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Effect of enzyme induction on nephrotoxicity of halothane-related compounds.
Author(s) -
Ben A. Hitt,
Richard I. Mazze
Publication year - 1977
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.7721179
Subject(s) - methoxyflurane , halothane , enflurane , isoflurane , anesthetic , enzyme inducer , chemistry , nephrotoxicity , fluoride , pharmacology , in vivo , tabun , phenobarbital , enzyme , enzyme assay , anesthesia , biochemistry , medicine , toxicity , biology , soman , organic chemistry , inorganic chemistry , acetylcholinesterase , microbiology and biotechnology
Nephrotoxicity following administration of methoxyflurane has been shown to be directly related to anesthetic metabolism to inorganic fluoride. Enzyme induction should increase metabolic rate and the amount of inorganic fluoride that is released. In vivo studies in Fischer 344 rats show that enzyme induction with phenobarbital or phenytoin increases defluorination following methoxyflurane anesthesia but not after enflurane or isoflurane. In vitro, methoxyflurane defluorinase activity was increased far more than that of any of the other anesthetics. These data suggest that treatment with enzyme inducing drugs increases the risk of nephrotoxocity only if methoxyflurane is the anesthetic agent.

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