Left dorsolateral prefrontal cortex activation can accelerate stress recovery: A repetitive transcranial stimulation study

In this study, a single high-frequency repetitive transcranial magnetic stimulation (HF-rTMS) session was applied over the left dorsolateral prefrontal cortex (DLPFC) after a moderate-to-intense stressor to investigate whether left DLPFC stimulation could regulate cortisol concentration after stress induction. Participants were randomly divided into three groups (stress-TMS, stress, and placebo-stress). Stress was induced in both the stress-TMS and stress groups using the Trier Social Stress Test (TSST). The placebo-stress group received a placebo TSST. In the stress-TMS group, a single HF-rTMS session was applied over the left DLPFC after TSST. Cortisol was measured across the different groups, and each group's responses to the stress-related questionnaire were recorded. After TSST, both the stress-TMS and stress groups reported increased self-reported stress, state anxiety, negative affect, and cortisol concentration compared with the placebo-stress group, indicating that TSST successfully induced a stress response. Compared with the stress group, the stress-TMS group exhibited reduced cortisol levels at 0, 15, 30, and 45 min after HF-rTMS. These results suggest that left DLPFC stimulation after stress induction might accelerate the stress recovery.

Automated summary

This study investigated the effects of high-frequency repetitive transcranial magnetic stimulation (HF-rTMS) over the left dorsolateral prefrontal cortex (DLPFC) on cortisol concentration after stress induction. Participants were randomly assigned to stress-TMS, stress, and placebo-stress groups. Stress was induced using the Trier Social Stress Test (TSST), and the stress-TMS group received HF-rTMS after TSST. Cortisol levels and stress-related responses were measured. The stress-TMS group showed reduced cortisol levels compared with the stress group, indicating that left DLPFC stimulation after stress induction may promote stress recovery.