Cyclical changes of cortical excitability and metaplasticity in migraine: Evidence from a repetitive transcranial magnetic stimulation study

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• 作者：Giuseppe Cosentino ; ^{gcosentino80@gmail.com" class="auth_mail} ; Brigida Fierro ; Simone Vigneri ; Simona Talamanca ; Piera Paladino ; Roberta Baschi ; Serena Indovino ; Simona Maccora ; Francesca Valentino ; Enrico Fileccia ; Giuseppe Giglia ; Filippo Brighina
• 关键词：Magnetic stimulation ; Migraine with aura ; Migraine pathogenesis ; Headache ; Motor cortex ; Homeostatic plasticity
• 刊名：Pain
• 出版年：June 2014
• 年：2014
• 卷：155
• 期：6
• 页码：1070-1078
• 全文大小：1191 K

文摘

The primary brain dysfunctions leading to the onset of a migraine attack remain largely unknown. Other important open questions concern the mechanisms of initiation, continuation, and termination of migraine pain, and the changes in brain function underlying migraine transformation. Brief trains of high-frequency repetitive transcranial magnetic stimulation (rTMS), when applied to the primary motor cortex at suprathreshold intensity (猢?20% of resting motor threshold [RMT]), elicit in healthy subjects a progressive, glutamate-dependent facilitation of the motor evoked potentials (MEP). Conversely, in conditions of increased cortical excitability, the rTMS trains induce inhibitory MEP responses likely mediated by cortical homeostatic mechanisms. We enrolled 66 migraine-without-aura patients, 48 migraine-with-aura patients, 14 patients affected by chronic migraine (CM), and 20 healthy controls. We assessed motor cortical response to 5-Hz rTMS trains of 10 stimuli given at 120% RMT. Patients with episodic migraine were studied in different phases of the migraine cycle: interictal, preictal, ictal, and postictal states. Results showed a facilitatory MEP response during the trains in patients evaluated in the preictal phase, whereas inhibitory responses were observed during and after a migraine attack, as well as in CM patients. In the interictal phase, different responses were observed, depending on attack frequency: facilitation in patients with low and inhibition in those with high attack recurrence. Our findings suggest that changes in cortical excitability and fluctuations in the threshold for inhibitory metaplasticity underlie the migraine attack recurrence, and could be involved in the process of migraine transformation.