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Tumorigenicity of nickel subsulfide in Strain A/J mice.

Abstract
The pulmonary tumor response of Strain A mice has been reported to be a rapid and efficient predictor of carcinogenic potential for a variety of chemicals. The route of exposure has usually been by intraperitoneal injection (i.p.) of solubilized materials. We compared intratracheal (i.t.) instillation as a more representative route typical of human exposures, with i.p. injection of nickel subsulfide, a potent animal carcinogen. Animals were sacrificed either 20 weeks after the first dosing, or were held until 45 weeks after the first dosing. Urethane, a positive control, produced a significant increase in pulmonary tumor response after i.t. instillation as well as i.p. injection. For nickel subsulfide treated animals, there was no evidence of a dose-related increase in pulmonary tumor response in any i.p. or i.t. treatment group when compared with age-matched controls.
AuthorsD A McNeill, C E Chrisp, G L Fisher
JournalDrug and chemical toxicology (Drug Chem Toxicol) Vol. 13 Issue 1 Pg. 71-86 ( 1990) ISSN: 0148-0545 [Print] United States
PMID2379474 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Carcinogens
  • Urethane
  • Nickel
  • nickel subsulfide
Topics
  • Adenoma (chemically induced, pathology)
  • Administration, Inhalation
  • Animals
  • Carcinogens
  • Injections, Intraperitoneal
  • Lung Neoplasms (chemically induced, pathology)
  • Male
  • Mice
  • Mice, Inbred A
  • Nickel (toxicity)
  • Particle Size
  • Urethane (toxicity)

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