Compartment model for measuring myocardial oxygen consumption using [1-11C]acetate

J Nucl Med. 1997 Mar;38(3):459-66.

Abstract

Although [1-11C]acetate has been validated as a PET tracer for myocardial oxygen consumption (MVO2) in animals and humans, mono- and biexponential fitting of the tissue time-activity curve yields only estimates of MVO2. This study attempts to develop and validate a simple tracer kinetic model in vivo for estimation of regional MVO2.

Methods: Twenty-seven experiments were performed in 12 anesthetized dogs with [1-11C]acetate and serial PET images under different MBF and MVO2 (baseline, ischemia, xylazine, dobutamine and dipyridamole). Estimates of MVO2 were obtained from dynamic [1-11C]acetate PET and model fitting. MBF was measured by radiolabeled microspheres, and MVO2 was calculated by the Fick method using arterial and coronary blood samples.

Results: The proposed model fitted equally well for all study conditions with a multiple correlation coefficient of 0.985 +/- 0.026. Estimated MVO2 correlated linearly with measured MVO2 (y = 0.033 + 0.690x, r = 0.92, s.e. of estimates = 0.020).

Conclusion: This study indicates that MVO2 can be assessed with PET and [1-11C]acetate over a wide range with a simple tracer kinetic model.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetates / blood
  • Animals
  • Body Fluid Compartments
  • Carbon Dioxide / blood
  • Carbon Radioisotopes
  • Chi-Square Distribution
  • Computer Simulation
  • Coronary Circulation
  • Dipyridamole
  • Dobutamine
  • Dogs
  • Fatty Acids, Nonesterified / metabolism
  • Models, Cardiovascular*
  • Myocardium / metabolism*
  • Oxygen Consumption / physiology*
  • Tomography, Emission-Computed
  • Xylazine

Substances

  • Acetates
  • Carbon Radioisotopes
  • Fatty Acids, Nonesterified
  • Carbon Dioxide
  • Xylazine
  • Dobutamine
  • Dipyridamole