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New Insight into the Role of Myocardial Fatty Acid Uptake and Utilization in Health and Disease

  • Author / Creator
    Nagendran, Jeevan
  • All mammalian cells rely on adenosine triphosphate (ATP) to maintain function and for survival. The heart has the highest basal ATP demand of any organ due to the necessity for continuous contraction. As such, the ability of the cardiomyocyte to monitor cellular energy status and adapt the supply of substrates to match the energy demand is crucial. However, despite having basal energy demands exceeding those of any other organ in the body, cardiomyocytes do not possess large reserves of substrates required to form high-energy. As such, the heart must rely on exogenous substrate supply to be transported into the cardiomyocytes in order to be catabolized and to produce ATP. Because of this, continuous transport of substrates such as fatty acids (FAs), glucose, and lactate into the cardiomyocytes is a key component of cardiac energy metabolism. During normal physiological conditions, this production of ATP is met almost entirely (>95%) through oxidative phosphorylation. Specifically, FA oxidation is responsible for the generation of 50–70% of ATP in a normal adult heart while only 20–30% of the energy provided is derived from glucose and less than 5% from other sources. Herein, we review the involvement of myocardial FA uptake and subsequent utilization as it relates to cardiac function in physiologic and pathophysiologic processes. Specifically, we examine the cardiomyocyte-specific role of CD36, a FA transport protein, during ischemia-reperfusion injury. Utilizing an inducible cardiomyocyte-specific CD36 ablation mouse model, we provide genetic evidence that reduced FA oxidation as a result of diminished CD36-mediated FA uptake improves post-ischemic cardiac efficiency and functional recovery. As such, targeting cardiomyocyte FA uptake and FA oxidation via inhibition of CD36 in the adult myocardium may provide therapeutic benefit during ischemia-reperfusion. Furthermore, we examine the cardiomyocyte-specific role of adipose triglyceride lipase (ATGL) overexpression during doxorubicin induced cardiac dysfunction. Our data suggest that chronic reduction in myocardial triacylglycerol (TAG) content by cardiomyocyte-specific ATGL over-expression is able to prevent doxorubicin-induced cardiac dysfunction. We also examine the role of AMPK inhibitory phosphorylation of acetyl CoA carboxylase during high workload and ischemia-reperfusion injury. Our findings challenge the previously suggested role of AMPK-mediated ACC phosphorylation and inactivation as having a major role in the regulation of substrate metabolism and function in healthy and stressed myocardium. As well, since diabetes is one of the pathophysiologic processes known to cause alterations in FA metabolism in the myocardium, we further examined the effects of glucose-lowering medication on early outcomes of patients that had and acute coronary syndrome event. The work presented also emphasizes areas that require further investigation for the purpose of eventually translating this information into improved patient care.

  • Subjects / Keywords
  • Graduation date
    2013-11
  • Type of Item
    Thesis
  • Degree
    Doctor of Philosophy
  • DOI
    https://doi.org/10.7939/R36W96H9N
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
  • Language
    English
  • Institution
    University of Alberta
  • Degree level
    Doctoral
  • Department
    • Department of Medicine
  • Specialization
    • Experimental Medicine
  • Supervisor / co-supervisor and their department(s)
    • Dyck, Jason RB (Pediatrics)/ McAlister, Finlay A (Medicine)
  • Examining committee members and their departments
    • Legare, Jean-Francois (Surgery, Dalhousie University)
    • Dyck, Jason RB (Pediatrics)
    • McAlister, Finlay A (Medicine)
    • Ross, David B (Surgery)
    • Cheung, Po-Yin (Pediatrics)
    • Madsen, Karen (Medicine - exam committee chair)