Figure 6

Measurement of intracellular [Ca2+] and [Ca2+] secretory index.
After treatment with 1 mM caffeine for 3-h, intracellular and secretory [Ca2+] contents were measured using a method based on Arsenazo III-calcium reaction (see details in “Materials and Methods”). (A) Intracellular [Ca2+]; (B) [Ca2+] secretory index was calculated using Equation 3: [Ca2+] secretory index = ([Ca2+]Sample Sup − [Ca2+]MEM)/[Ca2+]MEM × 100. Each bar represents mean ± SEM from 3 independent experiments. *p < 0.05 vs. control.