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Hyesook Kim, Ph.D. |
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Wayne State University
Adjunct Professor,
Institute of Environmental Health Sciences |
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Tel. |
(313) 961-1606 |
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Fax. |
(313) 577- 0082
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Email: |
hskim@aol.com |
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Address: |
Institute of
Environmental Health Sciences
Wayne State University
2727 Second Avenue, Room 4000
Detroit, MI 48201-2654 |
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Research Interests: |
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Cytochrome P450 (CYP)
2C11, CYP2C23, CYP2B1, and CYP2B2 expressed in rats, CYP2C1
and CYP2C2 expressed in rabbits, and CYP2C8 and CYP2C9/2C10
expressed in human have been identified to be arachidonic
acid (AA) epoxygenases. Recently, CYP2J, a novel CYP
subfamily with AA epoxygenase activity, has been found in
humans (CYP2J2), rats (CYP2J3) and rabbits (CYP2J1).
Sprague-Dawley rats were treated with dexamethasone (DEX).
DEX treatment dramatically decreased hepatic AA epoxygenase
activity. DEX treatment decreased CYP2C23 levels but failed
to affect CYP2B1, CYP2B2 or CYP2C11 levels. The results
suggest that the decrease in AA epoxygenase activity after
DEX treatment was a result of decreased CYP2C23 levels. Our
laboratory will study effect of DEX on renal AA epoxygenases
and soluble epoxide hydrolase. |
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Select Publications: |
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A. S. A. Gracon, S. J. Pernecky, M. C. Milletti, J.-A Park,
Y. Yuan and H. Kim (2005) Computational characterization of
a series of eicosanoids. Letters in Drug Design &
Discovery 2,239-244.
H. Kim, D. A. Putt, R. C. Zangar, C. R. Wolf, F. P. Guengerich, R. J.
Edwards, P. F. Hollenberg and R. F. Novak (2001)
Differential induction of rat hepatic cytochromes P450 3A,
2B and 2E1 in response to pyridine treatment. Drug Metab.
Dispos., 29, 353-360.
Patent: "Detection of hypertension using immunoreactive
metabolic products" US patent #6,440,682 and #6,534,282 (2
divisional patents issued on 8/27/02 & 3/18/2003,
respectively),
http://patft.uspto.gov/netahtml/srchnum.htm |
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