Table 1. Effect of PPA and BA on neurotransmitter related gene expression in PC12 cells.
Gene/fold change | 1 mM BA | 6 mM BA | 1 mM PPA | 10 mM PPA |
TH | ↑2.8±0.21 | ↓6.4±0.12 | ↑2.17±0.21 | ↓2.2±0.35 |
DBH | ↑1.4±0.17 | ↓14.5±0.89 | ↑1.2±0.23 | ↓1.8±0.13 |
NPY | ↑2.78±0.35 | ↑5.2±0.64 | 1.02±0.28 | ↑ 1.3±0.35 |
ChrA | ↑1.8±0.15 | ↓3.0±0.48 | ↑1.15±0.11 | ↓0.85±0.12 |
PENK | ↑4.65±0.39 | ↑2.46±0.22 | ↑2.7±0.25 | ↑1.95±0.25 |
GTPCH | 1.02±0.09 | 0.98±0.15 | ↑1.45±0.23 | ↑2.67±0.27 |
PC12 cells were treated with 1 mM PPA, 10 mM PPA, 1 mM BA, 6 mM BA or vehicle for 48 hrs. Total RNA samples were isolated from individual petri dishes (n>6 per experimental group). Northern blot analysis was performed as described in Methods section, using probes specific for rat genes, encoding tyrosine hydroxylase (TH), dopamine beta-hydroxylase (DBH), neuropeptide Y (NPY), Chromogranin A (ChrA), pre-proenkephalin (PENK) and GTP cyclohydrolase (GTPCH). The results are presented as mean ± SEM value relative to the mRNA levels in control, vehicle treated cells. 18S rRNA was used as a house keeping gene for normalization of data.