Basic Research
Copyright ©2008 The WJG Press and Baishideng.
World J Gastroenterol. Apr 21, 2008; 14(15): 2343-2348
Published online Apr 21, 2008. doi: 10.3748/wjg.14.2343
Figure 1
Figure 1 Scores of pancreatic tissues in three groups (n = 10, mean ± SD). The pathological score of pancreatic tissues was the highest in the AP group (9.2 ± 2.7) and followed by CQCQD group (5.7 ± 1.9) and C group (0.8 ± 1.0), (P < 0.05).
Figure 2
Figure 2 Intracellular [Ca2+]i of pancreatic acini (n = 10, mean ± SD). The fluorescence intensity (FI) of intracellular [Ca2+]i of pancreatic acinar in AP group (138.2 ± 23.1) was higher than C group (111.0 ± 18.4) and CQCQD group (118.7 ± 15.2 , P < 0.05), but there was no statistical difference between the C group and the CQCQD group (P > 0.05).
Figure 3
Figure 3 Agar gel electrophoresis photograph of PCR products of SERCA1 mRNA. The PCR products of sarcoplasmic reticulum Ca2+-ATPase (SERCA1) mRNA was 199 bp. M: Marker; PC: Positive control with skeletal muscle; C: Control group; A: Acute pancreatitis group; D: Acute pancreatitis group treated with Chaiqinchengqi decoction.
Figure 4
Figure 4 Ct value of GAPDH and SERCA2 mRNA of RT-PCR. Ct: Cycle threshold; G: Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), the internal housekeeping; S: Sarco/endoplasmic reticulum Ca2+-ATPase 2 (SERCA2).
Figure 5
Figure 5 Agar gel electrophoresis photograph of PCR products of SERCA2 mRNA. D: Acute pancreatitis group treated with Chaiqinchengqi decoction; A: Acute pancreatitis group; C: Control group; G: Internal housekeeping gene (GAPDH gene); M: Marker.