Role of the malate-aspartate shuttle on the metabolic response to myocardial ischemia

JOURNAL OF THEORETICAL BIOLOGY

卷:254

Article

Lu, Ming^1,4  Zhou, Lufang^1,4  Stanley, William C.^2,4,5  Cabrera, Marco E.^1,2,3,4  Saidel, Gerald M.^1,4  Yu, Xin^1,4 

[1] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA

[2] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44106 USA

[3] Case Western Reserve Univ, Dept Pediat, Cleveland, OH 44106 USA

[4] Case Western Reserve Univ, Ctr Modeling Integrated Metab Syst, Cleveland, OH 44106 USA

[5] Univ Maryland, Div Cardiol, Dept Med, Baltimore, MD USA

关键词: malate-aspartate shuttle;    metabolic compartmentation;    mathematical modeling;    myocardial ischemia;   

DOI  :  10.1016/j.jtbi.2008.05.033

来源: Elsevier

【 摘 要 】

The malate-aspartate (M-A) shuttle provides an important mechanism to regulate glycolysis and lactate metabolism in the heart by transferring reducing equivalents from cytosol into mitochondria. However, experimental characterization of the M-A shuttle has been incomplete because of limitations in quantifying cytosolic and mitochondrial metabolites. In this study, we developed a multicompartment model of cardiac metabolism with detailed presentation of the M-A shuttle to quantitatively predict non-observable fluxes and metabolite concentrations under normal and ischemic conditions in vivo. Model simulations predicted that the M-A shuttle is functionally localized to a subdomain that spans the mitochondrial and cytosolic spaces. With the onset of ischemia, the M-A shuttle flux rapidly decreased to a new steady state in proportion to the reduction in blood flow. Simulation results suggest that the reduced M-A shuttle flux during ischemia was not due to changes in shuttle-associated enzymes and transporters. However, there was a redistribution of shuttle-associated metabolites in both cytosol and mitochondria. Therefore, the dramatic acceleration in glycolysis and the switch to lactate production that occur immediately after the onset of ischemia is mediated by reduced M-A shuttle flux through metabolite redistribution of shuttle associated species across the mitochondrial membrane. (C) 2008 Elsevier Ltd. All rights reserved.

【 授权许可】

Free