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      Retinoic acid regulates pyruvate dehydrogenase kinase 4 ( Pdk4) to modulate fuel utilization in the adult heart: Insights from wild‐type and β‐carotene 9′,10′ oxygenase knockout mice

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          Abstract

          Regulation of the pyruvate dehydrogenase (PDH) complex by the pyruvate dehydrogenase kinase PDK4 enables the heart to respond to fluctuations in energy demands and substrate availability. Retinoic acid, the transcriptionally active form of vitamin A, is known to be involved in the regulation of cardiac function and growth during embryogenesis as well as under pathological conditions. Whether retinoic acid also maintains cardiac health under physiological conditions is unknown. However, vitamin A status and intake of its carotenoid precursor β‐carotene have been linked to the prevention of heart diseases. Here, we provide in vitro and in vivo evidence that retinoic acid regulates cardiac Pdk4 expression and thus PDH activity. Furthermore, we show that mice lacking β‐carotene 9′,10′‐oxygenase (BCO2), the only enzyme of the adult heart that cleaves β‐carotene to generate retinoids (vitamin A and its derivatives), displayed cardiac retinoic acid insufficiency and impaired metabolic flexibility linked to a compromised PDK4/PDH pathway. These findings provide novel insights into the functions of retinoic acid in regulating energy metabolism in adult tissues, especially the heart.

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          A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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            A simple method for the isolation and purification of total lipides from animal tissues.

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              A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation

              Over the years, the mitochondrial fatty acid β-oxidation (FAO) pathway has been characterised at the biochemical level as well as the molecular biological level. FAO plays a pivotal role in energy homoeostasis, but it competes with glucose as the primary oxidative substrate. The mechanisms behind this so-called glucose–fatty acid cycle operate at the hormonal, transcriptional and biochemical levels. Inherited defects for most of the FAO enzymes have been identified and characterised and are currently included in neonatal screening programmes. Symptoms range from hypoketotic hypoglycaemia to skeletal and cardiac myopathies. The pathophysiology of these diseases is still not completely understood, hampering optimal treatment. Studies of patients and mouse models will contribute to our understanding of the pathogenesis and will ultimately lead to better treatment.
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                Author and article information

                Contributors
                lquadro@sebs.rutgers.edu
                Journal
                FASEB J
                FASEB J
                10.1096/(ISSN)1530-6860
                FSB2
                The FASEB Journal
                John Wiley and Sons Inc. (Hoboken )
                0892-6638
                1530-6860
                25 August 2022
                September 2022
                : 36
                : 9 ( doiID: 10.1096/fsb2.v36.9 )
                : e22513
                Affiliations
                [ 1 ] Graduate Program in Endocrinology and Animal Bioscience Rutgers University New Brunswick New Jersey USA
                [ 2 ] Department of Food Science Rutgers University New Brunswick New Jersey USA
                [ 3 ] Rutgers Center for Lipid Research and Institute of Food Nutrition and Health Rutgers University New Brunswick New Jersey USA
                [ 4 ] Department of Pharmaceutics Health Sciences University of Washington Seattle Washington USA
                [ 5 ] Department of Nutritional Sciences Rutgers University New Brunswick New Jersey USA
                Author notes
                [*] [* ] Correspondence

                Loredana Quadro, Department of Food Science, Rutgers University, 65 Dudley Road, New Brunswick, NJ 08901, USA.

                Email: lquadro@ 123456sebs.rutgers.edu

                Author information
                https://orcid.org/0000-0002-2811-9594
                Article
                FSB222513 202101910RR
                10.1096/fj.202101910RR
                9544431
                36004605
                401d3f06-ba12-4bf4-9bef-df593f8d880d
                © 2022 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 05 August 2022
                : 15 December 2021
                : 11 August 2022
                Page count
                Figures: 7, Tables: 2, Pages: 20, Words: 12391
                Funding
                Funded by: HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
                Award ID: R01 HD094778
                Funded by: HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) , doi 10.13039/100000062;
                Award ID: DK126963
                Funded by: HHS | NIH | National Institute of General Medical Sciences (NIGMS) , doi 10.13039/100000057;
                Award ID: GM111772
                Funded by: NIH F31 Ruth Kirschstein Predoctoral individual research award
                Award ID: 1F31HL143930
                Funded by: Rutgers Center for Lipid Research small grant program
                Funded by: USDA, Hatch Project , doi 10.13039/100000199;
                Award ID: 1018402
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                September 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.0 mode:remove_FC converted:07.10.2022

                Molecular biology
                heart,metabolic flexibility,retinoic acid,β‐carotene 9′,10′‐dioxygenase

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