The Arabinitol Appearance Rate in Laboratory Animals and Humans: Estimation from the Arabinitol/Creatinine Ratio and Relevance to the Diagnosis of Candidiasis

The effects of renal function on serum concentrations of the candidal metabolite arabinitol were studied by examining the accumulation and elimination of arabinitol in animals and humans. Serum concentrations of arabinitol rose sharply and in direct proportion to creatinine concentrations after neph...

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Bibliographic Details
Published inThe Journal of infectious diseases Vol. 146; no. 3; pp. 353 - 359
Main Authors Wong, Brian, Bernard, Edward M., Gold, Jonathan W. M., Fong, Danny, Armstrong, Donald
Format Journal Article
LanguageEnglish
Published The University of Chicago Press 01.09.1982
University of Chicago Press
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Summary:The effects of renal function on serum concentrations of the candidal metabolite arabinitol were studied by examining the accumulation and elimination of arabinitol in animals and humans. Serum concentrations of arabinitol rose sharply and in direct proportion to creatinine concentrations after nephrectomy in rats. The serum half-life of exogenous arabinitol was 20.8 hr in anephric rats but only 0.62 hr in shamnephrectomized control animals. The mean — sd apparent space of distribution of arabinitol was 419 ± 26 ml/kg. The fraction of exogenously administered arabinitol recovered in the urine was 0.73 ± 0.13 in uremic rats, 0.85 ± 0.28 in control rats, and 0.95 ± 0.10 in normal dogs. The arabinitollcreatinine clearance ratio was 0.99 ± 0.08 in normal dogs and 0.99 ± 0.25 in 22 critically ill patients with cancer. Thus arabinitol is eliminated by nearly quantitative urinary excretion and is cleared at virtually the same rate as creatinine. Therefore, the rate of arabinitol appearance in the body from any source equals the urinary arabinitol excretion rate and is directly proportional to the concentration ratio of arabinitol to creatinine in serum or urine.
Bibliography:istex:D0BFB7851B9326F9BD435C446176D9E8E2112AA3
This work was presented in part at the 8th Congress of the International Society for Human and Animal Mycology, held in Palmerston North, New Zealand, on February 8–12, 1982.
ark:/67375/HXZ-QVRRXN78-4
ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/146.3.353