Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989;63(2):97-106.
doi: 10.1007/BF00316430.

Biochemical characterisation of para-aminophenol-induced nephrotoxic lesions in the F344 rat

Affiliations

Biochemical characterisation of para-aminophenol-induced nephrotoxic lesions in the F344 rat

K P Gartland et al. Arch Toxicol. 1989.

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.

PubMed Disclaimer

References

    1. Clin Sci. 1964 Apr;26:237-45 - PubMed
    1. Food Cosmet Toxicol. 1976 Dec;14(6):593-8 - PubMed
    1. Xenobiotica. 1976 Apr;6(4):217-36 - PubMed
    1. Clin Sci Mol Med. 1977 Nov;53(5):485-92 - PubMed
    1. Clin Chim Acta. 1976 Dec;73(3):453-61 - PubMed

Publication types

LinkOut - more resources