Metabolic reprogramming via PPARα signaling in cardiac hypertrophy and failure: From metabolomics to epigenetics

被引:48
作者
Warren, Junco Shibayama [1 ,2 ]
Oka, Shin-ichi [3 ]
Zablocki, Daniela [3 ]
Sadoshima, Junichi [3 ]
机构
[1] Univ Utah, Nora Eccles Harrison Cardiovasc Res & Training In, Salt Lake City, UT 84112 USA
[2] Univ Utah, Sch Med, Dept Internal Med, Salt Lake City, UT 84112 USA
[3] Rutgers New Jersey Med Sch, Dept Cell Biol & Mol Med, Newark, NJ USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2017年 / 313卷 / 03期
基金
美国国家卫生研究院;
关键词
fatty acids; deoxyribonucleotide; metabolism; peroxisome proliferator-activated; receptor-alpha; ACTIVATED RECEPTOR-ALPHA; FATTY-ACID-METABOLISM; INDUCED HEART-FAILURE; MITOCHONDRIAL ENERGY-PRODUCTION; THYROID-HORMONE RECEPTOR; GENE-EXPRESSION; CONTRACTILE DYSFUNCTION; PROTEIN-KINASE; TRANSCRIPTION FACTORS; INSULIN-RESISTANCE;
D O I
10.1152/ajpheart.00103.2017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Studies using omicsbased approaches have advanced our knowledge of metabolic remodeling in cardiac hypertrophy and failure. Metabolomic analysis of the failing heart has revealed global changes in mitochondrial substrate metabolism. Peroxisome proliferator-activated receptor-alpha (PPAR alpha) plays a critical role in synergistic regulation of cardiac metabolism through transcriptional control. Metabolic reprogramming via PPAR alpha signaling in heart failure ultimately propagates into myocardial energetics. However, emerging evidence suggests that the expression level of PPAR alpha per se does not always explain the energetic state in the heart. The transcriptional activities of PPAR alpha are dynamic, yet highly coordinated. An additional level of complexity in the PPAR alpha regulatory mechanism arises from its ability to interact with various partners, which ultimately determines the metabolic phenotype of the diseased heart. This review summarizes our current knowledge of the PPAR alpha regulatory mechanisms in cardiac metabolism and the possible role of PPAR alpha in epigenetic modifications in the diseased heart. In addition, we discuss how metabolomics can contribute to a better understanding of the role of PPAR alpha in the progression of cardiac hypertrophy and failure.
引用
收藏
页码:H584 / H596
页数:13
相关论文
共 141 条
[1]   Genomewide Analyses Define Different Modes of Transcriptional Regulation by Peroxisome Proliferator-Activated Receptor-β/δ (PPARβ/δ) [J].
Adhikary, Till ;
Kaddatz, Kerstin ;
Finkernagel, Florian ;
Schoenbauer, Anne ;
Meissner, Wolfgang ;
Scharfe, Maren ;
Jarek, Michael ;
Bloecker, Helmut ;
Mueller-Bruesselbach, Sabine ;
Mueller, Rolf .
PLOS ONE, 2011, 6 (01)
[2]   Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor α (PPARα) [J].
Aoyama, T ;
Peters, JM ;
Iritani, N ;
Nakajima, T ;
Furihata, K ;
Hashimoto, T ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5678-5684
[3]   Thyroid hormone receptor β mutants:: Dominant negative regulators of peroxisome proliferator-activated receptor γ action [J].
Araki, O ;
Ying, H ;
Furuya, F ;
Zhu, XG ;
Cheng, SY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (45) :16251-16256
[4]   Differential regulation of stimulated glucose transport by free fatty acids and PPARα or -δ agonists in cardiac myocytes [J].
Asrih, Mohamed ;
Lerch, Rene ;
Papageorgiou, Irene ;
Pellieux, Corinne ;
Montessuit, Christophe .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2012, 302 (07) :E872-E884
[5]   The Failing Heart Relies on Ketone Bodies as a Fuel [J].
Aubert, Gregory ;
Martin, Ola J. ;
Horton, Julie L. ;
Lai, Ling ;
Vega, Rick B. ;
Leone, Teresa C. ;
Koves, Timothy ;
Gardell, Stephen J. ;
Krueger, Marcus ;
Hoppel, Charles L. ;
Lewandowski, E. Douglas ;
Crawford, Peter A. ;
Muoio, Deborah M. ;
Kelly, Daniel P. .
CIRCULATION, 2016, 133 (08) :698-705
[6]   Perturbations in the gene regulatory pathways controlling mitochondrial energy production in the failing heart [J].
Aubert, Gregory ;
Vega, Rick B. ;
Kelly, Daniel P. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2013, 1833 (04) :840-847
[7]   Preferential Oxidation of Triacylglyceride-Derived Fatty Acids in Heart Is Augmented by the Nuclear Receptor PPARα [J].
Banke, Natasha H. ;
Wende, Adam R. ;
Leone, Teresa C. ;
O'Donnell, J. Michael ;
Abel, E. Dale ;
Kelly, Daniel P. ;
Lewandowski, E. Douglas .
CIRCULATION RESEARCH, 2010, 107 (02) :233-241
[8]   p38 mitogen-activated protein kinase activates peroxisome proliferator-activated receptor α -: A potential role in the cardiac metabolic stress response [J].
Barger, PM ;
Browning, AC ;
Garner, AN ;
Kelly, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (48) :44495-44501
[9]  
Barger PM, DEACTIVATION PEROXIS, DOI [10.1172/JCI9056, DOI 10.1172/JCI9056]
[10]   Evidence for Intramyocardial Disruption of Lipid Metabolism and Increased Myocardial Ketone Utilization in Advanced Human Heart Failure [J].
Bedi, Kenneth C., Jr. ;
Snyder, Nathaniel W. ;
Brandimarto, Jeffrey ;
Aziz, Moez ;
Mesaros, Clementina ;
Worth, Andrew J. ;
Wang, Linda L. ;
Javaheri, Ali ;
Blair, Ian A. ;
Margulies, Kenneth B. ;
Rame, J. Eduardo .
CIRCULATION, 2016, 133 (08) :706-716