Table 1. Synaptic protein composition in GluD1 KO mice.
Protein | Amygdala | Prefrontal Cortex | ||||
Ratio | SEM | P | Ratio | SEM | P | |
GluA1 | 2.293 | 0.563 | 0.0486* | 0.508 | 0.056 | <0.001*** |
GluA2 | 0.885 | 0.115 | 0.5686 | 0.528 | 0.198 | 0.0345* |
GluN2B | 1.180 | 0.152 | 0.2780 | 1.770 | 0.478 | 0.1364 |
GluK2 | 1.764 | 0.286 | 0.0327* | 0.930 | 0.060 | 0.4428 |
vGluT2 | 1.087 | 0.258 | 0.7556 | 1.059 | 0.277 | 0.8747 |
GAD67 | 1.269 | 0.111 | 0.0640 | 0.941 | 0.207 | 0.8027 |
PSD95 | 1.601 | 0.146 | 0.0028** | 1.286 | 0.237 | 0.2761 |
Synaptophysin | 1.166 | 0.118 | 0.2905 | 1.049 | 0.196 | 0.8176 |
Synaptoneurosomes were isolated from the GluD1 KO and WT amygdala and prefrontal cortex and western blotting was performed (5–11 animals for each group). Data are presented as mean ± SEM. First, the optical density of each sample was normalized to β-actin. Thereafter, the optical density was normalized to the mean of the WT samples. The average ± SEM of optical densities of GluD1 KO samples, that were normalized to WT mean, are represented as Ratio (KO/WT) ± SEM. The P values were calculated from optical densities of WT and GluD1 KO samples normalized to the WT mean.
represents P<0.001.
represents P<0.01 and.
represents P<0.05.