Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.

Epidemiological studies suggest that Mediterranean diets rich in resveratrol are associated with reduced risk of coronary artery disease. Resveratrol was also shown to confer vasoprotection in animal models of type 2 diabetes and aging. However, the mechanisms by which resveratrol exerts its antioxi...

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Autori principali: Ungvari, Z, Bagi, Z, Feher, A, Recchia, F, Sonntag, W, Pearson, K, de Cabo, R, Csiszar, A
Natura: Journal article
Lingua:English
Pubblicazione: 2010
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author Ungvari, Z
Bagi, Z
Feher, A
Recchia, F
Sonntag, W
Pearson, K
de Cabo, R
Csiszar, A
author_facet Ungvari, Z
Bagi, Z
Feher, A
Recchia, F
Sonntag, W
Pearson, K
de Cabo, R
Csiszar, A
author_sort Ungvari, Z
collection OXFORD
description Epidemiological studies suggest that Mediterranean diets rich in resveratrol are associated with reduced risk of coronary artery disease. Resveratrol was also shown to confer vasoprotection in animal models of type 2 diabetes and aging. However, the mechanisms by which resveratrol exerts its antioxidative vasculoprotective effects are not completely understood. Using a nuclear factor-E(2)-related factor-2 (Nrf2)/antioxidant response element-driven luciferase reporter gene assay, we found that in cultured coronary arterial endothelial cells, resveratrol, in a dose-dependent manner, significantly increases transcriptional activity of Nrf2. Accordingly, resveratrol significantly upregulates the expression of the Nrf2 target genes NAD(P)H:quinone oxidoreductase 1, gamma-glutamylcysteine synthetase, and heme oxygenase-1. Resveratrol treatment also significantly attenuated high glucose (30 mM)-induced mitochondrial and cellular oxidative stress (assessed by flow cytometry using MitoSox and dihydroethidine staining). The aforementioned effects of resveratrol were significantly attenuated by the small interfering RNA downregulation of Nrf2 or the overexpression of Kelch-like erythroid cell-derived protein 1, which inactivates Nrf2. To test the effects of resveratrol in vivo, we used mice fed a high-fat diet (HFD), which exhibit increased vascular oxidative stress associated with an impaired endothelial function. In HFD-fed Nrf2(+/+) mice, resveratrol treatment attenuates oxidative stress (assessed by the Amplex red assay), improves acetylcholine-induced vasodilation, and inhibits apoptosis (assessed by measuring caspase-3 activity and DNA fragmentation) in branches of the femoral artery. In contrast, the aforementioned endothelial protective effects of resveratrol were diminished in HFD-fed Nrf2(-/-) mice. Taken together, our results indicate that resveratrol both in vitro and in vivo confers endothelial protective effects which are mediated by the activation of Nrf2.
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spelling oxford-uuid:0ceb17a5-9fe2-4fd9-b581-1c9ad39c0b782022-03-26T09:37:42ZResveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:0ceb17a5-9fe2-4fd9-b581-1c9ad39c0b78EnglishSymplectic Elements at Oxford2010Ungvari, ZBagi, ZFeher, ARecchia, FSonntag, WPearson, Kde Cabo, RCsiszar, AEpidemiological studies suggest that Mediterranean diets rich in resveratrol are associated with reduced risk of coronary artery disease. Resveratrol was also shown to confer vasoprotection in animal models of type 2 diabetes and aging. However, the mechanisms by which resveratrol exerts its antioxidative vasculoprotective effects are not completely understood. Using a nuclear factor-E(2)-related factor-2 (Nrf2)/antioxidant response element-driven luciferase reporter gene assay, we found that in cultured coronary arterial endothelial cells, resveratrol, in a dose-dependent manner, significantly increases transcriptional activity of Nrf2. Accordingly, resveratrol significantly upregulates the expression of the Nrf2 target genes NAD(P)H:quinone oxidoreductase 1, gamma-glutamylcysteine synthetase, and heme oxygenase-1. Resveratrol treatment also significantly attenuated high glucose (30 mM)-induced mitochondrial and cellular oxidative stress (assessed by flow cytometry using MitoSox and dihydroethidine staining). The aforementioned effects of resveratrol were significantly attenuated by the small interfering RNA downregulation of Nrf2 or the overexpression of Kelch-like erythroid cell-derived protein 1, which inactivates Nrf2. To test the effects of resveratrol in vivo, we used mice fed a high-fat diet (HFD), which exhibit increased vascular oxidative stress associated with an impaired endothelial function. In HFD-fed Nrf2(+/+) mice, resveratrol treatment attenuates oxidative stress (assessed by the Amplex red assay), improves acetylcholine-induced vasodilation, and inhibits apoptosis (assessed by measuring caspase-3 activity and DNA fragmentation) in branches of the femoral artery. In contrast, the aforementioned endothelial protective effects of resveratrol were diminished in HFD-fed Nrf2(-/-) mice. Taken together, our results indicate that resveratrol both in vitro and in vivo confers endothelial protective effects which are mediated by the activation of Nrf2.
spellingShingle Ungvari, Z
Bagi, Z
Feher, A
Recchia, F
Sonntag, W
Pearson, K
de Cabo, R
Csiszar, A
Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.
title Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.
title_full Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.
title_fullStr Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.
title_full_unstemmed Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.
title_short Resveratrol confers endothelial protection via activation of the antioxidant transcription factor Nrf2.
title_sort resveratrol confers endothelial protection via activation of the antioxidant transcription factor nrf2
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