TABLE 5.
Ifenprodil treatment decreased GAD expression and increased phosphorylation of GluN2B.
| Protein | Control | Ifenprodil | 12 h recovery | 24 h recovery | p |
| GluN2B | 1.0 ± 0.06 (6) | 1.05 ± 0.05 (3) | n.d. | 1.04 ± 0.06 (3) | n.s. |
| ph-GluN2B | 1.0 ± 0.04 (10) | n.d. | 1.23 ± 0.052 (5) | 1.26 ± 0.049 (6) | 0.009 |
| GluN1 | 1.0 ± 0.02 (3) | n.d. | 1.04 ± 0.01 (3) | 1.02 ± 0.02 (3) | n.s. |
| PSD-95 | 1.0 ± 0.038 (19) | 1.09 ± 0.041 (6) | 1.034 ± 0.06 (6) | 0.98 ± 0.019 (11) | n.s. |
| GAD-67 | 1.0 ± 0.027 (18) | 0.88 ± 0.02 (6) | 0.89 ± 0.014 (7) | 0.99 ± 0.016 (12) | <0.001 |
| GAD-65 | 1.0 ± 0.016 (18) | 0.78 ± 0.038 (6) | 0.84 ± 0.015 (7) | 0.92 ± 0.013 (12) | <0.001 |
OTC from three preparations were either treated with ifenprodil [10 μM] from DIV 6–10, and harvested at DIV 10 (ifenprodil), or washed two times with fresh medium and maintained for 12 and 24 h (recovery) without ifenprodil. Control cultures were mock-stimulated with water. For the recovery, control cultures were harvested at the 24 h time point. Gel by gel, to generate a S.E.M. also for the controls, control values were normalized to the average of each group of control values which was set to 1; thereafter, all controls were pooled. Reported are the mean ± S.E.M. The number of blots run for every protein/epitope is given in brackets. Statistical comparison was done by ANOVA on ranks versus control; in italics, p-values are given. In bold, values significantly different from control; n.s., not significant; n.d., not determined.