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Induction of light hydrocarbon nephropathy by p-dichlorobenzene.

Abstract
In order to clarify the etiology of a dose-related increase in the incidence of tubular cell adenocarcinomas of the kidney in male rats, the nephrotoxicity of p-dichlorobenzene (p-DCB) was investigated in a subchronic study. Groups of ten male and ten female Fischer 344 rats were dosed by gavage with 0 (controls), 75, 150, 300 or 600 mg p-DCB/kg/day in corn oil. Half of the animals were sacrificed after 4 weeks and the remainder after 13 weeks. Increased urinary LDH and epithelial cell excretion and exacerbation of hyaline droplet accumulation in the cytoplasm of renal cortical cells were observed in male rats over the entire dose range investigated. Tubular single cell necrosis, dilated tubules with granular cast formation in the outer zone of the medulla, were evident in male rats after 4 and 13 weeks of treatment with doses of 150-600 mg/kg/day. In female rats there was no indication of a nephrotoxic action of p-DCB. The effects on the kidney, both in their morphological characteristics and the fact that they occur exclusively in male animals, correspond to the light hydrocarbon nephropathy observed as a result of short-term treatment with a number of aliphatic and cyclic hydrocarbons. The development of cortical renal tumors seems to be associated with this kind of kidney damage which is unique to male rats. The literature on this subject generally regards these renal effects as not predictive for man.
AuthorsE Bomhard, G Luckhaus, W H Voigt, E Loeser
JournalArchives of toxicology (Arch Toxicol) Vol. 61 Issue 6 Pg. 433-9 ( 1988) ISSN: 0340-5761 [Print] Germany
PMID2903729 (Publication Type: Journal Article)
Chemical References
  • Chlorobenzenes
  • 4-dichlorobenzene
  • L-Lactate Dehydrogenase
  • Acetylglucosaminidase
  • Aminopeptidases
  • CD13 Antigens
Topics
  • Acetylglucosaminidase (urine)
  • Adenocarcinoma (chemically induced, pathology, ultrastructure)
  • Aminopeptidases (urine)
  • Animals
  • CD13 Antigens
  • Chlorobenzenes (toxicity)
  • Female
  • Kidney Neoplasms (chemically induced, pathology, ultrastructure)
  • L-Lactate Dehydrogenase (urine)
  • Male
  • Microscopy, Electron
  • Organ Size (drug effects)
  • Rats
  • Rats, Inbred F344
  • Sex Factors

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