HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The metabolism and testicular toxicity of cyclohexylamine in rats and mice during chronic dietary administration.

Abstract
Cyclohexylamine hydrochloride has been given in the diet to mice and to Wistar and DA rats for 13 weeks, to provide a constant intake of 400 mg of the base/kg/day. Significantly decreased food intake and body weight gain were found in both strains of rats but not mice. The metabolism of [14C]cyclohexylamine was widely different in Wistar and DA rats and in rats and mice, and these differences were not altered appreciably by chronic intake for 13 weeks. The differences in metabolism resulted in marked and persistent differences in the concentrations of the hydroxylated metabolites in the plasma and testes of treated animals with Wistar much greater than DA much greater than mice. After 7 and 13 weeks testicular atrophy was demonstrated in both strains of rats given cyclohexylamine diet by a decrease in organ weight and by histological changes. DA rats appeared more sensitive to testicular toxicity from cyclohexylamine than Wistar rats, while mice showed no evidence of testicular damage. These data show that the development of testicular toxicity is not related to the extent of hydroxylation. The concentrations of cyclohexylamine in the plasma and testes of the treated animals were lower in mice than in either strain of rats despite a similar daily intake. This suggests that species differences in pharmacokinetics may contribute to the apparent difference in sensitivity to testicular toxicity.
AuthorsA Roberts, A G Renwick, G Ford, D M Creasy, I Gaunt
JournalToxicology and applied pharmacology (Toxicol Appl Pharmacol) Vol. 98 Issue 2 Pg. 216-29 (Apr 1989) ISSN: 0041-008X [Print] United States
PMID2711388 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cyclohexylamines
Topics
  • Animals
  • Cyclohexylamines (metabolism, toxicity)
  • Diet
  • Drinking (drug effects)
  • Eating (drug effects)
  • Hydroxylation
  • Male
  • Mice
  • Organ Size (drug effects)
  • Rats
  • Rats, Inbred Strains
  • Species Specificity
  • Testis (drug effects, pathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: