 (magnification ×200).
Figure 3
Figure 3 Electrophoresis analysis of DNA extracted from cultured myocytes. Lane 1: normal control group; lane 2: 0.625 mmol/L H2O2 for 3 h; lane 3: 1.25 mmol/L H2O2 for 3 h; lane 4: 2.5 mmol/L H2O2 for 3 h; lane 5: 5 mmol/L H2O2 for 3 h; lane 6: 10 mmol/L H2O2 for 3 h; lane 7: DNA marker.
Figure 4
Figure 4 Anti-apoptosis effect of nm-haFGF on cardiomyocytes injured by H2O2.