Purpose: To develop a noninvasive protocol for measuring local perfusion and metabolic demand in muscle tissue with sufficient sensitivity and time resolution to monitor kinetics at the onset of low-level exercise and during recovery.
Materials and Methods:Capillary-level perfusion, the critical factor that determines oxygen and substrate delivery to active muscle, was measured by an arterial spin labeling (ASL) technique optimized for skeletal muscle. Phosphocreatine (PCr) kinetics, which signal the flux of oxidative phosphorylation, were measured by 31 P MR spectroscopy. Perfusion and PCr measurements were made in parallel studies before, during, and after three different intensities of low-level, stimulated exercise in rat hind limb.
Results:The data reveal close coupling between the perfusion response and PCr changes. The onset and recovery time constants for PCr changes were independent of contractile force over the range of forces studied. Perfusion time constants during both onset of exercise and recovery tended to increase with contractile force.
Conclusion:These results demonstrate that the protocol implemented can be useful for probing the mechanisms that control skeletal muscle blood flow, the physiological limits to muscle performance, and the causes for the attenuated exercise-induced hyperemia observed in disease states. IN THIS WORK we describe a noninvasive protocol for acquiring parallel perfusion measurements and 31 P magnetic resonance spectroscopy (MRS) measurements of high-energy phosphorous metabolites in skeletal muscle with sufficient time resolution and sensitivity to monitor kinetics at the onset of low-level exercise and during recovery. Our research group has previously developed a quantitative, magnetic resonance (MR)-based perfusion measurement technique that is particularly well suited for skeletal muscle (1-3). This technique, flow-driven arterial water stimulation with elimination of tissue signal (FAWSETS), is a form of arterial spin labeling (ASL). In this work we have combined FAWSETS perfusion measurements with standard 31 P-MRS measurements of metabolic activity. Our primary goal was to achieve adequate time resolution to determine the time-course of perfusion and phosphocreatine (PCr) changes during entire cycles of exercise and recovery. Our secondary goal was to probe the limits of sensitivity to perfusion for the FAWSETS technique at low intensity exercise.In normal subjects, skeletal muscle blood flow increases rapidly during exercise and achieves a steady state that is dependent on metabolic demand (4,5). Exercise-related increases in muscle perfusion are attenuated in a number of diseases, including insulin resistance and diabetes (6 -8), congestive heart failure (9 -11), compartment syndrome (12,13), peripheral vascular disease (PVD) (14,15), and systemic sclerosis (scleroderma) (16). It is likely that the exercise intolerance, muscle fatigue, and atrophy related to these diseases arise from insufficient delivery of oxygen and substrates to meet metabolic demands dur...