Role of cellular compartmentation in the metabolic response to stress: Mechanistic insights from computational models

Academic Article

Abstract

  • The mechanisms controlling ATP generation in the transition from normal resting conditions to either high work states or ischemia are poorly understood. ATP generation depends upon compartmentation between the mitochondria and cytosol of metabolic pathways and key energy transfer species that cannot be easily assessed experimentally. We developed a multicompartment mathematical model of cardiac metabolism to simulate the metabolic responses to ischemia and increased workload. The model is based on mass balances, transport, and metabolic processes in cardiac tissue, and has three distinct compartments (blood, cytosol, and mitochondria). In addition to distinguishing between cytosol and mitochondria, the model includes a cytosolic subcompartment for glycolytic metabolic channeling. The model simulations predict the rapid activation of glycogenolysis and lactate production at the onset of ischemia, and support the concept of localization of glycolysis to a cytosolic subcompartment. In addition, simulations show that mitochondrial NADH/NAD + is primarily determined by oxygen consumption during ischemia, while cytosolic NADH/NAD+ and lactate production are largely a function of glycolytic flux during the initial phase, and is controlled by mitochondrial NADH/NAD+ and the malate-aspartate shuttle during the steady state. Finally, the model predicts that metabolic activation with an abrupt increase in workload requires parallel activation of ATP hydrolysis, glycolysis, mitochondrial dehydrogenases, the electron transport chain, and ADP phosphorylation. Taken together, these studies demonstrate the importance of metabolic compartmentation in the regulation of cardiac energetics in response to acute stress, and they highlight the usefulness of computational models in this line of investigation. © 2006 New York Academy of Sciences.
  • Authors

    Digital Object Identifier (doi)

    Author List

  • Zhou L; Yu X; Cabrera ME; Stanley WC
  • Start Page

  • 120
  • End Page

  • 139
  • Volume

  • 1080