Fronto-insular circuit mechanisms of accelerated intermittent theta burst stimulation
Summary
Transcranial magnetic stimulation (TMS) is a widely used neuromodulation treatment for depression, but its mechanisms are poorly understood. Indirect clinical evidence suggests that TMS enhances plasticity within the prefrontal cortical target site and engages downstream networks. However, establishing causal mechanisms to help optimize the large stimulation parameter space has been challenging. Using an optogenetic model of accelerated intermittent theta burst stimulation (prelimbic PL-ai
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# Fronto-insular circuit mechanisms of accelerated intermittent theta burst stimulation
*Published: 2026 May 14*
Transcranial magnetic stimulation (TMS) is a widely used neuromodulation
treatment for depression, but its mechanisms are poorly understood. Indirect
clinical evidence suggests that TMS enhances plasticity within the prefrontal
cortical target site and engages downstream networks. However, establishing
causal mechanisms to help optimize the large stimulation parameter space has
been challenging. Using an optogenetic model of accelerated intermittent theta
burst stimulation (prelimbic [PL]-aiTBS) that drives rapid antidepressant-like
effects, we examined cell type-specific effects on synapse-related gene
expression, increased spine density, and increased excitatory currents in
prefrontal intratelencephalic projection neurons. Whole-brain c-Fos
immunolabeling, fiber photometry, chemogenetic, and projection-specific
optogenetic manipulations revealed that PL-aiTBS activates a fronto-insular
network that is necessary and sufficient for its antidepressant-like behavioral
effects. Finally, we validate a key role for fronto-insular connectivity and
TMS-evoked responses in the human insula using intracortical
stereo-electroencephalogram (EEG) and resting-state fMRI. These results
establish a fronto-insular circuit as a critical mediator of the antidepressant
effects of aiTBS.
DOI: 10.1016/j.cell.2026.04.030