Differential effect of low and high frequency transcranial magnetic stimulation on cortical excitability and myelination after neonatal hypoxia in mice.

Premature infants are highly susceptible to intermittent hypoxic brain injury, which is associated with adverse motor, cognitive, and behavioral outcomes, including deficits in attention, hyperactivity, and learning. Previous animal studies have shown myelination deficits and increased glutamatergic synaptic strength in the sensory-motor cortex. The study investigates the feasibility, safety, and therapeutic potential of repetitive transcranial magnetic stimulation (rTMS) in ameliorating central hypomyelination, reducing excessive glutamatergic transmission in cortical neurons following neonatal intermittent hypoxia (IH), and improving behavioral outcomes. In the mouse model of neonatal intermittent hypoxia, low-frequency (LF-rTMS) stimulation at 1 Hz or high-frequency (HF-rTMS) at 10 Hz stimulation was applied for 5 days shortly after the IH injury. The rTMS regimen did not induce apoptosis or inflammation. HF-rTMS significantly ameliorated hypomyelination in the corticospinal tract, with a larger increase in MPF in the stimulated hemisphere and also in the contralateral hemisphere. LF-rTMS reduced locomotor hyperactivity in female IH mice and decreased elevated glutamatergic synaptic excitability in motor cortex slices. This study provides evidence that rTMS can modulate both myelination and synaptic excitability, leading to improved behavioral outcomes after neonatal hypoxic brain injury. These findings highlight the therapeutic potential of rTMS as an early intervention strategy for neurological sequelae of perinatal hypoxia.