The influence of menstrual phase on synaptic plasticity induced via intermittent theta-burst stimulation

•Biological females display a variable propensity for plasticity via rTMS that reflects the phase of the menstrual cycle.•Synaptic plasticity induced by iTBS occurs during the follicular and not luteal phase.•SICI is unchanged following iTBS. Ovarian hormones influence the propensity for short-term...

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Veröffentlicht in:Neuroscience 2024-10, Vol.558, p.122-127
Hauptverfasser: Ramdeo, K.R., Adams, F.C., Drapeau, C.C., Foglia, S.D., Cuizon, M.C., Sader, M.A., Nucci, R., Nelson, A.J.
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Sprache:eng
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Zusammenfassung:•Biological females display a variable propensity for plasticity via rTMS that reflects the phase of the menstrual cycle.•Synaptic plasticity induced by iTBS occurs during the follicular and not luteal phase.•SICI is unchanged following iTBS. Ovarian hormones influence the propensity for short-term plasticity induced by repetitive transcranial magnetic stimulation (rTMS). Estradiol appears to enhance the propensity for neural plasticity. It is currently unknown how progesterone influences short-term plasticity induced by rTMS. The present research investigates whether the luteal versus follicular phase of the menstrual cycle influence short-term plasticity induced by intermittent theta-burst stimulation (iTBS). We tested the hypothesis that iTBS would increase motor evoked potentials (MEPs) during the follicular phase. Further, we explored the effects of the luteal phase on iTBS-induced neural plasticity. Twenty-nine adult females participated in a placebo-controlled study that delivered real and sham iTBS to the left primary motor cortex in separate sessions corresponding to the follicular phase (real iTBS), luteal phase (real iTBS), and a randomly selected day (sham iTBS). Outcomes included corticospinal excitability as measured by the amplitude of MEPs and short-interval intracortical inhibition (SICI) recorded from the right first dorsal interosseous muscle before and following iTBS (612 pulses). MEP amplitude was increased following real iTBS during the follicular condition. No significant changes in MEP amplitude were observed during the luteal or sham visits. SICI was unchanged by iTBS irrespective of menstrual phase. These findings suggest women experience a variable propensity for iTBS-induced short-term plasticity across the menstrual cycle. This information is important for designing studies aiming to induce plasticity via rTMS in women.
ISSN:0306-4522
1873-7544
1873-7544
DOI:10.1016/j.neuroscience.2024.08.023