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The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.

Resveratrol induces mitochondrial biogenesis in endothelial cells

Open access
Csiszar, Anna, Labinskyy, Nazar, Pinto, John T., Ballabh, Praveen, Zhang, Hanrui, Losonczy, Gyorgy, Pearson, Kevin, de Cabo, Rafael, Pacher, Pal, Zhang, Cuihua, Ungvari, Zoltan·2009·American Journal of Physiology-Heart and Circulatory Physiology

Abstract

Pathways that regulate mitochondrial biogenesis are potential therapeutic targets for the amelioration of endothelial dysfunction and vascular disease. Resveratrol was shown to impact mitochondrial function in skeletal muscle and the liver, but its role in mitochondrial biogenesis in endothelial cells remains poorly defined. The present study determined whether resveratrol induces mitochondrial biogenesis in cultured human coronary arterial endothelial cells (CAECs). In CAECs resveratrol increased mitochondrial mass and mitochondrial DNA content, upregulated protein expression of electron transport chain constituents, and induced mitochondrial biogenesis factors (proliferator-activated receptor-coactivator-1α, nuclear respiratory factor-1, mitochondrial transcription factor A). Sirtuin 1 (SIRT1) was induced, and endothelial nitric oxide (NO) synthase (eNOS) was upregulated in a SIRT1-dependent manner. Knockdown of SIRT1 (small interfering RNA) or inhibition of NO synthesis prevented resveratrol-induced mitochondrial biogenesis. In aortas of type 2 diabetic (db/db) mice impaired mitochondrial biogenesis was normalized by chronic resveratrol treatment, showing the in vivo relevance of our findings. Resveratrol increases mitochondrial content in endothelial cells via activating SIRT1. We propose that SIRT1, via a pathway that involves the upregulation of eNOS, induces mitochondrial biogenesis. Resveratrol induced mitochondrial biogenesis in the aortas of type 2 diabetic mice, suggesting the potential for new treatment approaches targeting endothelial mitochondria in metabolic diseases.

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Crossref · 10.1152/ajpheart.00368.2009

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Metadata

Authors
Csiszar, A., Labinskyy, N., Pinto, J. T., Ballabh, P., Zhang, H., Losonczy, G., Pearson, K., de Cabo, R., Pacher, P., Zhang, C., & Ungvari, Z.
Venue
American Journal of Physiology-Heart and Circulatory Physiology
Published
2009-07
Volume
297
Issue
1
Pages
H13-H20
ISSN
  • 0363-6135 (ISSN-L)
  • 1522-1539
OpenAlex
W2133897047
Cited by
449
References
12
FWCI
21.67
Type
journal article
Language
en
Open access
green

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