Objectives. Patients with renal mass reduction of more than 50% are at
increased risk for progressive renal failure. Lipid-lowering agents h
ave been shown to preserve renal function in various models of chronic
renal failure. This study was performed to evaluate the hemodynamic e
ffects of lovastatin, a 3-hydroxy-3-meth-ylglutaryl-coenzyme A reducta
se inhibitor, in the remnant kidney model. Methods. Two groups of anim
als were studied. Group 1 (n = 9) served as controls and group 2 (n =
14) received lovastatin, 15 mg/kg/day orally, for 2 weeks after renal
ablation. Glomerular filtration rate (GFR, inulin clearance), renal bl
ood flow (RBF, ultrasonic flow probe), and 24-hour protein excretion w
ere measured in anesthetized rats. Results. Two weeks after renal abla
tion, GFR was 0.28 +/- 0.09 mL/min/gkw (gram kidney weight) in group 1
, whereas in group 2, lovastatin preserved GFR at 0.58 +/- 0.3 mL/min/
gkw (P < 0.05). RBF in group 1 was 1.2 +/- 0.2 mL/min/gkw and increase
d to 2.1 +/- 0.4 mL/min/gkw in group 2 (P <0.05), representing a 43% i
ncrease. Protein excretion decreased significantly to 13 +/- 1.7 mg/24
hr in group 2. The lovastatin-treated group had a lower serum cholest
erol (59 +/- 3 mg/dL versus 71 +/- 2 mg/dL, P <0.05), but serum trigly
ceride levels were not different between the two groups. Conclusions.
Lovastatin preserves renal function in a renal ablation model after 2
weeks of treatment. It specifically increased total RBF. Therefore, in
addition to its known cholesterol lowering effect, lovastatin also ha
s the direct renal hemodynamic effect of increasing RBF and maintainin
g GFR. Copyright 1996 by Elsevier Science Inc.