Artigo Revisado por pares

Sumatriptan normalizes the migraine attack-related increase in brain serotonin synthesis

2008; Lippincott Williams & Wilkins; Volume: 70; Issue: 6 Linguagem: Inglês

10.1212/01.wnl.0000299095.65331.6f

ISSN

1526-632X

Autores

Yusuke Sakai, CF Dobson, Mirko Dikšić, M Aubé, Édith Hamel,

Tópico(s)

Sympathectomy and Hyperhidrosis Treatments

Resumo

Altered serotonin (5-HT) neurotransmission has been implicated in the pathophysiology of migraine headache.To test this hypothesis in migraine patients in vivo using PET and alpha-[(11)C]methyl-l-tryptophan as a surrogate marker of brain 5-HT synthetic rate during different phases of their migraine attack and after acute antimigraine therapy with sumatriptan, and to compare them with normal controls.Six patients were scanned 1) within 6 hours after the onset of a spontaneous migraine attack, 2) 2 hours after subcutaneous sumatriptan, and 3) interictally when migraine free for at least 3 days. Head pain was rated before each scan, and before and every 15 minutes after sumatriptan.Brain 5-HT synthesis was highest during attacks, lowest after sumatriptan, and intermediate when patients were migraine free. All states were statistically different from the others in virtually all brain regions examined. 5-HT synthetic rates in patients during migraine attacks did not differ from those of age- and sex-matched controls, whereas they were significantly lower after sumatriptan in a majority of regions. Interictally, global brain 5-HT synthetic rate was slightly, albeit not significantly, lower (-14%) in migraine patients than in controls, with specific cortical areas exhibiting proportionally more severe reductions (-28% to 31%).These findings point to a low cortical serotonergic tone in migraine patients interictally. Further, they demonstrate widespread increases in brain serotonin (5-HT) synthetic rate in migraine patients during attacks, and that triptans exert a negative feedback regulation of brain 5-HT synthesis concurrently with modulation of pain pathways.

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