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Fumarate is cardioprotective via activation of the Nrf2 antioxidant pathway

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Item Type:Article
Title:Fumarate is cardioprotective via activation of the Nrf2 antioxidant pathway
Creators Name:Ashrafian, H. and Czibik, G. and Bellahcene, M. and Aksentijević, D. and Smith, A.C. and Mitchell, S.J. and Dodd, M.S. and Kirwan, J. and Byrne, J.J. and Ludwig, C. and Isackson, H. and Yavari, A. and Støttrup, N.B. and Contractor, H. and Cahill, T.J. and Sahgal, N. and Ball, D.R. and Birkler, R.I.D. and Hargreaves, I. and Tennant, D.A. and Land, J. and Lygate, C.A. and Johannsen, M. and Kharbanda, R.K. and Neubauer, S. and Redwood, C. and de Cabo, R. and Ahmet, I. and Talan, M. and Günther, U.L. and Robinson, A.J. and Viant, M.R. and Pollard, P.J. and Tyler, D.J. and Watkins, H.
Abstract:The citric acid cycle (CAC) metabolite fumarate has been proposed to be cardioprotective; however, its mechanisms of action remain to be determined. To augment cardiac fumarate levels and to assess fumarate's cardioprotective properties, we generated fumarate hydratase (Fh1) cardiac knockout (KO) mice. These fumarate-replete hearts were robustly protected from ischemia-reperfusion injury (I/R). To compensate for the loss of Fh1 activity, KO hearts maintain ATP levels in part by channeling amino acids into the CAC. In addition, by stabilizing the transcriptional regulator Nrf2, Fh1 KO hearts upregulate protective antioxidant response element genes. Supporting the importance of the latter mechanism, clinically relevant doses of dimethylfumarate upregulated Nrf2 and its target genes, hence protecting control hearts, but failed to similarly protect Nrf2-KO hearts in an in vivo model of myocardial infarction. We propose that clinically established fumarate derivatives activate the Nrf2 pathway and are readily testable cytoprotective agents.
Keywords:Antioxidants, Dimethyl Fumarate, Fumarate Hydratase, Fumarates, Inbred C57BL Mice, Knockout Mice, Models Biological, Myocardial Infarction, NF-E2-Related Factor 2, Signal Transduction, Animals, Mice
Source:Cell Metabolism
Publisher:Cell Press
Page Range:361-371
Date:7 March 2012
Official Publication:https://doi.org/10.1016/j.cmet.2012.01.017
PubMed:View item in PubMed

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