Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.

Previously, we reported that the "antioxidant" compound "mitoQ" (mitochondrial-targeted ubiquinol/ubiquinone) actually increased superoxide production by bovine aortic endothelial (BAE) cell mitochondria incubated with complex I but not complex II substrates.To further define the...

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Main Authors: Brian D Fink, Yunxia O'Malley, Brian L Dake, Nicolette C Ross, Thomas E Prisinzano, William I Sivitz
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2621344?pdf=render
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author Brian D Fink
Yunxia O'Malley
Brian L Dake
Nicolette C Ross
Thomas E Prisinzano
William I Sivitz
author_facet Brian D Fink
Yunxia O'Malley
Brian L Dake
Nicolette C Ross
Thomas E Prisinzano
William I Sivitz
author_sort Brian D Fink
collection DOAJ
description Previously, we reported that the "antioxidant" compound "mitoQ" (mitochondrial-targeted ubiquinol/ubiquinone) actually increased superoxide production by bovine aortic endothelial (BAE) cell mitochondria incubated with complex I but not complex II substrates.To further define the site of action of the targeted coenzyme Q compound, we extended these studies to include different substrate and inhibitor conditions. In addition, we assessed the effects of mitoquinone on mitochondrial respiration, measured respiration and mitochondrial membrane potential in intact cells, and tested the intriguing hypothesis that mitoquinone might impart fuel selectivity in intact BAE cells. In mitochondria respiring on differing concentrations of complex I substrates, mitoquinone and rotenone had interactive effects on ROS consistent with redox cycling at multiple sites within complex I. Mitoquinone increased respiration in isolated mitochondria respiring on complex I but not complex II substrates. Mitoquinone also increased oxygen consumption by intact BAE cells. Moreover, when added to intact cells at 50 to 1000 nM, mitoquinone increased glucose oxidation and reduced fat oxidation, at doses that did not alter membrane potential or induce cell toxicity. Although high dose mitoquinone reduced mitochondrial membrane potential, the positively charged mitochondrial-targeted cation, decyltriphenylphosphonium (mitoquinone without the coenzyme Q moiety), decreased membrane potential more than mitoquinone, but did not alter fuel selectivity. Therefore, non-specific effects of the positive charge were not responsible and the quinone moiety is required for altered nutrient selectivity.In summary, the interactive effects of mitoquinone and rotenone are consistent with redox cycling at more than one site within complex I. In addition, mitoquinone has substrate dependent effects on mitochondrial respiration, increases repiration by intact cells, and alters fuel selectivity favoring glucose over fatty acid oxidation at the intact cell level.
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spelling doaj.art-770b3a928ff743819462d9ac36e9677c2022-12-22T03:19:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0141e425010.1371/journal.pone.0004250Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.Brian D FinkYunxia O'MalleyBrian L DakeNicolette C RossThomas E PrisinzanoWilliam I SivitzPreviously, we reported that the "antioxidant" compound "mitoQ" (mitochondrial-targeted ubiquinol/ubiquinone) actually increased superoxide production by bovine aortic endothelial (BAE) cell mitochondria incubated with complex I but not complex II substrates.To further define the site of action of the targeted coenzyme Q compound, we extended these studies to include different substrate and inhibitor conditions. In addition, we assessed the effects of mitoquinone on mitochondrial respiration, measured respiration and mitochondrial membrane potential in intact cells, and tested the intriguing hypothesis that mitoquinone might impart fuel selectivity in intact BAE cells. In mitochondria respiring on differing concentrations of complex I substrates, mitoquinone and rotenone had interactive effects on ROS consistent with redox cycling at multiple sites within complex I. Mitoquinone increased respiration in isolated mitochondria respiring on complex I but not complex II substrates. Mitoquinone also increased oxygen consumption by intact BAE cells. Moreover, when added to intact cells at 50 to 1000 nM, mitoquinone increased glucose oxidation and reduced fat oxidation, at doses that did not alter membrane potential or induce cell toxicity. Although high dose mitoquinone reduced mitochondrial membrane potential, the positively charged mitochondrial-targeted cation, decyltriphenylphosphonium (mitoquinone without the coenzyme Q moiety), decreased membrane potential more than mitoquinone, but did not alter fuel selectivity. Therefore, non-specific effects of the positive charge were not responsible and the quinone moiety is required for altered nutrient selectivity.In summary, the interactive effects of mitoquinone and rotenone are consistent with redox cycling at more than one site within complex I. In addition, mitoquinone has substrate dependent effects on mitochondrial respiration, increases repiration by intact cells, and alters fuel selectivity favoring glucose over fatty acid oxidation at the intact cell level.http://europepmc.org/articles/PMC2621344?pdf=render
spellingShingle Brian D Fink
Yunxia O'Malley
Brian L Dake
Nicolette C Ross
Thomas E Prisinzano
William I Sivitz
Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.
PLoS ONE
title Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.
title_full Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.
title_fullStr Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.
title_full_unstemmed Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.
title_short Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells.
title_sort mitochondrial targeted coenzyme q superoxide and fuel selectivity in endothelial cells
url http://europepmc.org/articles/PMC2621344?pdf=render
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AT brianldake mitochondrialtargetedcoenzymeqsuperoxideandfuelselectivityinendothelialcells
AT nicolettecross mitochondrialtargetedcoenzymeqsuperoxideandfuelselectivityinendothelialcells
AT thomaseprisinzano mitochondrialtargetedcoenzymeqsuperoxideandfuelselectivityinendothelialcells
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