Abstract

Administration of carbon tetrachloride (CCl 4) to rats led to an increase in expired ethane by 15 min. Prior treatment of rats with phenobarbital led to a significant increase in both CCl 4-stimulated ethane expiration and hepatic microsomal lipid diene conjugation, while prior treatment with 3-methylcholanthrene or CCl 4 led to a decrease in both parameters. Treatment with isopropanol increased CQ 4-stimulated ethane expiration, while neither ethanol nor diethyl maleate treatment altered the response to CCl 4. Cobaltous chloride treatment significantly decreased CCl 4-stimulated ethane expiration. A strong correlation was found between CCl 4-stimulated hepatic microsomal lipid diene conjugation and ethane expiration.

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