Effects
Cells were treated with different concentrations of SAM (0, 0.1, 1 and 10 μM) for 24 h. Cell viability was measured with an MTT assay (A). This expression is expressed as the mean ± SD of the fold- and percent-increases over that of the control. IGF-I mRNA expression was expressed as a fold-increase over that of the control using real-time PCR (B). IGF-1 protein expression was determined using immunoprecipitation and Western blot analysis (C). The mean intensity was measured with densitometry (n=8). Statistical analysis; *p<0.05 and **p<0.05 vs. negative control (control media alone).
Figure 2: Effects of SAM on cell viability and IGF-1 mRNA and protein levels.