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Neurology 1999;53:2069
© 1999 American Academy of Neurology


Articles

Menstrual cycle effects on cortical excitability

M. J. Smith, MD, PhD, J. C. Keel, BA, B. D. Greenberg, MD, PhD, L. F. Adams, BA, P. J. Schmidt, MD, D. A. Rubinow, MD and E. M. Wassermann, MD

From the National Institute of Mental Health (Drs. Smith, Greenberg, Schmidt, and Rubinow, and J.C. Keel and L.F. Adams) and National Institute of Neurological Disorders and Stroke (Dr. Wassermann), National Institutes of Health, Bethesda, MD.

Address correspondence and reprint requests to Dr. Eric M. Wassermann, National Institute of Neurological Disorders and Stroke, 10 Center Drive, MSC 1428, Bethesda, MD 20892-1428.

OBJECTIVE: To determine whether there are menstrual cycle–related effects on cortical excitability in normal women.

BACKGROUND: Ovarian steroid hormones affect neurotransmission in the brain. Data from animal experiments have shown that progesterone metabolites enhance the action of gamma-aminobutyric acid (GABA), the main inhibitory neurotransmitter in the cortex, producing benzodiazepine-like (e.g., diazepam and lorazepam) physiologic and behavioral effects. Estradiol has excitatory effects on measures of neuronal excitability, possibly acting through the glutamate system. These effects have been difficult to detect in women using conventional techniques. However, recently, paired transcranial magnetic stimulation (TMS) has been used to detect the effects of GABAergic and glutamatergic drugs in humans. We used this method to measure the effects of the menstrual cycle in normal women.

METHODS: We tested 13 healthy women during the follicular (low-progesterone) and luteal (high-progesterone) phases of the menstrual cycle using paired TMS. The effect of a subthreshold conditioning pulse on the cortex was tested by measuring the response to a second suprathreshold test pulse and comparing it with the response elicited by the test pulse administered alone.

RESULTS: Conditioning TMS produced more inhibition in the luteal phase than in the follicular phase (p = 0.01), of similar magnitude to the reported effect of benzodiazepine drugs.

CONCLUSIONS: This study provides the first direct evidence of changes in the excitability of a cortical network with the menstrual cycle. The results also show a potential confound for studies using transcranial magnetic stimulation in populations that include menstruating women.

Key words: Motor cortex—Menstrual cycle—Magnetic stimulation—Paired stimulation—Neurosteroids—Gamma-aminobutyric acid receptors—Progesterone.




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