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Role of cytochrome P450 (CYP) metabolites of arachidonic acid in the regulation of cAMP in HEK293 cells Open Access

Descriptions

Other title
Subject/Keyword
Epoxyeicosatrienoic acids (EETs)
Dihydroxyeicosatrienoic acids (DHETs)
Cyclic AMP
Forskolin
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Abukhashim, Mohamed
Supervisor and department
Seubert, John (Faculty of Pharmacy and Pharmaceutical Sciences)
El-Kadi, Ayman (Faculty of Pharmacy and Pharmaceutical Sciences)
Examining committee member and department
Clanachan, Alexander (Department of Pharmacology, Faculty of Medicine and Dentistry)
Department
Faculty of Pharmacy and Pharmaceutical Sciences
Specialization

Date accepted
2011-09-30T15:52:03Z
Graduation date
2011-11
Degree
Master of Science
Degree level
Master's
Abstract
Cytochrome P450 epoxygenases metabolize arachidonic acid to epoxyeicosatrienoic acids (EETs), which in turn are converted to dihydroxyeicosatrienoic acids (DHETs) by soluble epoxide hydrolase (sEH). EETs are known to modulate a number of vascular and renal functions but the exact signaling mechanism(s) of these EET-mediated effects remains unknown. Purpose: To investigate the role of EETs and DHETs in regulating cAMP production via adenylyl cyclase (AC) in a human embryonic kidney cell line (HEK 293). Method: HEK 293 cells were treated with vehicle, forskolin, epinephrine, 11,12-EET, 11,12-DHET, as well as potential pathway and G-protein inhibitors to assess changes in cAMP production. Results: Co-administering 11,12-EET with forskolin or epinephrine effectively eliminated the increased cAMP levels observed in cells treated with forskolin alone. The inhibitory effect of EETs on forskolin-mediated cAMP production was abolished when cells were treated with a sEH inhibitor (tAUCB). 11,12-DHET also negated the effects of forskolin, suggesting the inhibitory effect observed in EET-treated cells could be attributed to the downstream metabolites, DHETs. In contrast, inhibition of phosphodiesterase IV (PDE4) with rolipram eliminated the effects of EETs or DHETs, and Gαi with pertussis toxin also resulted in enhanced cAMP production. Conclusion: Our data suggest that DHETs regulate cAMP production via PDE4 and Gαi protein. Moreover, they provide novel evidence as to how EET-mediated signaling may alter G-protein coupling in HEK 293 cells
Language
English
Rights
Permission is hereby granted to the University of Alberta Libraries to reproduce single copies of this thesis and to lend or sell such copies for private, scholarly or scientific research purposes only. Where the thesis is converted to, or otherwise made available in digital form, the University of Alberta will advise potential users of the thesis of these terms. The author reserves all other publication and other rights in association with the copyright in the thesis and, except as herein before provided, neither the thesis nor any substantial portion thereof may be printed or otherwise reproduced in any material form whatsoever without the author's prior written permission.
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