Resonancia Magnética Funcional de Sodio (NARS) Relacionada con la Actividad Neuronal Revela Dinámicas Neuronales de Milisegundos Más Allá de las Lecturas Hemodinámicas

Brain-wide, noninvasive methods that directly resolve neuronal activity on millisecond timescales are still lacking in neuroimaging. Hemodynamic fMRI ( ¹ H-based) provides whole-brain maps of activity, yet its vascular origin creates spatial and temporal displacements from neuronal events that complicate interpretation, especially in disease conditions where neurovascular coupling is altered. Here, we developed an ultrafast ²³ Na fMRI platform at 14 T that combines a reshuffled k-t 3D gradient echo readout (TR/TE, 10ms/1ms) with an implantable RF coil and respiration-gated acquisition. This configuration provides the sampling rate and SNR needed to probe quadrupolar T2*-weighted single quantum sodium dynamics on the neuronal timescale. Across rats and mice, somatosensory forepaw stimulation produced a localized ²³ Na signal decrease of ~2-3% in the FP-S1, peaking ~10-30 ms post-stimulus. The activity pattern is well matched with conventional BOLD-fMRI maps acquired in the same animals. Trial-by-trial measurements during simultaneous iGluSnFR glutamate fiber photometry demonstrated that larger evoked glutamate transients coincided with larger NARS decreases, supporting a neuronal origin of the NARS contrast. We interpret the negative NARS response as a transient activity-dependent redistribution of sodium ions toward restricted, protein-rich microdomains, where more restricted rotational dynamics may accelerate T2*short decay and produce a 2-3% signal decrease without requiring large changes in bulk sodium concentration. Together, these results establish neural activity-related sodium (NARS) fMRI as a viable approach for direct, mesoscale neuronal mapping with MRI at millisecond resolution.

Yu et al. introduce NARS-fMRI, an ultrafast ²³ Na method that resolves millisecond neuronal dynamics in rodent FP-S1. The negative sodium response (10-30 ms) co-localizes with BOLD and correlates with glutamate photometry, supporting a direct neuronal origin.