Table 2.
Effects of DAT knock-down on striatal DAT and TH-immunoreactivity
striatal DAT-immunoreactivity | ||||||
---|---|---|---|---|---|---|
rostral | medial | caudal | ||||
Age | WT | DAT-KD | WT | DAT-KD | WT | DAT-KD |
Pups (3–4 days) | 1.00 ± 0.10 | 0.54 ± 0.05** | 1.00 ± 0.10 | 0.57 ± 0.05** | 1.00 ± 0.09 | 0.66 ± 0.07* |
aged (18 months) | 1.00 ± 0.09 | 0.42 ± 0.02** | 1.00 ± 0.06 | 0.42 ± 0.04** | 1.00 ± 0.11 | 0.41 ± 0.04** |
striatal TH-immunoreactivity | ||||||
rostral | medial | caudal | ||||
Age | WT | DAT-KD | WT | DAT-KD | WT | DAT-KD |
Pups (3–4 days) | 1.00 ± 0.05 | 1.03 ± 0.05 | 1.00 ± 0.05 | 1.10 ± 0.07 | 1.00 ± 0.04 | 1.16 ± 0.07 |
aged (18 months) | 1.00 ± 0.11 | 0.94 ± 0.09 | 1.00 ± 0.11 | 0.98 ± 0.13 | 1.00 ± 0.13 | 0.88 ± 0.12 |
Striatal DAT and TH immunoreactivity. A coronal section of the rostral, medial and caudal striatum was used for each mouse (pups, WT n=7, DAT-KD =6; 18 months, WT=7, DAT-KD n=7). Data are represented as ratios to respective mean of WT (mean ± SEM) for comparison purposes only; all statistical analyses were performed on raw numbers (2×3 genotype x striatal subregion ANOVA for each age group, Holm-Sidak *p<0.05, **p<0.01 compared to respective WT). Tissue processing and immunohistochemistry for pups and aged mice were performed separately; therefore fluorescence intensities were not compared between ages. Intensity values were not saturated providing similar signal to noise ratio for all age groups.