What question did this study set out to answer?

The aim is to examine the dynamics of lactate clearance and T2 relaxation in human skeletal muscle using a new 1H MRS technique.

February 12, 2026Open Access

Postexercise Lactate Clearance, T 2 Relaxation, and J ‐Modulation in Human Skeletal Muscle Measured With Double‐Quantum Filtered 1 H MRS at 7 T

Puntos clave

The aim is to examine the dynamics of lactate clearance and T2 relaxation in human skeletal muscle using a new 1H MRS technique.
Used a two-channel 1H transceiver coil at 7 T for localized measurements.
Applied a CH-selective double quantum filter (DQF) sequence to measure postexercise calf muscle in 11 subjects.
Interleaved constant and incrementing TE measurements to assess lactate decrease and T2.
DQF improved lactate detection, yielding clear signals in 4-second measurements.
Lactate clearance half-time was 162 ± 42 s; T2 relaxation time was 138 ± 20 ms.
The new CH-selective sequence provided up to 2.3 times higher signal compared to traditional methods.

Resumen

ABSTRACT Purpose 1 H MRS lactate measurements are potentially valuable for studying energy metabolism in working skeletal muscle, but some technical obstacles need to be overcome. Spectral filtering to isolate the lactate signal from overlapping lipid resonances shows promise. We report a novel sequence with 3D localisation and a CH‐selective double quantum filter (DQF) which enables dynamic postexercise single‐shot measurement of cellular lactate T 2 and clearance kinetics. Methods Using a two‐channel 1 H transceiver coil at 7 T we applied a localized CH‐selective DQF sequence to postexercise calf muscle in 11 subjects. In one leg acquisitions with constant and incrementing T E were interleaved to measure lactate decrease and T 2 . In the other the CH‐selective sequence was interleaved with the nonselective variant. Results Postexercise DQF shows lactate clearly in 4 s single‐shot spectra. Fitting was able to separate lactate concentration kinetics from T 2 and J ‐modulation: clearance t 1/2 = 162 ± 42 s and T 2 = 138 ± 20 ms (mean ± SD); the scalar coupling constant fitted from time evolution was J = 16.6 ± 0.8 Hz, closely matching J = 16.5 ± 1.3 Hz derived from spectral splitting. Direct comparison showed 2.3 ± 0.9 times higher signal with the new CH‐selective sequence. Conclusions The new sequence improved lactate detection, enabling quantification from single shots postexercise with time resolution similar to 31 P MRS. Measuring clearance and relaxation time constants of intramuscular lactate lays the groundwork for future absolute quantification and studies of intra‐ and extracellular lactate compartmentation based on dipolar coupling differences.

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