Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Ethylene: Genotoxic potential using the bone marrow micronucleus test following four weeks of vapor exposure

Journal Article · · Environmental and Molecular Mutagenesis
OSTI ID:88927
;  [1]
  1. Bushy Run Research Center/Union Carbide Corporation, Export, PA (United States)

Ethylene (CAS No. 74-85-1) is known to be metabolized to the mutagen ethylene oxide (EO) in mice, rats, and humans. To assess the genotoxic potential of ethylene in vivo, male Fischer 344 rats and male B6C3F1 mice (10 animals/group) were exposed to ethylene vapor for 6 hours/day, 5 days/week, and 4 weeks. Ethylene target exposure concentrations of 0, 40, 1000, and 3000 ppm were selected on the basis of pharmacokinetic studies which have shown that metabolism of ethylene to EO is saturated at ethylene exposure concentrations of approximately 1000 ppm. An EO reference group was exposed under the same conditions at a target concentration of 200 ppm. Chamber concentrations were determined approximately every 60 minutes by gas chromatography and remained within 10% of the target concentrations. Bone marrow was collected approximately 24 hours after the final exposure. Polychromatic (PCE) to normochromatic (NCE) erythrocyte ratios were determined and 2000 PCE/animal were scored for the presence of micronuclei. Ethylene did not produce statistically significant, exposure-related increases in the frequency of micronucleated PCE in either rats or mice. The frequencies of micronucleated PCE were .30, .25, .22, and .24% in rats and .22, .30, .26, and .26% in mice exposed to 0, 40, 1000, and 3000 ppm ethylene, respectively. Although the frequency of micronucleated PCE in the 40 ppm mice was statistically significant compared to the air-exposed control mice, this result was considered biologically significant since it was not reproduced at 1000 or 3000 ppm ethylene. EO produced significant increases in the frequencies of micronucleated PCE in both species when compared to the air-exposed control animals. The frequency of micronucleated PCE in EO-exposed animals was .79% in rats and .72% in mice.

OSTI ID:
88927
Report Number(s):
CONF-9405324--
Journal Information:
Environmental and Molecular Mutagenesis, Journal Name: Environmental and Molecular Mutagenesis Journal Issue: Suppl.23 Vol. 23; ISSN 0893-6692; ISSN EMMUEG
Country of Publication:
United States
Language:
English

Similar Records

Comparative cytogenetic analysis of bone marrow damage induced in male B6C3F1 mice by multiple exposures to gaseous 1,3-butadiene
Journal Article · Wed Dec 31 23:00:00 EST 1986 · Environ. Mutagen.; (United States) · OSTI ID:5844458

Effect of exposure route, regimen, and duration on benzene-induced genotoxic and cytotoxic bone marrow damage in mice
Journal Article · Sat Jul 01 00:00:00 EDT 1989 · Environmental Health Perspectives; (USA) · OSTI ID:6967902

Induction of cytogenetic damage in rodents after short-term inhalation of benzene
Journal Article · Tue Dec 31 23:00:00 EST 1985 · Environ. Mutagen.; (United States) · OSTI ID:5631909