Metabolic regulation of exercise-induced adaptation in striated muscle

Information

  • Research Project
  • 10462474
  • ApplicationId
    10462474
  • Core Project Number
    F31HL154663
  • Full Project Number
    5F31HL154663-02
  • Serial Number
    154663
  • FOA Number
    PA-19-195
  • Sub Project Id
  • Project Start Date
    8/10/2020 - 4 years ago
  • Project End Date
    8/9/2023 - a year ago
  • Program Officer Name
    HUANG, LI-SHIN
  • Budget Start Date
    8/10/2021 - 3 years ago
  • Budget End Date
    8/9/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    02
  • Suffix
  • Award Notice Date
    8/22/2021 - 3 years ago

Metabolic regulation of exercise-induced adaptation in striated muscle

Abstract Aerobic exercise promotes beneficial adaptations in the heart. Previous studies demonstrate that transient reductions in cardiac glucose catabolism at the level of phosphofructokinase are important for exercise-induced cardiac growth. Although this finding links changes in metabolism with initiation of growth, the mechanisms by which glucose metabolism changes during exercise and how metabolism coordinates cardiac growth remain unclear. Metabolic changes could promote exercise-induced muscle growth in two ways. First, changes in the levels of glycolytic intermediates during exercise could regulate carbon availability for building block biosynthesis, which constitutes a material cause for cardiomyocyte hypertrophy. Second, metabolic changes that occur during exercise could regulate the exercise gene program, which is important for exercise-induced tissue remodeling. Nevertheless, it has been difficult to disentangle the contribution of these two causes to the adaptations brought forth by exercise. Addressing these problems requires understanding how metabolism changes both during and after exercise, and then identifying the metabolic components that modulate cardiomyocyte growth. In this project, I will test the general hypothesis that high levels of competing substrates such as lactate and fatty acids prompt ancillary biosynthetic pathway activity in the heart and drive gene programs for cardiac growth. To understand how glucose metabolism changes in response to exercise or in the presence of competing substrates, I have standardized deep network tracing methods to measure glucose-derived carbon fate in vivo using dietary delivery of a 13C6-glucose-containing diet. Specifically, the aims are (1) to define changes in cardiac glucose metabolism in response to exercise training and (2) to determine how circulating substrates influence cardiac hypertrophic signaling and gene programs. This research plan will provide training in areas critical to my growth as a scientist and prepare me for a career in the exercise sciences. The project will provide fresh perspectives about how metabolism regulates cardiac muscle growth and could identify innovative metabolic approaches to control tissue remodeling or optimize the cardiovascular benefits of exercise. Importantly, these studies will integrate our current understanding of striated muscle catabolism with new knowledge of how anabolism is regulated within muscle tissue.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    F31
  • Administering IC
    HL
  • Application Type
    5
  • Direct Cost Amount
    36647
  • Indirect Cost Amount
  • Total Cost
    36647
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    837
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NHLBI:36647\
  • Funding Mechanism
    TRAINING, INDIVIDUAL
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    UNIVERSITY OF LOUISVILLE
  • Organization Department
    INTERNAL MEDICINE/MEDICINE
  • Organization DUNS
    057588857
  • Organization City
    LOUISVILLE
  • Organization State
    KY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    402920001
  • Organization District
    UNITED STATES