STUDIES ON THE EFFECTS OF L(ALPHA-S,5S)-ALPHA- AMINO-3-CHLORO-4,5-DIHYDRO-5-ISOXAZOLEACETIC ACID (AT-125) ON 4-AMINOPHENOL-INDUCED NEPHROTOXICITY IN THE FISCHER-344 RAT
Ml. Anthony et al., STUDIES ON THE EFFECTS OF L(ALPHA-S,5S)-ALPHA- AMINO-3-CHLORO-4,5-DIHYDRO-5-ISOXAZOLEACETIC ACID (AT-125) ON 4-AMINOPHENOL-INDUCED NEPHROTOXICITY IN THE FISCHER-344 RAT, Archives of toxicology, 67(10), 1993, pp. 696-705
4-Aminophenol (para-aminophenol; PAP) causes selective necrosis to the
S-3 segment of the proximal tubule in experimental animals. The mecha
nism of PAP nephrotoxicity has not been fully elucidated, although it
has been suggested to involve glutathione (GSH)-dependent S-conjugatio
n followed by processing by the enzyme gamma-glutamyl transpeptidase (
IFT) to the corresponding cysteine S-conjugate. This proposed toxicity
mechanism was probed further by administering L-(alpha alpha-amino-3-
chloro-4,5-dihydro-5-isoxazoleacetic acid (AT-125), a potent gamma GT
inhibitor, to Fischer 344 (F344) rats before treatment with PAP (100 m
g/kg). AT-125 pretreatment did not appear to protect against PAP-induc
ed nephrotoxicity as assessed by renal histopathology, clinical chemis
try and proton nuclear magnetic resonance (H-1 NMR) spectroscopy of ur
ine. These data suggest that renal gamma GT activity is not a prerequi
site for PAP nephrotoxicity and that the generation of a cysteine S-co
njugate is not a unique requirement for the induction of PAP nephrotox
icity.