Table 2.
Enzymatic activity analysis.
CTRLm | MOLE 1/1000 | MOLE 1/100 | H2O2 | MOLE 1/1000 ![]() H2O2 |
MOLE 1/100 ![]() H2O2 |
|
---|---|---|---|---|---|---|
SOD a) | 0.35 ± 0.01 | 0.38 ± 0.01 * | 0.44 ± 0.05 * | 0.29 ± 0.02 ** | 0.35 ± 0.03 # | 0.36 ± 0.02 ## |
CAT a) | 3.46 ± 0.16 | 3.92 ± 0.23 * | 4.04 ± 0.09 * | 2.97 ± 0.06 ** | 3.61 ± 0.13 ## | 3.81 ± 0.27 ## |
GPx a) | 368.49 ± 27.48 | 468.20 ± 50.01 * | 483.92 ± 31.65 * | 312.27 ± 17.17 ** | 407.63 ± 16.34 ## | 432.13 ± 22.66 * ## |
GST a) | 144.07 ± 6.54 | 160.26 ± 6.49 * | 168.92 ± 3.75 * | 123.31 ± 2.61 ** | 150.85 ± 5.74 ## | ± 10.94 ## |
SOD, superoxide dismutase; CAT, catalase; GPx, glutathione peroxidase; GST, glutathione transferase. C2C12 myotubes were treated with MOLE stock solution dilutions (1/1000 and 1/100 working solution) or vehicle (methanol) in culture media for 24 h. Then, hydrogen peroxide (1 mM) was added to samples pre-treated with vehicle or MOLE for a further hour. After treatments, the cells were lysed and then cell lysates were used for biochemical analysis. Data presented are the means ± S.D. of three experiments performed in triplicate. a) U/mg proteins. * p < 0.05 and ** p < 0.01 vs. CTRLm; # p < 0.05 and ## p < 0.01 vs. H2O2.