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Biochemical Characterisation of Para-aminophenol-induced Nephrotoxic Lesions in the F344 Rat

Overview
Journal Arch Toxicol
Specialty Toxicology
Date 1989 Jan 1
PMID 2730345
Citations 9
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Abstract

The acute biochemical effects of the nephrotoxin p-aminophenol (PAP) were studied in detail using a combination of conventional bioanalytical and 1H-NMR spectroscopic methods. Dosing PAP (25-100 mg/kg) to male F344 rats resulted in a dose-related proximal nephropathy with consequent elevations in urinary enzymes, glucose, and urine total protein as shown by conventional methodology. 1H-NMR spectroscopy at 400 MHz of urine from PAP-treated rats also revealed a characteristic glycosuria, with concomitant amino aciduria. The increased excretion of these compounds indicates functional defects in the proximal tubule and reduced solute reabsorption efficiency. In addition, 1H-NMR urinalysis and conventional enzymatic analysis showed a dose-related lactic aciduria. Other changes detected by 1H-NMR included a dose-related reduction in the excretion of citrate (confirmed by a conventional biochemical method) and an increase in the excretion of acetate. The degree of abnormalities shown by 1H-NMR urinalysis agreed well with histopathological observations and conventional biochemical indices of nephrotoxicity. 1H-NMR urinalysis therefore serves to highlight changes in the excretion of low MW urine components not routinely studied by conventional biochemical analysis.

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References
1.
Cohen R, Prout R . THE ORIGIN OF URINARY CITRATE. Clin Sci. 1964; 26:237-45. View

2.
Cottrell R, Agrelo C, Gangolli S, Grasso P . Histochemical and biochemical studies of chemically induced acute kidney damage in the rat. Food Cosmet Toxicol. 1976; 14(6):593-8. DOI: 10.1016/s0015-6264(76)80013-2. View

3.
Smith G, Griffiths L . Comparative metabolic studies of phenacetin and structurally-related compounds in the rat. Xenobiotica. 1976; 6(4):217-36. DOI: 10.3109/00498257609151632. View

4.
Tange J, Ross B, LEDINGHAM J . Effects of analgesics and related compounds on renal metabolism in rats. Clin Sci Mol Med. 1977; 53(5):485-92. DOI: 10.1042/cs0530485. View

5.
Maruhn D . Rapid colorimetric assay of beta-galactosidase and N-acetyl-beta-glucosaminidase in human urine. Clin Chim Acta. 1976; 73(3):453-61. DOI: 10.1016/0009-8981(76)90147-9. View