Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.

Journal Article (Journal Article)

Familial hemiplegic migraine type 1, a monogenic migraine variant with aura, is linked to gain-of-function mutations in the CACNA1A gene encoding Ca(V)2.1 channels. The S218L mutation causes severe channel dysfunction, and paroxysmal migraine attacks can be accompanied by seizures, coma, and hemiplegia; patients expressing the R192Q mutation exhibit hemiplegia only. Familial hemiplegic migraine knock-in mice expressing the S218L or R192Q mutation are highly susceptible to cortical spreading depression, the electrophysiological surrogate for migraine aura, and develop severe and prolonged motor deficits after spreading depression. The S218L mutants also develop coma and seizures and sometimes die. To investigate underlying mechanisms for these symptoms, we used multielectrode electrophysiological recordings, diffusion-weighted magnetic resonance imaging, and c-fos immunohistochemistry to trace spreading depression propagation into subcortical structures. We showed that unlike the wild type, cortical spreading depression readily propagated into subcortical structures in both familial hemiplegic migraine type 1 mutants. Whereas the facilitated subcortical spread appeared limited to the striatum in R192Q, hippocampal and thalamic spread was detected in the S218L mutants with an allele-dosage effect. Both strains exhibited increased susceptibility to subcortical spreading depression and reverberating spreading depression waves. Altogether, these data show that spreading depression propagates between cortex, basal ganglia, diencephalon, and hippocampus in genetically susceptible brains, which could explain the prolonged hemiplegia, coma, and seizure phenotype in this variant of migraine with aura.

Full Text

Duke Authors

Cited Authors

  • Eikermann-Haerter, K; Yuzawa, I; Qin, T; Wang, Y; Baek, K; Kim, YR; Hoffmann, U; Dilekoz, E; Waeber, C; Ferrari, MD; van den Maagdenberg, AMJM; Moskowitz, MA; Ayata, C

Published Date

  • April 13, 2011

Published In

Volume / Issue

  • 31 / 15

Start / End Page

  • 5755 - 5763

PubMed ID

  • 21490217

Pubmed Central ID

  • PMC3135337

Electronic International Standard Serial Number (EISSN)

  • 1529-2401

Digital Object Identifier (DOI)

  • 10.1523/JNEUROSCI.5346-10.2011


  • eng

Conference Location

  • United States