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Differential Expression of Cytochrome P450 Enzymes from the CYP2C Subfamily in the Human Brain

Iris M. Booth Depaz, Francesca Toselli, Peter A. Wilce and Elizabeth M. J. Gillam
Drug Metabolism and Disposition March 2015, 43 (3) 353-357; DOI: https://doi.org/10.1124/dmd.114.061242
Iris M. Booth Depaz
Schools of Biomedical Sciences (I.M.B.D.) and Chemistry and Molecular Biosciences (F.T., P.A.W., E.M.J.G.), University of Queensland, Brisbane, Australia
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Francesca Toselli
Schools of Biomedical Sciences (I.M.B.D.) and Chemistry and Molecular Biosciences (F.T., P.A.W., E.M.J.G.), University of Queensland, Brisbane, Australia
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Peter A. Wilce
Schools of Biomedical Sciences (I.M.B.D.) and Chemistry and Molecular Biosciences (F.T., P.A.W., E.M.J.G.), University of Queensland, Brisbane, Australia
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Elizabeth M. J. Gillam
Schools of Biomedical Sciences (I.M.B.D.) and Chemistry and Molecular Biosciences (F.T., P.A.W., E.M.J.G.), University of Queensland, Brisbane, Australia
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Abstract

Cytochrome P450 enzymes from the CYP2C subfamily play a prominent role in the metabolic clearance of many drugs. CYP2C enzymes have also been implicated in the metabolism of arachidonic acid to vasoactive epoxyeicosatrienoic acids. CYP2C8, CYP2C9, and CYP2C19 are expressed in the adult liver at significant levels; however, the expression of CYP2C enzymes in extrahepatic tissues such as the brain is less well characterized. Form-specific antibodies to CYP2C9 and CYP2C19 were prepared by affinity purification of antibodies raised to unique peptides. CYP2C9 and CYP2C19 were located in microsomal fractions of all five human brain regions examined, namely the frontal cortex, hippocampus, basal ganglia, amygdala, and cerebellum. Both CYP2C9 and CYP2C19 were detected predominantly within the neuronal soma but with expression extending down axons and dendrites in certain regions. Finally, a comparison of cortex samples from alcoholics and age-matched controls suggested that CYP2C9 expression was increased in alcoholics.

Footnotes

    • Received September 19, 2014.
    • Accepted December 11, 2014.
  • ↵1 Current affiliation: Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.

  • This research was supported by the Australian National Health and Medical Research Council (NHMRC) [Project Grant 210215]. The New South Wales Tissue Resource Centre and Australian Brain Donor Program are supported by the University of Sydney, the NHMRC [Grant 401551], the Schizophrenia Research Institute, the National Institutes of Health National Institute on Alcohol Abuse and Alcoholism [R24 Grant AA12404], and the New South Wales Department of Health.

  • dx.doi.org/10.1124/dmd.114.061242.

  • ↵Embedded ImageThis article has supplemental material available at dmd.aspetjournals.org.

  • Copyright © 2015 by The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 43 (3)
Drug Metabolism and Disposition
Vol. 43, Issue 3
1 Mar 2015
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Rapid CommunicationShort Communication

CYP2C Expression in the Human Brain

Iris M. Booth Depaz, Francesca Toselli, Peter A. Wilce and Elizabeth M. J. Gillam
Drug Metabolism and Disposition March 1, 2015, 43 (3) 353-357; DOI: https://doi.org/10.1124/dmd.114.061242

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CYP2C Expression in the Human Brain

Iris M. Booth Depaz, Francesca Toselli, Peter A. Wilce and Elizabeth M. J. Gillam
Drug Metabolism and Disposition March 1, 2015, 43 (3) 353-357; DOI: https://doi.org/10.1124/dmd.114.061242
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