Table 2.
Effects of Zinc supplementation on glutathione (GSH) and glutathione sulfide (GSSG) concentrations and GSH:GSSG ratio in choroid plexus epithelial cells (CPECs) exposed to 500 nM CdCl2 for 12 h.
Condition | GSH, µM | GSSG, µM | GSH:GSSG Ratio |
---|---|---|---|
Control | 5.20 ± 0.50 | 0.029 ± 0.010 | 318.4 ± 102.99 |
Cd | 9.18 ± 0.27 * | 0.207 ± 0.023 * | 43.28 ± 5.89 * |
Zn | 5.25 ± 0.46 | 0.035 ± 0.010 | 273.73 ± 99.76 |
Zn + Cd | 7.84 ± 0.87 * | 0.121 ± 0.022 * | 71.94 ± 14.97 * |
CPECs were first incubated for 48 h in maintenance medium without Zinc; i.e., non-supplemented cells, or with 25 µM ZnCl2; i.e., Zn-supplemented cells. Non-supplemented cells were pre-treated (12 h) in serum-free medium (SFM) and then divided into two sets: one set was exposed for 12 h in SFM (Control), while the other was exposed for 12 h to 500 nM CdCl2 in SFM (Cd). In parallel, Zn-supplemented cells were pre-treated (12 h) in SFM with 10 µM ZnCl2 and then divided into two sets: one set was exposed for 12 h in SFM with 10 µM ZnCl2 (Zn), while the other was exposed for 12 h to 500 nM CdCl2 in SFM with 10 µM ZnCl2 (Zn + Cd). All incubations were at 37 °C. GSH and GSSG were analyzed by luminescence in triplicate in four different culture preparations (n = 4); GSH:GSSG ratios were calculated. Data are means ± SE; n = 4 culture preparations. * p < 0.05 vs. Control.