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Role of NAD+ and mitochondrial sirtuins in cardiac and renal diseases.


ABSTRACT: The coenzyme nicotinamide adenine dinucleotide (NAD+) has key roles in the regulation of redox status and energy metabolism. NAD+ depletion is emerging as a major contributor to the pathogenesis of cardiac and renal diseases and NAD+ repletion strategies have shown therapeutic potential as a means to restore healthy metabolism and physiological function. The pleotropic roles of NAD+ enable several possible avenues by which repletion of this coenzyme could have therapeutic efficacy. In particular, NAD+ functions as a co-substrate in deacylation reactions carried out by the sirtuin family of enzymes. These NAD+-dependent deacylases control several aspects of metabolism and a wealth of data suggests that boosting sirtuin activity via NAD+ supplementation might be a promising therapy for cardiac and renal pathologies. This Review summarizes the role of NAD+ metabolism in the heart and kidney, and highlights the mitochondrial sirtuins as mediators of some of the beneficial effects of NAD+-boosting therapies in preclinical animal models. We surmise that modulating the NAD+-sirtuin axis is a clinically relevant approach to develop new therapies for cardiac and renal diseases.

SUBMITTER: Hershberger KA 

PROVIDER: S-EPMC5508210 | biostudies-other | 2017 Apr

REPOSITORIES: biostudies-other

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Role of NAD<sup>+</sup> and mitochondrial sirtuins in cardiac and renal diseases.

Hershberger Kathleen A KA   Martin Angelical S AS   Hirschey Matthew D MD  

Nature reviews. Nephrology 20170206 4


The coenzyme nicotinamide adenine dinucleotide (NAD<sup>+</sup>) has key roles in the regulation of redox status and energy metabolism. NAD<sup>+</sup> depletion is emerging as a major contributor to the pathogenesis of cardiac and renal diseases and NAD<sup>+</sup> repletion strategies have shown therapeutic potential as a means to restore healthy metabolism and physiological function. The pleotropic roles of NAD<sup>+</sup> enable several possible avenues by which repletion of this coenzyme co  ...[more]

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