Intrarenal Dynamics in the Pathogenesis and Prevention of Acute Urate Nephropathy

and pH were selectively altered to determine the relative protective roles of these factors in a rat model of acute urate nephropathy. Various prehyper-uricemic conditions were established in five groups of animals: (a) normopenic Wistar rats given no pre-treatment (Group I); (b) Wistar rats given acetazola-mide, 20 mg/kg, and isotonic NaHCO3 to produce urine alkalinization (Group II); (c) Wistar rats in which a moderate diuresis, similar to that observed in Group II but without urine alkalinization, was induced with furosemide, 2 mg/kg (Group III); (d) Wistar rats in which a high-flow solute diuresis was induced with furosemide, 15 mg/kg (Group IV); (e) Brattleboro rats, homozygous for pituitary diabetes insipidus, that had a spontaneous high-flow water diuresis (Group V). A comparable level of hyper-uricemia (19.4+2.2 mg/100 ml) was achieved in all animals with intravenous urate infusion. Clearance and micropuncture studies were performed before and 1 h after induction of hyperuricemia. Group I rats had mean falls in renal plasma flow and glomerular filtration rate of 83 and 86%, respectively; nephron filtration rate decreased 66%, and tubular and micro-vascular pressures increased twofold. In Group II there were 45 and 47 % declines in renal plasma flow and glomerular filtration rate, respectively, a 66% fall in nephron filtration rate, and a 30 % increase in tubular and vascular pressures. Moderate amounts of urate were seen in the kidneys. Group III had changes in renal function identical to Group II sug-gesting that the moderate prehyperuricemic diuresis in the latter group and not urine alkalinization pro-duced the partial protection observed. Groups IV Portions of this study appeared in abstract form in th