Fig. 4. Human insulin dose-dependently induced hydrogen peroxide synthesis in
A. stephensi MSQ43 cells. MSQ43 cells were stimulated with human
insulin (Ins, 0.17–17 µmol l–1) and assayed for
H2O2 using DCF-DA. Controls included no treatment (No
TX), treatment with an equivalent volume of insulin buffer (Hepes), treatment
with 100 units ml–1 catalase (CAT), treatment with 500
µmol l–1 H2O2, and pre-treatment
with catalase (+CAT) followed by treatment with H2O2 or
insulin. Data are represented as mean relative fluorescence units ±
s.e.m. (N=3). An asterisk denotes a significant difference
(
=0.05) between treatment and no treatment (No TX).