Related Experiment Videos
Tetrachloroethane, pentachloroethane, and hexachloroethane: genetic and biochemical studies
G Bronzetti1, E Morichetti, R Del Carratore
1Istituto di Mutagenesi e Differenziamento, CNR, Pisa, Italy.
Teratogenesis, Carcinogenesis, and Mutagenesis
|January 1, 1989
Summary
Tetrachloroethane, pentachloroethane, and hexachloroethane showed genotoxicity in yeast. These halogenated hydrocarbons also caused significant toxicity in mice, decreasing cytochrome P450 levels and enzyme activities.
Area of Science:
- Toxicology
- Genetics
- Biochemistry
Background:
- Halogenated hydrocarbons are environmental contaminants.
- Assessing their genotoxic and toxic effects is crucial for risk assessment.
Purpose of the Study:
- To evaluate the genotoxicity of tetrachloroethane (TTCE), pentachloroethane (PCE), and hexachloroethane (HCE) in yeast.
- To investigate the in vivo toxic effects of these compounds on mouse liver enzymes.
Main Methods:
- Yeast Saccharomyces cerevisiae (strain D7) was used in suspension tests with and without metabolic activation (S9).
- Mitotic gene conversion and point reverse mutation assays were performed.
- In vivo toxicity was assessed by measuring cytochrome P450 (cyt. P450) content and the activities of pentoxyresorufin O-dealkylase (PROD) and ethoxy-resorufin O-deethylase (EROD) in mouse hepatic microsomes.
Main Results:
- TTCE, PCE, and HCE induced genotoxicity in yeast cells from the logarithmic growth phase.
- PCE also caused significant gene conversion and mutation in stationary phase cells with S9 activation.
- Acute intoxication in mice led to marked decreases in cyt. P450, EROD, and PROD activities, with TTCE and PCE showing preferential effects on P448 forms.
Conclusions:
- TTCE, PCE, and HCE exhibit genotoxic potential.
- These compounds induce significant toxicity in vivo, impacting key drug-metabolizing enzyme systems.
- The results highlight the need for further investigation into the specific mechanisms of toxicity for these halogenated hydrocarbons.