Item Type: | Article |
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Title: | NAD(+) repletion reverses heart failure with preserved ejection fraction |
Creators Name: | Tong, D., Schiattarella, G.G., Jiang, N., Altamirano, F., Szweda, P.A., Elnwasany, A., Lee, D.I., Yoo, H., Kass, D.A., Szweda, L.I., Lavandero, S., Verdin, E., Gillette, T.G. and Hill, J.A. |
Abstract: | RATIONALE: Heart failure with preserved ejection fraction (HFpEF) is a mortal clinical syndrome without effective therapies. We recently demonstrated in mice that a combination of metabolic and hypertensive stress recapitulates key features of human HFpEF. OBJECTIVE: Using this novel preclinical HFpEF model, we set out to define and manipulate metabolic dysregulations occurring in HFpEF myocardium. METHODS AND RESULTS: We observed impairment in mitochondrial fatty acid oxidation associated with hyperacetylation of key enzymes in the pathway. Down-regulation of sirtuin 3 and deficiency of NAD(+) secondary to an impaired NAD(+) salvage pathway contribute to this mitochondrial protein hyperacetylation. Impaired expression of genes involved in NAD(+) biosynthesis was confirmed in cardiac tissue from HFpEF patients. Supplementing HFpEF mice with nicotinamide riboside or a direct activator of NAD(+) biosynthesis led to improvement in mitochondrial function and amelioration of the HFpEF phenotype. CONCLUSIONS: Collectively, these studies demonstrate that HFpEF is associated with myocardial mitochondrial dysfunction and unveil NAD(+) repletion as a promising therapeutic approach in the syndrome. |
Keywords: | Heart Failure with Preserved Ejection Fraction, Mitochondria, Acetylation, Cardiomyopathy, Heart Failure, Animals, Mice |
Source: | Circulation Research |
ISSN: | 0009-7330 |
Publisher: | American Heart Association |
Volume: | 128 |
Number: | 11 |
Page Range: | 1629-1641 |
Date: | 28 May 2021 |
Additional Information: | Copyright © 2021 American Heart Association, Inc. |
Official Publication: | https://doi.org/10.1161/CIRCRESAHA.120.317046 |
External Fulltext: | View full text on PubMed Central |
PubMed: | View item in PubMed |
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