Abstract
It is now well documented that in most instances, the production and accumulation of reactive intermediates in a living organism depend upon the relative activity of several enzymes (for review, see 1,2,3). Qualitative or quantitative modifications of these enzymatic activities might thus lead either to an enhancement or a decrease in the toxicity of a given chemical. Precise knowledge of the biochemical mechanisms which control these enzymatic systems could be of paramount importance if one wants to predict or modify the biological potential of cells to produce active metabolites.
Keywords
- Fetal Liver Cell
- Aryl Hydrocarbon Hydroxylase
- Cytochrome P450 Content
- Epoxide Hydrolase Activity
- Testosterone Estradiol
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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Gielen, J.E., De Graeve, J., Goujon, F., Kremers, P., Van Cantfort, J. (1982). Monooxygenase and Epoxide Hydrolase Regulation in Primary Fetal Rat Liver Cell Culture. In: Snyder, R., et al. Biological Reactive Intermediates—II. Advances in Experimental Medicine and Biology, vol 136. Springer, New York, NY. https://doi.org/10.1007/978-1-4757-0674-1_6
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DOI: https://doi.org/10.1007/978-1-4757-0674-1_6
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