2 × 104 M−1 cm−1 ( Murphy and Kehrer, 1989). The total protein content of lymphocytes was measured by the method of Bradford (Bradford, 1976), using BSA as standard. All data are expressed as mean values and standard errors of at least three independent experiments. Data were analyzed by one-way ANOVA followed by the Tukey’s post hoc test. The software employed for statistical

analyses was GraphPad Prism (version4; GraphPad Software, San Diego, CA, USA). The RG7204 manufacturer functional activity of lymphocytes was assayed by their capacity to proliferate in response to a specific stimulation. Fig. 1 shows the MTT assay results after stimulation with Con A (a T lymphocytes mitogen) or LPS (a B lymphocytes mitogen)

for 48 h. FA at 0.3 mM selleck screening library increased both basal (without stimulation) and LPS-stimulated proliferative capacity of human lymphocytes by 38% and 30%, respectively as compared with non stimulated control group. The addition of astaxanthin to cells treated with FA caused a decrease in the proliferation of lymphocytes in basal, Con A and LPS-stimulated conditions by 43%, 26% and 30%, respectively as compared with 0.3 mM of FA mixture. Intracellular Ca2+ mobilization was significantly enhanced by the mixture of FA in human lymphocytes (about 31-fold) when compared to the control group (Fig. 2). The increase in Ca2+ levels was sustained during 20 min of kinetic monitoring. Treatment with ASTA was unable to prevent the calcium increase induced by FA. BSA (0.2%) addition was able to partially decrease calcium mobilization probably by chelating free FA. To measure intracellular superoxide anion, hydrogen peroxide and nitric oxide production, cells were acutely treated with the FA mixture with or without ASTA as indicated in the material and methods section. As shown in Fig. 3A, the treatment of human lymphocytes with the FA mixture increased the intracellular superoxide

anion levels by 135% as compared with the PMA-control group and as assessed by using fantofarone DHE probe. The addition of ASTA to FA-treated cells promoted a reduction of 20% in superoxide production. Treatment of PMA-control cells with DPI, a NADPH-oxidase inhibitor, totally inhibited superoxide anion production, whereas sodium azide (SA) partially inhibited superoxide anion production. DPI addition in cells treated with fatty acid mixture partially decreased (20%) the superoxide anion production (Fig. 3A). A similar pattern was observed when DCFH-DA probe was used as a general ROS probe (Fig. 3B). An increase of threefold in total ROS production was observed in lymphocytes treated with the FA mixture as compared with PMA-control group. ASTA-treatment decreased the ROS production induced by FA in 20%. Addition of BSA, used as a FA chelating agent, reduced the ROS production in about 32%.