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1 Department of Medicine, University of California, San Diego, and 3 San Diego Veterans Administration Health Care System and Department of Radiology, University of California, San Diego, La Jolla 92093-0623; and 2 Huntington Medical Research Institute, Pasadena, California 91105
A noninvasive magnetic
resonance imaging (MRI) method to assess the distribution of perfusion
and metabolic demand (
/
O2) in
exercising human skeletal muscle is described. This method combines two
MRI techniques that can provide accurate multiple localized
measurements of
/
O2 during
steady-state plantar flexion exercise. The first technique,
31P chemical shift imaging, permits the acquisition of
comparable phosphorus spectra from multiple voxels simultaneously.
Because phosphocreatine (PCr) depletion is directly proportional to ATP hydrolysis, its relative depletion can be used as an index of muscle
O2 uptake (
O2). The second
MRI technique allows the measurement of both spatially and temporally
resolved muscle perfusion in vivo by using arterial spin labeling.
Promising validity and reliability data are presented for both MRI
techniques. Initial results from the combined method provide evidence
of a large variation in
/
O2, revealing areas of apparent under- and overperfusion for a given metabolic turnover. Analysis of these data in a similar fashion to that
employed in the assessment of ventilation-to-perfusion matching in the
lungs revealed a similar second moment of the perfusion distribution
and PCr distribution on a log scale (log SD
and log
SDPCr) (0.47). Modeling the effect of variations in
log SD
and log SDPCr in terms of
attainable
O2, assuming no diffusion limits, indicates that the log SD
and log
SDPCr would allow only 92% of the target
O2 to be achieved. This communication
documents this novel, noninvasive method for assessing
/
O2, and initial data suggest
that the mismatch in
/
O2 may play
a significant role in determining O2 transport and
utilization during exercise.
arterial spin labeling; chemical shift imaging; blood flow; metabolism; magnetic resonance imaging
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