Propylene glycol monomethyl ether (PGME): inhalation toxicity and carcinogenicity in Fischer 344 rats and B6C3F1 mice

Autor: Jerry F. Hardisty, Frank S. Cieszlak, Richard A. Corley, W.T. Stott, J. W. Crissman, Pamela J. Spencer, A.M. Schumann
Rok vydání: 2002
Předmět:
Male
Toxicology
030226 pharmacology & pharmacy
Mixed Function Oxygenases
S Phase
0403 veterinary science
Mice
0302 clinical medicine
Neoplasms
Chronic toxicity
Kidney
Inhalation
Adrenal gland
04 agricultural and veterinary sciences
Kidney Neoplasms
Dose–response relationship
medicine.anatomical_structure
Biochemistry
Liver
Enzyme Induction
Toxicity
Female
Adenoma
DNA Replication
medicine.medical_specialty
040301 veterinary sciences
Carcinogenicity Tests
Longevity
Mice
Inbred Strains

Pathology and Forensic Medicine
Nephropathy
03 medical and health sciences
Internal medicine
Administration
Inhalation

Alpha-Globulins
medicine
Animals
Molecular Biology
Carcinogen
Dose-Response Relationship
Drug

business.industry
Cell Biology
DNA
medicine.disease
Rats
Inbred F344

Rats
Endocrinology
Propylene Glycols
Carcinogens
business
Zdroj: Toxicologic pathology. 30(5)
ISSN: 0192-6233
Popis: A series of inhalation studies with propylene glycol monomethyl ether (PGME) vapor were undertaken to characterize its subchronic toxicity in mice and chronic toxicity/oncogenicity in rats and mice. Groups of male and female Fischer 344 rats and B6C3F1 mice were exposed to 0,300, 1,000, or 3,000 ppm vapor from 1 week to 2 years. Primary treatment-related effects included: initial sedation of animals exposed to 3,000 ppm and its subsequent resolution correlating with induction of hepatic mixed function oxidase activity and S-phase DNA synthesis; elevated mortality in high-exposure male rats and mice (chronic study); elevated deposition of alpha2U-globulin ( α2U-G) and associated nephropathy and S-phase DNA synthesis in male rat kidneys; accelerated atrophy of the adrenal gland X-zone infemale mice (subchronic study only); and increased occurrence and/or severity of eosinophilic foci of altered hepatocytes in male rats. No toxicologically relevant statistically significant increases in neoplasia occurred in either species. A numerical increase in the incidence of kidney adenomas occurred in intermediate-exposure male rats; however, the association with α2U-G nephropathy, a male rat specific effect, indicated a lack of relevance for human risk assessment.
Databáze: OpenAIRE