Publication | Open Access
Time Course of Induction of Cytochrome P-450, NADPH-Cytochrome <i>c</i> Reductase, and Cinnamic Acid Hydroxylase by Phenobarbital, Ethanol, Herbicides, and Manganese in Higher Plant Microsomes
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Citations
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References
1980
Year
Lipid PeroxidationMetabolomic ProfilingSecondary MetabolitePlant BiochemistryHerbicides Chloro-ipcRedox BiologyOxidative StressBiosynthesisToxicologyCytochrome BMixed FunctionBiochemistryCytochrome P-450Time CourseMetabolomicsPharmacologyPrimary MetabolitePlant MetabolismBiologyNatural SciencesHigher Plant MicrosomesMetabolismMedicinePlant PhysiologyCarbonyl Metabolism
The mixed function oxidase trans-cinnamic acid 4-hydroxylase, cytochrome P-450, cytochrome b(5), and NADPH-cytochrome c (P-450) reductase were measured in microsomes from aging artichoke tuber slices exposed to manganese, ethanol, phenobarbital, and the herbicides Chloro-IPC, Dichlobenil, and Monuron. Although the microsomal hydroxylating complex is already induced by the slicing and aging process, 25 millimolar MnCl(2), 4 millimolar phenobarbital, and 300 millimolar ethanol caused a marked increase of hydroxylase activity and cytochrome P-450 content and shifted their time course. The herbicides, 200 micromolar Dichlobenil and 200 micromolar Monuron, were less effective. Chloro-IPC was slightly inhibitory. NADPH cytochrome c reductase was significantly increased only in phenobarbital-treated slices. Cytochrome b(5) was generally the least affected among the parameters being measured. The mechanisms by which these compounds increase cytochrome P-450 content and hydroxylase activity are not yet defined.
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