Abstract:
:Nitric oxide (NO) decreases cellular oxygen (O(2)) consumption by competitively inhibiting cytochrome c oxidase. Here, we show that endogenously released endothelial NO, either basal or stimulated, can modulate O(2) consumption both throughout the thickness of conductance vessels and in the microcirculation. Furthermore, we have shown that such modulation regulates O(2) distribution to the surrounding tissues. We have demonstrated these effects by measuring O(2) consumption in blood vessels in a hypoxic chamber and O(2) distribution in the microcirculation using the fluorescent oxygen-probe Ru(phen)(3)(2+). Removal of NO by physical or pharmacological means, or in eNOS(-/-) mice, abolishes this regulatory mechanism. Our results indicate that, in addition to its well-known effect on the regulation of vascular tone, endothelial NO plays a major role in facilitating the distribution of O(2), an action which is crucial for the adaptation of tissues, including the vessel wall itself, to hypoxia. It is possible that changes in the distribution of O(2) throughout the vessel wall may be implicated in the origin of vascular pathologies such as atherosclerosis.
journal_name
Circ Resjournal_title
Circulation researchauthors
Victor VM,Nuñez C,D'Ocón P,Taylor CT,Esplugues JV,Moncada Sdoi
10.1161/CIRCRESAHA.109.197228subject
Has Abstractpub_date
2009-05-22 00:00:00pages
1178-83issue
10eissn
0009-7330issn
1524-4571pii
CIRCRESAHA.109.197228journal_volume
104pub_type
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