Table 3.
Everolimus |
2-Cyanoethyl Alsterpaullone |
|||
---|---|---|---|---|
E− (n = 8) | E+ (n = 6) | A− (n = 11) | A+ (n = 9) | |
Body weight, g | 226.1 ± 5.3 | 171.9 ± 4.5‡ | 242.5 ± 3.6 | 222.7 ± 8.8* |
Kidney weight/body weight, % | 0.26 ± 0.01 | 0.22 ± 0.01† | 0.24 ± 0.01 | 0.24 ± 0.01 |
Urine volume, ml/day | 15.4 ± 1.8 | 17.7 ± 3.9 | 25.3 ± 2.0 | 29.1 ± 2.3 |
BUN, mg/dl | 41.9 ± 4.8 | 68.1 ± 5.0† | 39.2 ± 2.0 | 54.2 ± 7.2* |
PCr, mg/dl | 0.90 ± 0.07 | 1.17 ± 0.08† | 1.07 ± 0.05 | 1.22 ± 0.01 |
CCr, ml·min−1·kg−1 | 2.83 ± 0.17 | 1.41 ± 0.16‡ | 2.69 ± 0.19 | 2.44 ± 0.27 |
Albumin excretion, mg/day | 8.4 ± 4.5 | 2.4 ± 1.0 | 5.7 ± 1.5 | 11.8 ± 3.9 |
Data represent means ± SE for n rats. E− and A−, Nx rats administered vehicle; E+ and A+, Nx rats daily administered everolimus (2 mg/kg) and 2-cyanoethyl alsterpaullone (0.5 mg/kg) for 14 days, respectively.
P < 0.05,
P < 0.01,
P < 0.001, significantly different from vehicle-treated rats.