Abstract
A high fat diet (HFD) induces substantial cardiac metabolic alteration(s), but the initiating molecular events remain unclear. We assessed the early cardiac energy metabolic changes in C57/BJ mice fed a HFD for 10days. Carbohydrate oxidation was markedly decreased in mice on a HFD, in which up-regulation of pyruvate dehydrogenase kinase 4 (PDK4) was evident. Concurrently, E2F1, a transcription factor controlling PDK4 expression, was activated, as was cyclin D1, an upstream-molecule of E2F1, and eukaryotic initiation factor 4E (eIF4E), a modulator of cyclinD1 translation. Hence, HFD may initiate early cardiac metabolic alterations through the eIF4E/cyclin D1/E2F1/PDK4 axis.
Copyright © 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cell Nucleus / metabolism
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Cyclin D1 / genetics
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Cyclin D1 / metabolism
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Cyclin-Dependent Kinase 4 / genetics
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Cyclin-Dependent Kinase 4 / metabolism
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Diet, High-Fat / adverse effects*
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E2F1 Transcription Factor / genetics
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E2F1 Transcription Factor / metabolism*
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Energy Metabolism*
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Eukaryotic Initiation Factor-2 / metabolism
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Eukaryotic Initiation Factor-4E / metabolism
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Male
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Mice
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Mice, Inbred C57BL
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Myocardium / enzymology
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Myocardium / metabolism*
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Oxidation-Reduction
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Phosphorylation
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Protein Processing, Post-Translational
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Protein Serine-Threonine Kinases / metabolism*
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Protein Transport
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Pyruvate Dehydrogenase Acetyl-Transferring Kinase
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RNA, Messenger / metabolism
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Signal Transduction*
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Time Factors
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Up-Regulation*
Substances
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Ccnd1 protein, mouse
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E2F1 Transcription Factor
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E2f1 protein, mouse
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Eukaryotic Initiation Factor-2
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Eukaryotic Initiation Factor-4E
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Pdk4 protein, mouse
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Pyruvate Dehydrogenase Acetyl-Transferring Kinase
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RNA, Messenger
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Cyclin D1
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Protein Serine-Threonine Kinases
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Cdk4 protein, mouse
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Cyclin-Dependent Kinase 4