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Cortical spreading depression as a site of origin for migraine: Role of CGRP

  • Liesl N. Close
  • , Sajedeh Eftekhari
  • , Minyan Wang
  • , Andrew C. Charles
  • , Andrew F. Russo*
  • *Corresponding author for this work
  • University of Iowa
  • University of California at Los Angeles
  • Department of Veterans Affairs

Research output: Contribution to journalReview articlepeer-review

111 Citations (Scopus)

Abstract

Premise: Migraine is a complex neurologic disorder that leads to significant disability, yet remains poorly understood. Problem: One potential triggering mechanism in migraine with aura is cortical spreading depression, which can activate the trigeminal nociceptive system both peripherally and centrally in animal models. A primary neuropeptide of the trigeminal system is calcitonin gene-related peptide, which is a potent vasodilatory peptide and is currently a major therapeutic target for migraine treatment. Despite the importance of both cortical spreading depression and calcitonin gene-related peptide in migraine, the relationship between these two players has been relatively unexplored. However, recent data suggest several potential vascular and neural connections between calcitonin gene-related peptide and cortical spreading depression. Conclusion: This review will outline calcitonin gene-related peptide-cortical spreading depression connections and propose a model in which cortical spreading depression and calcitonin gene-related peptide act at the intersection of the vasculature and cortical neurons, and thus contribute to migraine pathophysiology.

Original languageEnglish
Pages (from-to)428-434
Number of pages7
JournalCephalalgia
Volume39
Issue number3
DOIs
Publication statusPublished - Mar 2019

Keywords

  • cortical spreading depression
  • Neurovasculature
  • trigeminal nerve
  • vasodilation

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