Chronification of migraine sensitizes to CGRP in male and female mice
As previously reported, CGRP produced female-selective migraine-like pain behaviors in naïve mice. Consistent with behavioral effects, female mice demonstrated a higher number of CGRP-positive cells in the TGV1. These findings appear relevant to clinical observations of female efficacy of CGRP-receptor antagonists for acute treatment in EM patients. In models of CM or MOH that are characterized by increased frequency of migraine-like pain, previously subthreshold doses of supradural CGRP now elicited migraine-like nociceptive behaviors in mice of both sexes. The increased pain responses were accompanied by increased number CGRP positive TGV1 cells in the NTG model in both female and male mice. These data suggest that increased frequency of migraine promotes physiological changes including increased expression of TGV1 CGRP along with sensitization to CGRP-induced nociception in both males and females. Thus, as EM transforms to CM, CGRP-dependent mechanisms may become increasingly important, consistent with observations of efficacy of CGRP targeting therapies for migraine prevention in both men and women. Our results also suggest the possibility of enhanced efficacy of CGRP-receptor antagonists for the acute treatment of migraine in men as migraine frequency increases.
Authors
- Robson Cristiano Lillo Vizin (ORCID: https://orcid.org/0000-0003-2021-5474)
- Kara R. Barber (ORCID: https://orcid.org/0000-0002-4042-9886)
- David W. Dodick (ORCID: https://orcid.org/0000-0002-9486-6790)
- Edita Navratilova (ORCID: https://orcid.org/0000-0002-1497-125X)
- Frank Porreca (ORCID: https://orcid.org/0000-0002-2267-0617)
- Germán Guzmán
- Caroline Machado Kopruszinski (ORCID: https://orcid.org/0000-0002-5392-5117)
Institutions
- University of Arizona (US)
- Mayo Clinic Hospital (US)
Publication Details
- Journal
- Cephalalgia
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1177/03331024251317446
- Citations
- 9
- Primary Topic
- Migraine and Headache Studies
- Type
- article
- Field-Weighted Citation Impact
- 13.24
Funders
- National Institutes of Health