Examination of the structure-toxicity relationships of l-cysteine-S-conjugates of halogenated alkenes and their corresponding mercapturic acids in rat renal tissue slices

G. J. Stijntjes, J. N.M. Commandeur, J. M. te Koppele, S. McGuinness, A. J. Gandolfi, N. P.E. Vermeulen

Research output: Contribution to journalArticle

14 Scopus citations

Abstract

Rat kidney slices were produced using a modified version of a mechanical tissue slicer. The slices were incubated with various concentrations of l-cysteine conjugates and mercapturic acids of halogenated alkenes in a submersion incubation system. The slices showed a time- and concentration-dependent toxicity to the nephrotoxic conjugates. The five l-cysteine conjugates tested: S-(1,2-dichlorovinyl)-l-cysteine (1,2-DCVC), S-(1,1,2,2-tetrafluoroethyl)-l-cysteine (TFEC), S-(1-chloro-1,2,2-trifluoroethyl)-l-cysteine (CTFEC), S-(1,1-dichloro-2,2-difluoroethyl)-l-cysteine (DCDFEC) and S-(1,1, dibromo-2,2-difluoroethyl)-l-cysteine (DBDFEC) were more toxic compared to the corresponding mercapturic acids. Comparing the in vitro toxicity data with the in vivo data for the same compounds results in similar ranking for the relative nephrotoxicity of the conjugates.

Original languageEnglish (US)
Pages (from-to)67-79
Number of pages13
JournalToxicology
Volume79
Issue number1
DOIs
StatePublished - Mar 30 1993

    Fingerprint

Keywords

  • Halogenated alkenes
  • Mercapturic acids
  • Nephrotoxicity
  • Rat renal slice
  • l-cysteine conjugates

ASJC Scopus subject areas

  • Toxicology

Cite this