Re-balancing cellular energy substrate metabolism to mend the failing heart

被引:73
作者
Glatz, Jan F. C. [1 ]
Nabben, Miranda [1 ]
Young, Martin E. [2 ]
Schulze, P. Christian [3 ]
Taegtmeyer, Heinrich [4 ]
Luiken, Joost J. F. P. [1 ]
机构
[1] Maastricht Univ, Fac Hlth Med & Life Sci FHML, Dept Genet & Cell Biol, Maastricht, Netherlands
[2] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[3] Friedrich Schiller Univ Jena, Univ Hosp Jena, Dept Internal Med 1, Div Cardiol Angiol Pneumol & Intens Med Care, Jena, Germany
[4] Univ Texas Hlth Sci Ctr Houston, McGovern Med Sch, Dept Internal Med, Div Cardiol, Houston, TX 77030 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2020年 / 1866卷 / 05期
关键词
Long-chain fatty acids; Glucose; Energy homeostasis; Substrate balance; Cardiac contractile function; Heart failure; Diabetes; CITRIC-ACID CYCLE; PRESSURE-OVERLOAD; GENE-EXPRESSION; CARDIAC METABOLISM; KETONE-BODIES; FATTY-ACIDS; RAT HEARTS; FAILURE; LIPOTOXICITY; ANAPLEROSIS;
D O I
10.1016/j.bbadis.2019.165579
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fatty acids and glucose are the main substrates for myocardial energy provision. Under physiologic conditions, there is a distinct and finely tuned balance between the utilization of these substrates. Using the non-ischemic heart as an example, we discuss that upon stress this substrate balance is upset resulting in an over-reliance on either fatty acids or glucose, and that chronic fuel shifts towards a single type of substrate appear to be linked with cardiac dysfunction. These observations suggest that interventions aimed at re-balancing a tilted substrate preference towards an appropriate mix of substrates may result in restoration of cardiac contractile performance. Examples of manipulating cellular substrate uptake as a means to re-balance fuel supply, being associated with mended cardiac function underscore this concept. We also address the molecular mechanisms underlying the apparent need for a fatty acid-glucose fuel balance. We propose that re-balancing cellular fuel supply, in particular with respect to fatty acids and glucose, may be an effective strategy to treat the failing heart.
引用
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页数:8
相关论文
共 81 条
[1]   Diabetic db/db mice do not develop heart failure upon pressure overload: a longitudinal in vivo PET, MRI, and MRS study on cardiac metabolic, structural, and functional adaptations [J].
Abdurrachim, Desiree ;
Nabben, Miranda ;
Hoerr, Verena ;
Kuhlmann, Michael T. ;
Bovenkamp, Philipp ;
Ciapaite, Jolita ;
Geraets, Ilvy M. E. ;
Coumans, Will ;
Luiken, Joost J. F. P. ;
Glatz, Jan F. C. ;
Schaefers, Michael ;
Nicolay, Klaas ;
Faber, Cornelius ;
Hermann, Sven ;
Prompers, Jeanine J. .
CARDIOVASCULAR RESEARCH, 2017, 113 (10) :1148-1160
[2]   Good and bad consequences of altered fatty acid metabolism in heart failure: evidence from mouse models [J].
Abdurrachim, Desiree ;
Luiken, Joost J. F. P. ;
Nicolay, Klaas ;
Glatz, Jan F. C. ;
Prompers, Jeanine J. ;
Nabben, Miranda .
CARDIOVASCULAR RESEARCH, 2015, 106 (02) :194-205
[3]   Mitochondrial adaptations to physiological vs. pathological cardiac hypertrophy [J].
Abel, E. Dale ;
Doenst, Torsten .
CARDIOVASCULAR RESEARCH, 2011, 90 (02) :234-242
[4]   Mechanisms and Consequences of Inflammatory Signaling in the Myocardium [J].
Ahn, Jihyun ;
Kim, Jaetaek .
CURRENT HYPERTENSION REPORTS, 2012, 14 (06) :510-516
[5]   Transverse aortic constriction leads to accelerated heart failure in mice lacking PPAR-γ coactivator 1α [J].
Arany, Zoltan ;
Novikov, Mikhail ;
Chin, Sherry ;
Ma, Yanhong ;
Rosenzweig, Anthony ;
Spiegelman, Bruce M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (26) :10086-10091
[6]   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
[7]   Domestication of the cardiac mitochondrion for energy conversion [J].
Balaban, Robert S. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2009, 46 (06) :832-841
[8]   Normalizing the metabolic phenotype after myocardial infarction: Impact of subchronic high fat feeding [J].
Berthiaume, Jessica M. ;
Young, Martin E. ;
Chen, Xiaoqin ;
McElfresh, Tracy A. ;
Yu, Xin ;
Chandler, Margaret P. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2012, 53 (01) :125-133
[9]   Triacylglycerol accumulation in human obesity and type 2 diabetes is associated with increased rates of skeletal muscle fatty acid transport and increased sarcolemmal FAT/CD36 [J].
Bonen, A ;
Parolin, ML ;
Steinberg, GR ;
Calles-Escandon, J ;
Tandon, NN ;
Glatz, JFC ;
Luiken, JJFP ;
Heigenhauser, GJF ;
Dyck, DJ .
FASEB JOURNAL, 2004, 18 (07) :1144-+
[10]   My Sweetheart Is Broken: Role of Glucose in Diabetic Cardiomyopathy [J].
Brahma, Manoja K. ;
Pepin, Mark E. ;
Wende, Adam R. .
DIABETES & METABOLISM JOURNAL, 2017, 41 (01) :1-9