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A Quantitative Study of Oxygen as a Metabolic RegulatorAn acute reduction in oxygen delivery to a tissue is associated with metabolic changes aimed at maintaining ATP homeostasis. However, given the complexity of the human bio-energetic system, it is difficult to determine quantitatively how cellular metabolic processes interact to maintain ATP homeostasis during stress (e.g., hypoxia, ischemia, and exercise). In particular, we are interested in determining mechanisms relating cellular oxygen concentration to observed metabolic responses at the cellular, tissue, organ, and whole body levels and in quantifying how changes in tissue oxygen availability affect the pathways of ATP synthesis and the metabolites that control these pathways. In this study; we extend a previously developed mathematical model of human bioenergetics, to provide a physicochemical framework that permits quantitative understanding of oxygen as a metabolic regulator. Specifically, the enhancement - sensitivity analysis - permits studying the effects of variations in tissue oxygenation and parameters controlling cellular respiration on glycolysis, lactate production, and pyruvate oxidation. The analysis can distinguish between parameters that must be determined accurately and those that require less precision, based on their effects on model predictions. This capability may prove to be important in optimizing experimental design, thus reducing use of animals.
Document ID
20040046945
Acquisition Source
Headquarters
Document Type
Reprint (Version printed in journal)
Authors
Radhakrishnan, Krishnan
(NASA Glenn Research Center Cleveland, OH, United States)
LaManna, Joseph C.
(Case Western Reserve Univ. Cleveland, OH, United States)
Cabera, Marco E.
(Rainbow Babies and Children's Hospital Cleveland, OH, United States)
Date Acquired
August 21, 2013
Publication Date
January 1, 2000
Publication Information
Publication: Applied Cardiopulmonary Pathophysiology
Publisher: Pabst Science Publishers
Volume: 9
Issue: 4
ISBN: 3-933151-79-1
Subject Category
Life Sciences (General)
Funding Number(s)
CONTRACT_GRANT: NCC3-782
CONTRACT_GRANT: NCC3-622
CONTRACT_GRANT: NHLBI-HL-58653-01A1
Distribution Limits
Public
Copyright
Other

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