Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice

Ann Neurol. 2009 Oct;66(4):564-8. doi: 10.1002/ana.21779.

Abstract

Familial hemiplegic migraine type 1 (FHM1), a severe migraine with aura variant, is caused by mutations in the CACNA1A gene. Mutant mice carrying the FHM1 R192Q mutation exhibit increased propensity for cortical spreading depression (CSD), a propagating wave of neuroglial depolarization implicated in migraine aura. The CSD phenotype is stronger in female R192Q mutants and diminishes after ovariectomy. Here, we show that orchiectomy reciprocally increases CSD susceptibility in R192Q mutant mice. Chronic testosterone replacement restores CSD susceptibility by an androgen receptor-dependent mechanism. Hence, androgens modulate genetically-enhanced CSD susceptibility and may provide a novel prophylactic target for migraine.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium Channels / deficiency
  • Calcium Channels / genetics
  • Cortical Spreading Depression / genetics*
  • Gene Knock-In Techniques*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Migraine with Aura / genetics*
  • Migraine with Aura / metabolism*
  • Orchiectomy
  • Point Mutation*
  • Testosterone / genetics*
  • Testosterone / physiology

Substances

  • CACNA1A protein, human
  • Calcium Channels
  • Testosterone