Fig. 5
DC260126 reversed the inhibitory effect of DHA on cerulein -induced activation of zymogen in AR42J cells. Cells were pretreated with 50 μM of DHA and 10 μM of DC260126 for 2 h and were then stimulated with cerulein (10−8 M) for 2 h. a Trypsin activity was assayed using a fluorogenic assay with a trypsin-specific substrate. Trypsin activity was expressed as milliunits per microgram protein. b The amount of secreted amylase was determined in the media, and total amylase activity was determined in cells using an Amylase Activity Colorimetric Assay kit. Amylase release was expressed as the percentage of secreted amylase/total amylase activity. Data were expressed as the mean ± S.E. of three independent experiments. *p < 0.05 vs. cells without any stimulation or treatment, +p < 0.05 vs. cells with cerulein stimulation alone, ++p < 0.05 vs. cells treated with cerulein and DHA