Myocardial Ketones Metabolism in Heart Failure

Qutuba G. Karwi, Dipsikha Biswas, Thomas Pulinilkunnil, Gary D. Lopaschuk

Research output: Contribution to journalReview articlepeer-review

53 Citations (Scopus)

Abstract

Ketone bodies can become a major source of adenosine triphosphate production during stress to maintain bioenergetic homeostasis in the brain, heart, and skeletal muscles. In the normal heart, ketone bodies contribute from 10% to 15% of the cardiac adenosine triphosphate production, although their contribution during pathologic stress is still not well-characterized and currently represents an exciting area of cardiovascular research. This review focuses on the mechanisms that regulate circulating ketone levels under physiologic and pathologic conditions and how this impacts cardiac ketone metabolism. We also review the current understanding of the role of augmented ketone metabolism as an adaptive response in different types and stages of heart failure. This analysis includes the emerging experimental and clinical evidence of the potential favorable effects of boosting ketone metabolism in the failing heart and the possible mechanisms of action through which these interventions may mediate their cardioprotective effects. We also critically appraise the emerging data from animal and human studies which characterize the role of ketones in mediating the cardioprotection established by the new class of antidiabetic drugs, namely sodium-glucose co-transporter inhibitors.

Original languageEnglish
Pages (from-to)998-1005
Number of pages8
JournalJournal of Cardiac Failure
Volume26
Issue number11
DOIs
Publication statusPublished - Nov 2020

Bibliographical note

Funding Information:
Supported by a Canadian Institutes for Health Research Foundation grant, a Heart and Stroke Foundation of Canada grant and an Alberta Heritage Foundation for Medical Research Scientist Award to G. D. L. and by the University Hospital Foundation. This work was also funded by grants to T.C.P from the Natural Sciences and Engineering Research Council of Canada (RGPIN-2014-03687), Diabetes Canada (NOD_OG-3-15-5037-TP, NOD_SC-5-16-5054-TP), the Beatrice Hunter Cancer Research Institute and the New Brunswick Health Research Foundation. D.B. is funded by Postdoctoral fellowships from the New Brunswick Health Research Foundation and Dalhousie Medicine New Brunswick. Q.G.K. is funded by Alberta Innovates Postgraduate Fellowship in Health Innovation.

Publisher Copyright:
© 2020 Elsevier Inc.

ASJC Scopus Subject Areas

  • Cardiology and Cardiovascular Medicine

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