Nonmonoexponential MR diffusion decay behavior has been observed at high di
ffusion-weighting strengths for cell aggregates and tissues, including the
myocardium; however, implications for myocardial MR diffusion tenser imagin
g are largely unknown. In this study, a slow-exchange-limit, two-component
diffusion tenser model was fitted to diffusion-weighted images obtained in
isolated, perfused rat hearts. Results indicate that there are at least two
distinct components of anisotropic diffusion, characterized by a "fast" co
mponent whose principal diffusivity is comparable to that of the perfusate,
and a highly anisotropic "slow" component. It is speculated that the two c
omponents correspond to tissue compartments and have a general agreement wi
th the orientations of anisotropy, or fiber orientations, in the myocardium
. Moreover, consideration of previous studies of myocardial diffusion sugge
sts that the presently observed fast component may likely be dominated by d
iffusion in the vascular space, whereas the slow component may include the
intracellular and interstitial compartments. The implications of the result
s for myocardial fiber orientation mapping and limitations of the current t
wo-component model used are also discussed. (C) 2001 Wiley-Liss, Inc.