Abstract | BACKGROUND: Flow-mediated dilation (FMD) of human conduit arteries is, in part, related to shear stress-induced release of endothelium-derived nitric oxide (NO). However, NO synthase inhibitors do not completely abolish this FMD-response. Recently, a cytochrome P450 (CYP) epoxygenase of the 2C family was linked to NO- and prostacyclin-independent relaxation of conduit arteries. We therefore evaluated the contribution of CYP 2C9 to FMD in humans. METHODS AND RESULTS: FMD of the radial artery was determined in 12 healthy volunteers by high-resolution ultrasound and analyzed before and after intra-arterial infusion of sulfaphenazole, a specific CYP 2C9 inhibitor, L-NMMA ( NO synthase inhibitor) and co-infusion of both. Endothelium-independent vasodilation was characterized after intra-arterial infusion of SNP. FMD was reduced after sulfaphenazole (11.5+/-0.87% vs. 7.4+/-0.95%, p<0.01), after L-NMMA (6.0+/-0.71%; p<0.01), and after co-infusion 3.9+/-0.73% (p<0.05 vs. L-NMMA; p<0.01 vs. sulfaphenazole). Sulfaphenazole had no effect on endothelium-independent vasodilation. In patients with chronic heart failure, the portion of FMD blocked by sulfaphenazole was not affected. CYP 2C was detected by immunohistochemistry in radial artery samples obtained from patients undergoing coronary bypass surgery. CONCLUSIONS: FMD in human conductance arteries is reduced after inhibition of CYP 2C9, supporting the concept that CYP 2C metabolites contribute to endothelium-mediated vasodilation of peripheral conduit arteries in vivo. In patients with heart failure, the CYP-dependent FMD appears to be preserved.
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Authors | Dieter Fischer, Ulf Landmesser, Stephan Spiekermann, Denise Hilfiker-Kleiner, Marian Hospely, Maja Müller, Rudi Busse, Ingrid Fleming, Helmut Drexler |
Journal | European journal of heart failure
(Eur J Heart Fail)
Vol. 9
Issue 8
Pg. 770-5
(Aug 2007)
ISSN: 1388-9842 [Print] England |
PMID | 17572144
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Infective Agents
- Sulfaphenazole
- CYP2C9 protein, human
- Cytochrome P-450 CYP2C9
- Aryl Hydrocarbon Hydroxylases
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Topics |
- Aged
- Anti-Infective Agents
(pharmacology)
- Arteries
(physiology)
- Aryl Hydrocarbon Hydroxylases
(physiology)
- Chronic Disease
- Cytochrome P-450 CYP2C9
- Female
- Heart Failure
(physiopathology)
- Hemorheology
- Humans
- Immunohistochemistry
- Male
- Regional Blood Flow
(physiology)
- Sulfaphenazole
(pharmacology)
- Vasodilation
(drug effects, physiology)
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