INFLUENCE OF DIURESIS ON ENZYMURIA

Urinary excretion of renal brush border enzymes may serve as an early marker of renal injury. However, the distinction between physiological and pathological levels remains controversial, since enzymuria is affected by physiological parameters. To clarify the influence of diuresis, we investigated t...

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Veröffentlicht in:Renal failure 2001-01, Vol.23 (3-4), p.377-384
Hauptverfasser: Frey, Katrin, Mondorf, Werner A., Geiger, Helmut, Mondorf, Ulrich F.
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Sprache:eng
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Zusammenfassung:Urinary excretion of renal brush border enzymes may serve as an early marker of renal injury. However, the distinction between physiological and pathological levels remains controversial, since enzymuria is affected by physiological parameters. To clarify the influence of diuresis, we investigated the urinary excretion of alanine-aminopeptidase (AAP; EC 3.4.11.2) as function of diuretic state. 17 healthy volunteers of both sexes were subjected to protocols with sudden or prolonged water load preceded and followed by a thirst period. Urinary excretion of AAP was measured using an enzyme kinetic assay. As expected AAP excretion increased with urine flow, the increments diminished yielding an overall excretion pattern that resembled saturation kinetics. This function is described by a mathematical model. This model assumes, that AAP is released in proximal tubules at a constant rate and reabsorbed or inactivated in the distal tubule and collecting duct. Non-linear fits of the model equation to our data allowed two parameters, χ and μ, to be defined. χ describes the rate of AAP release independent of urinary flow, and μ the ratio of distal tubular reabsorption or inactivation. If a substrate is not reabsorbed at all, μ approximates zero. Since μ fitted for AAP differed significantly from zero, this indicates reabsorption or inactivation of AAP in the distal nephron. Therefore, our study supports the theory of flow-dependent reabsorption or inactivation of AAP in the distal nephron.
ISSN:0886-022X
1525-6049
DOI:10.1081/JDI-100104721