Cited by 710Nitric Oxide and Endothelin EffectsMitochondrial Function and PathologyRenin-Angiotensin System Studies

The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.

Molecular Mechanisms of Angiotensin II–Mediated Mitochondrial Dysfunction: Linking Mitochondrial Oxidative Damage and Vascular Endothelial Dysfunction

Abstract

Mitochondrial dysfunction is a prominent feature of most cardiovascular diseases. Angiotensin (Ang) II is an important stimulus for atherogenesis and hypertension; however, its effects on mitochondrial function remain unknown. We hypothesized that Ang II could induce mitochondrial oxidative damage that in turn might decrease endothelial nitric oxide (NO · ) bioavailability and promote vascular oxidative stress. The effect of Ang II on mitochondrial ROS, mitochondrial respiration, membrane potential, glutathione, and endothelial NO · was studied in isolated mitochondria and intact bovine aortic endothelial cells using electron spin resonance, dihydroethidium high-performance liquid chromatography –based assay, Amplex Red and cationic dye fluorescence. Ang II significantly increased mitochondrial H 2 O 2 production. This increase was blocked by preincubation of intact cells with apocynin (NADPH oxidase inhibitor), uric acid (scavenger of peroxynitrite), chelerythrine (protein kinase C inhibitor), N G -nitro- l -arginine methyl ester (nitric oxide synthase inhibitor), 5-hydroxydecanoate (mitochondrial ATP-sensitive potassium channels inhibitor), or glibenclamide. Depletion of p22 phox subunit of NADPH oxidase with small interfering RNA also inhibited Ang II–mediated mitochondrial ROS production. Ang II depleted mitochondrial glutathione, increased state 4 and decreased state 3 respirations, and diminished mitochondrial respiratory control ratio. These responses were attenuated by apocynin, 5-hydroxydecanoate, and glibenclamide. In addition, 5-hydroxydecanoate prevented the Ang II–induced decrease in endothelial NO · and mitochondrial membrane potential. Therefore, Ang II induces mitochondrial dysfunction via a protein kinase C–dependent pathway by activating the endothelial cell NADPH oxidase and formation of peroxynitrite. Furthermore, mitochondrial dysfunction in response to Ang II modulates endothelial NO · and generation, which in turn has ramifications for development of endothelial dysfunction.

Overview

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Crossref · 10.1161/circresaha.107.162800

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  1. 10.1161/res.88.5.529 · DOI
  2. 10.1161/res.89.12.1177 · DOI

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Metadata

Authors
Doughan, A. K., Harrison, D. G., & Dikalov, S. I.
Affiliations
United States Department of Veterans Affairs (US)
Venue
Circulation Research
Published
2008-02-29
Volume
102
Issue
4
Pages
488-496
ISSN
  • 0009-7330 (ISSN-L)
  • 1524-4571
OpenAlex
W2164444293
Cited by
710
References
43
Citations by year
2026: 24 · 2025: 24 · 2024: 19 · 2023: 32 · 2022: 33 · 2021: 44 · 2020: 39 · 2019: 31 · 2018: 31 · 2017: 36 · 2016: 54 · 2015: 29 · 2014: 58 · 2013: 51 · 2012: 50
FWCI
25.60
Type
journal article
Language
en
Open access
closed
Locations
  • Circulation Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • American Heart Association
  • National Institutes of Health (5p01hl075209-05)
  • National Heart, Lung, and Blood Institute (P0-1 HL-075209, R01HL094469, P01HL058000)
Topics
  • Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
Keywords
angiotensin II, mitochondrial dysfunction, endothelial nitric oxide, NADPH oxidase, peroxynitrite, protein kinase C, mitochondrial reactive oxygen species, mitochondrial glutathione, mitochondrial respiration, endothelial dysfunction, oxidative stress, atherogenesis, hypertension
MeSH terms
Angiotensin II, Animals, Aorta, Cattle, Cells, Cultured, Glutathione, Hydrogen Peroxide, Mitochondria, Nitric Oxide, Superoxides, Vascular Diseases, Vasoconstrictor Agents, Oxidative Stress, Cell Respiration, Mitochondrial Diseases, Endothelial Cells, Membrane Potential, Mitochondrial

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