Table 1.
WT + vehicle | WT + 25(OH)D3 + 1,25(OH)2D3 | Ctns−/− + vehicle | Ctns−/− + 25(OH)D3 + 1,25(OH)2D3 | |
---|---|---|---|---|
n = 8 | n = 8 | n = 8 | n = 8 | |
BUN (mg/dL) | 32.4 ± 5.5 | 32.5 ± 3.8 | 79.6 ± 14.6a | 80.2 ± 9.8a |
Ca (mg/dL) | 11.2 ± 0.6 | 11.3 ± 0.8 | 9.1 ± 0.5b | 10.6 ± 0.4 |
Creatinine (mg/dL) | <0.2 ± 1.1 | 0.3 ± 0.2 | 0.7 ± 0.2a | 0.8 ± 0.2a |
Bicarbonate (mmol/L) | 27.8 ± 0.5 | 27.6 ± 1.7 | 26.8 ± 1.1 | 26.7 ± 2.4 |
Pi (mg/dL) | 7.5 ± 0.5 | 7.6 ± 0.3 | 9.8 ± 0.4a | 8.2 ± 0.5c |
PTH (pg/mL) | 108.4 ± 9.4 | 118.6 ± 18.4 | 364.1 ± 21.4a | 227.3 ± 17.5a,c |
25(OH)D3 (ng/mL) | 113.2 ± 12.3 | 103.7 ± 23.4 | 43.5 ± 15.4b | 117.8 ± 15.3c |
1,25(OH)2D3 (pg/mL) | 298.4 ± 23.4 | 278.4 ± 26.9 | 105.6 ± 24.8b | 302.4 ± 37.8c |
BUN, blood urea nitrogen; PTH, parathyroid hormone; WT, wild‐type.
Twelve‐month‐old, male, WT, and Ctns−/− mice were treated with 25(OH)D3 and 1,25(OH)2D3 (75 μg/kg/day and 60 ng/kg/day, respectively) or ethylene glycol as vehicle for 6 weeks. Four groups of mice were included: WT + vehicle, WT + 25(OH)D3 + 1,25(OH)2D3, Ctns−/− + vehicle, and Ctns−/− + 25(OH)D3 + 1,25(OH)2D3. Ctns−/− + vehicle mice were fed ad libitum, while other groups of mice were fed the same food intake as that of Ctns−/− + vehicle mice. Data are expressed as mean ± standard error of the mean.
P < 0.05, significantly higher in Ctns−/− + vehicle and Ctns−/− + 25(OH)D3 + 1,25(OH)2D3 mice vs. WT + vehicle and WT + 25(OH)D3 + 1,25(OH)2D3 mice, respectively.
P < 0.05, significantly lower in Ctns−/− + vehicle and Ctns−/− + 25(OH)D3 + 1,25(OH)2D3 mice vs. WT + vehicle and WT + 25(OH)D3 + 1,25(OH)2D3 mice, respectively.
P < 0.05, significantly different between Ctns−/− + vehicle vs. Ctns−/− + 25(OH)D3 + 1,25(OH)2D3 mice.