MOTOR CORTEX TDCS SELECTIVELY INHIBITS TRIGEMINOCERVICAL COMPLEX NEURONS IN A SEX- AND HORMONE-DEPENDENT MANNER
Inserm U1107 - Université Clermont Auvergne
Presentation
Date TBA
Event Information
Poster Board
PS01-07AM-453
Poster
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Using a rodent model, electrodes were implanted over the motor M1 and occipital cortex of anesthetized male, cycling female, and ovariectomized (OVX) rats. A single tDCS session (200 µA-20 min) was applied. We conducted unitary extracellular recordings of TCC neurons to evaluate responses to nociceptive stimuli and performed immunohistochemical analysis of phosphorylated ERK (p-ERK) expression.
Our findings demonstrate that M1-tDCS induces a robust inhibition of TCC neuron activity in response to electrical C-fiber stimulation in both males and cycling females but not in OVX females. Furthermore, tDCS efficacy was significantly more pronounced in females during the Proestrus/Estrus phases compared to the Metestrus/Diestrus, suggesting that sexual hormones act as critical facilitators of the neuromodulatory response.
Immunohistochemical analysis also revealed that a single tDCS session triggers a bilateral overexpression of p-ERK within the TCC. Notably, significant microglial activation (p-ERK+/Iba1+) was observed in cycling and OVX females but was absent in males.
These findings demonstrate that tDCS efficacy is dictated by sex and hormonal status. The absence of a microglial signature in males, despite clear electrophysiological inhibition, reveals a profound sexual dimorphism in the neuromodulatory circuits recruited by tDCS.
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