Adropin Regulates Cardiac Energy Metabolism and Improves Cardiac Function and Efficiency, 2019, Lopaschuk et al

Andy · Jun 17, 2019

In mice!

Highlights

Adropin injections improve cardiac function and reduce fatty acid oxidation.

Acute adropin administration shifts energy substrate preference towards glucose.

Adropin enhances insulin signalling and activates pyruvate dehydrogenase.

Abstract
Background
Impaired cardiac insulin signalling and high cardiac fatty acid oxidation rates are characteristics of conditions of insulin resistance and diabetic cardiomyopathies. The potential role of liver-derived peptides such as adropin in mediating these changes in cardiac energy metabolism is unclear, despite the fact that in skeletal muscle adropin can preferentially promote glucose metabolism and improve insulin sensitivity.

Objectives
To determine the influence of adropin on cardiac energy metabolism, insulin signalling and cardiac efficiency.

Methods
C57Bl/6 mice were injected with either vehicle or a secretable form of adropin (450 nmol/kg, i.p.) three times over a 24-h. period. The mice were fasted to accentuate the differences between animals in adropin plasma levels before their hearts were isolated and perfused using a working heart system. In addition, direct addition of adropin to the perfusate of ex vivo hearts isolated from non-fasting mice was utilized to investigate the acute effects of the peptide on heart metabolism and ex vivo function.

Results
In contrast to the observed fasting-induced predominance of fatty acid oxidation as a source of ATP production in control hearts, insulin inhibition of fatty acid oxidation was preserved by adropin treatment. Adropin-treated mouse hearts also showed a higher cardiac work, which was accompanied by improved cardiac efficiency and enhanced insulin signalling compared to control hearts. Interestingly, acute adropin administration to isolated working hearts also resulted in an inhibition of fatty acid oxidation, accompanied by a robust stimulation of glucose oxidation compared to vehicle-treated hearts. Adropin also increased activation of downstream cardiac insulin signalling. Moreover, both in vivo and ex vivo treatment protocols induced a reduction in the inhibitory phosphorylation of pyruvate dehydrogenase (PDH), the major enzyme of glucose oxidation, and the protein levels of the responsible kinase PDH kinase 4 and the insulin-signalling inhibitory phosphorylation of JNK (p-T183/Y185) and IRS-1 (p-S307), suggesting acute receptor- and/or post-translational modification-mediated mechanisms.

Conclusions
These results demonstrate that adropin has important effects on energy metabolism in the heart and may be a putative candidate for the treatment of cardiac disease associated with impaired insulin sensitivity.
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Paywall, https://www.metabolismjournal.com/article/S0026-0495(19)30114-3/abstract
Sci hub, paper not available at time of posting

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Adropin Regulates Cardiac Energy Metabolism and Improves Cardiac Function and Efficiency, 2019, Lopaschuk et al

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Adropin Regulates Cardiac Energy Metabolism and Improves Cardiac Function and Efficiency, 2019, Lopaschuk et al

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