Literature DB >> 28646031

Metabolism and acetylation contribute to leucine-mediated inhibition of cardiac glucose uptake.

Edith Renguet1, Audrey Ginion1, Roselle Gélinas1, Laurent Bultot1, Julien Auquier1, Isabelle Robillard Frayne2, Caroline Daneault2, Jean-Louis Vanoverschelde1,3, Christine Des Rosiers2,4, Louis Hue5, Sandrine Horman1, Christophe Beauloye1,3, Luc Bertrand6.   

Abstract

High plasma leucine levels strongly correlate with type 2 diabetes. Studies of muscle cells have suggested that leucine alters the insulin response for glucose transport by activating an insulin-negative feedback loop driven by the mammalian target of rapamycin/p70 ribosomal S6 kinase (mTOR/p70S6K) pathway. Here, we examined the molecular mechanism involved in leucine's action on cardiac glucose uptake. Leucine was indeed able to curb glucose uptake after insulin stimulation in both cultured cardiomyocytes and perfused hearts. Although leucine activated mTOR/p70S6K, the mTOR inhibitor rapamycin did not prevent leucine's inhibitory action on glucose uptake, ruling out the contribution of the insulin-negative feedback loop. α-Ketoisocaproate, the first metabolite of leucine catabolism, mimicked leucine's effect on glucose uptake. Incubation of cardiomyocytes with [13C]leucine ascertained its metabolism to ketone bodies (KBs), which had a similar negative impact on insulin-stimulated glucose transport. Both leucine and KBs reduced glucose uptake by affecting translocation of glucose transporter 4 (GLUT4) to the plasma membrane. Finally, we found that leucine elevated the global protein acetylation level. Pharmacological inhibition of lysine acetyltransferases counteracted this increase in protein acetylation and prevented leucine's inhibitory action on both glucose uptake and GLUT4 translocation. Taken together, these results indicate that leucine metabolism into KBs contributes to inhibition of cardiac glucose uptake by hampering the translocation of GLUT4-containing vesicles via acetylation. They offer new insights into the establishment of insulin resistance in the heart.NEW & NOTEWORTHY Catabolism of the branched-chain amino acid leucine into ketone bodies efficiently inhibits cardiac glucose uptake through decreased translocation of glucose transporter 4 to the plasma membrane. Leucine increases protein acetylation. Pharmacological inhibition of acetylation reverses leucine's action, suggesting acetylation involvement in this phenomenon.Listen to this article's corresponding podcast at http://ajpheart.podbean.com/e/leucine-metabolism-inhibits-cardiac-glucose-uptake/.
Copyright © 2017 the American Physiological Society.

Entities:  

Keywords:  glucose transporter 4; glucose uptake; insulin resistance; ketone bodies; leucine; mammalian target of rapamycin; protein acetylation

Mesh:

Substances:

Year:  2017        PMID: 28646031     DOI: 10.1152/ajpheart.00738.2016

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  10 in total

1.  Statistical considerations in reporting cardiovascular research.

Authors:  Merry L Lindsey; Gillian A Gray; Susan K Wood; Douglas Curran-Everett
Journal:  Am J Physiol Heart Circ Physiol       Date:  2018-07-20       Impact factor: 4.733

Review 2.  Role of Posttranslational Modifications of Proteins in Cardiovascular Disease.

Authors:  Yong-Ping Liu; Tie-Ning Zhang; Ri Wen; Chun-Feng Liu; Ni Yang
Journal:  Oxid Med Cell Longev       Date:  2022-07-09       Impact factor: 7.310

3.  Branched-chain ketoacid overload inhibits insulin action in the muscle.

Authors:  Dipsikha Biswas; Khoi T Dao; Angella Mercer; Andrew M Cowie; Luke Duffley; Yassine El Hiani; Petra C Kienesberger; Thomas Pulinilkunnil
Journal:  J Biol Chem       Date:  2020-09-02       Impact factor: 5.157

4.  New insight in understanding the contribution of SGLT1 in cardiac glucose uptake: evidence for a truncated form in mice and humans.

Authors:  Laura Ferté; Alice Marino; Sylvain Battault; Laurent Bultot; Anne Van Steenbergen; Anne Bol; Julien Cumps; Audrey Ginion; Hermann Koepsell; Laure Dumoutier; Louis Hue; Sandrine Horman; Luc Bertrand; Christophe Beauloye
Journal:  Am J Physiol Heart Circ Physiol       Date:  2021-01-08       Impact factor: 4.733

Review 5.  Insulin signaling in the heart.

Authors:  E Dale Abel
Journal:  Am J Physiol Endocrinol Metab       Date:  2021-05-31       Impact factor: 5.900

Review 6.  Loss of Metabolic Flexibility in the Failing Heart.

Authors:  Qutuba G Karwi; Golam M Uddin; Kim L Ho; Gary D Lopaschuk
Journal:  Front Cardiovasc Med       Date:  2018-06-06

Review 7.  Cardiac metabolism as a driver and therapeutic target of myocardial infarction.

Authors:  Coert J Zuurbier; Luc Bertrand; Christoph R Beauloye; Ioanna Andreadou; Marisol Ruiz-Meana; Nichlas R Jespersen; Duvaraka Kula-Alwar; Hiran A Prag; Hans Eric Botker; Maija Dambrova; Christophe Montessuit; Tuuli Kaambre; Edgars Liepinsh; Paul S Brookes; Thomas Krieg
Journal:  J Cell Mol Med       Date:  2020-05-08       Impact factor: 5.310

Review 8.  The Regulation of Insulin-Stimulated Cardiac Glucose Transport via Protein Acetylation.

Authors:  Edith Renguet; Laurent Bultot; Christophe Beauloye; Sandrine Horman; Luc Bertrand
Journal:  Front Cardiovasc Med       Date:  2018-06-12

9.  Transplantation of adipose tissue lacking PAI-1 improves glucose tolerance and attenuates cardiac metabolic abnormalities in high-fat diet-induced obesity.

Authors:  Sijing Liu; Yi Li; Xin Fan; Kai Li; Chunrong Xu; Liping Zhang; Mao Luo; Liqun Wang; Rong Li; Jianbo Wu
Journal:  Adipocyte       Date:  2020-12       Impact factor: 4.534

Review 10.  Stable Isotopes for Tracing Cardiac Metabolism in Diseases.

Authors:  Anja Karlstaedt
Journal:  Front Cardiovasc Med       Date:  2021-11-11
  10 in total

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