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. Author manuscript; available in PMC: 2019 Apr 1.
Published in final edited form as: J Endocrinol. 2018 Apr;237(1):43–58. doi: 10.1530/JOE-17-0536

Table 2.

Control of hyperglycemia by leflunomide in ob/ob mice

Drug Number of mice (N) Blood glucose concentration (mg/dL) Body weight (g) Food intake (g/d) p value*


Before After p value Before After Change p value*
Vehicle 6 234±16 252±22 0.697 47.8±2.9 48.0± 3.1 0.12±0.21 4.9± 0.23
Leflunomide 7 275±12 111±6 0.001 48.4±0.48 48.5±0.51 −0.02±0.13 0.252 5.0 ±0.09 0.687
Uridine 4 210±12 253±15 0.153 48.7± 0.68 48.5 ±0.69 −0.02±0.08 0.793 4.9 ±0.07 1.000
Lef + Uridine 4 222±15 97±15 0.021 48.5±1.21 48.4±1.06 −0.3±0.04 0.385 4.8 ±0.04 0.272

ob/ob mice (male, 8–10 wks) were treated with the vehicle (1.5% CMC, daily, gavage), leflunomide (35 mg/kg, daily, gavage), uridine (2 g/kg, twice daily, i.p.) or leflunomide (35 mg/kg, daily, gavage) + uridine (2 g/kg, twice daily, i.p.) for three days. After fasting for 6 hr, blood glucose levels were measured and statistically analyzed by a paired Student t test. Body weight of mice were measured before and 3 days after treatment. Food consumption was measured on individual mouse in a separate cage on day 3 after treatment.

*

Compared to the vehicle control.