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. 2010 Jan 13;298(4):F923–F934. doi: 10.1152/ajprenal.00567.2009

Table 3.

Effects of administration of everolimus and Cdc2 inhibitor on renal function in Nx rats

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.