Simultaneous Assessment of Skeletal Muscle Energetics and Blood Flow During Dynamic Exercise by Interleaved
T Jake Samuel1, Sandeep K Ganji2,3, Joseph R Goldenberg4
1Division of Magnetic Resonance Research, Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Purpose:
To simultaneously measure skeletal muscle energetics and blood flow (BF) before, during, and after dynamic plantar flexion exercise (PFE).
Methods:
Non-localized pulse-acquire phosphorus-31 magnetic resonance spectroscopy (31P MRS) and phase contrast flow magnetic resonance imaging (1H MRI) using golden-angle rotated spiral readouts were acquired in an interleaved fashion. Data were collected at rest, during PFE to volitional fatigue, and post-exercise recovery in 10 healthy adults. Interleaved popliteal artery BF was validated against conventional cine phase-contrast measures at rest and post-exercise recovery, while calf muscle energetics were validated by comparing to conventional 31P MRS-only measures at rest. To minimize motion artifacts during dynamic PFE, flow data were resolved in 3 dimensions (cardiac phase, pedal position, and exercise stage).
Results:
Resting phosphocreatine (PCr) and inorganic phosphate concentrations were similar between both techniques (both p > 0.05). During PFE, PCr declined to 46% ± 10% of rest. PCr recovery time was 43 ± 15 s. Resting BF was 132 ± 43 mL/min and increased up to four-fold during PFE depending on exercise stage and pedal position. Notably, there was excellent agreement between the interleaved and conventional BF measures (r2 = 0.95, slope = 0.977, p < 0.0001) with minimal bias (12.62 mL/min) over a wide range of physiologically relevant BF values (from ∼60 to 600 mL/min).
Conclusion:
The feasibility of simultaneous assessment of skeletal muscle energetics and BF during dynamic exercise by interleaved 31P MRS/1H flow MRI was demonstrated along with good agreement between interleaved and conventional techniques during rest and recovery. One can now simultaneously quantify critical BF-metabolism relationships and use this to probe disease-related adaptations.


