Cited by 177Nitric Oxide and Endothelin EffectsMitochondrial Function and PathologyEicosanoids and Hypertension Pharmacology

Oxidative Stress and Mitochondrial Aldehyde Dehydrogenase Activity: A Comparison of Pentaerythritol Tetranitrate with Other Organic Nitrates

Daiber, Andreas, Oelze, Matthias, Coldewey, Meike, Bachschmid, Markus, Wenzel, Philip, Sydow, Karsten, Wendt, Maria, Kleschyov, Andrei L +4 more·2004·Molecular Pharmacology

Abstract

Mitochondrial aldehyde dehydrogenase (ALDH-2) was recently identified to be essential for the bioactivation of glyceryl trinitrate (GTN). Here we assessed whether other organic nitrates are bioactivated by a similar mechanism. The ALDH-2 inhibitor benomyl reduced the vasodilator potency, but not the efficacy, of GTN, pentaerythritol tetranitrate (PETN), and pentaerythritol trinitrate in phenylephrine-constricted rat aorta, whereas vasodilator responses to isosorbide dinitrate, isosorbide-5-mononitrate, pentaerythritol dinitrate, pentaerythritol mononitrate, and the endothelium-dependent vasodilator acetylcholine were not affected. Likewise, benomyl decreased GTN- and PETN-elicited phosphorylation of the cGMP-activated protein kinase substrate vasodilator-stimulated phosphoprotein (VASP) but not that elicited by other nitrates. The vasodilator potency of organic nitrates correlated with their potency to inhibit ALDH-2 dehydrogenase activity in mitochondria from rat heart and increase mitochondrial superoxide formation, as detected by chemiluminescence. In contrast, mitochondrial ALDH-2 esterase activity was not affected by PETN and its metabolites, whereas it was inhibited by benomyl, GTN applied in vitro and in vivo, and some sulfhydryl oxidants. The bioactivation-related metabolism of GTN to glyceryl-1,2-dinitrate by isolated RAW macrophages was reduced by the ALDH-2 inhibitors benomyl and daidzin, as well as by GTN at concentrations >1 microM. We conclude that mitochondrial ALDH-2, specifically its esterase activity, is required for the bioactivation of the organic nitrates with high vasodilator potency, such as GTN and PETN, but not for the less potent nitrates. It is interesting that ALDH-2 esterase activity was inhibited by GTN only, not by the other nitrates tested. This difference might explain why GTN elicits mitochondrial superoxide formation and nitrate tolerance with the highest potency.

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References 44 · Cited by 177

Authors
Daiber, A., Oelze, M., Coldewey, M., Bachschmid, M., Wenzel, P., Sydow, K., Wendt, M., Kleschyov, A. L., Stalleicken, D., Ullrich, V., Mülsch, A., & Münzel, T.
Affiliations
University Medical Center Hamburg-Eppendorf (DE)
Venue
Molecular Pharmacology
Publisher
Elsevier BV
Published
2004-12
Volume
66
Issue
6
Pages
1372-1382
ISSN
0026-895X (ISSN-L)
OpenAlex
W2115871167
Cited by
177
References
44
Citations by year
2025: 3 · 2024: 3 · 2023: 3 · 2022: 4 · 2021: 5 · 2020: 4 · 2019: 6 · 2018: 7 · 2017: 12 · 2016: 7 · 2015: 10 · 2014: 5 · 2013: 10 · 2012: 10
FWCI
7.21
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Pharmacology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Eicosanoids and Hypertension Pharmacology
Keywords
mitochondrial aldehyde dehydrogenase 2, organic nitrates, PETN, nitroglycerin, metabolic activation, benomyl, oxidative stress, VASP phosphorylation, nitrate tolerance, daidzin, RAW 264.7 macrophages
MeSH terms
Ethanol, Aldehyde Dehydrogenase, Animals, Aorta, Benomyl, Endothelium, Vascular, Esterases, Nitroglycerin, Isometric Contraction, Mitochondria, Heart, Muscle, Smooth, Vascular, Pentaerythritol Tetranitrate, Vasodilator Agents, Rats, Wistar, Reactive Oxygen Species, Oxidative Stress, Models, Animal, Rats, In Vitro Techniques

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