Female-selective mechanisms promoting migraine.


Journal

The journal of headache and pain
ISSN: 1129-2377
Titre abrégé: J Headache Pain
Pays: England
ID NLM: 100940562

Informations de publication

Date de publication:
24 Apr 2024
Historique:
received: 03 04 2024
accepted: 15 04 2024
medline: 25 4 2024
pubmed: 25 4 2024
entrez: 24 4 2024
Statut: epublish

Résumé

Sexual dimorphism has been revealed for many neurological disorders including chronic pain. Prelicinal studies and post-mortem analyses from male and female human donors reveal sexual dimorphism of nociceptors at transcript, protein and functional levels suggesting different mechanisms that may promote pain in men and women. Migraine is a common female-prevalent neurological disorder that is characterized by painful and debilitating headache. Prolactin is a neurohormone that circulates at higher levels in females and that has been implicated clinically in migraine. Prolactin sensitizes sensory neurons from female mice, non-human primates and humans revealing a female-selective pain mechanism that is conserved evolutionarily and likely translationally relevant. Prolactin produces female-selective migraine-like pain behaviors in rodents and enhances the release of calcitonin gene-related peptide (CGRP), a neurotransmitter that is causal in promoting migraine in many patients. CGRP, like prolactin, produces female-selective migraine-like pain behaviors. Consistent with these observations, publicly available clinical data indicate that small molecule CGRP-receptor antagonists are preferentially effective in treatment of acute migraine therapy in women. Collectively, these observations support the conclusion of qualitative sex differences promoting migraine pain providing the opportunity to tailor therapies based on patient sex for improved outcomes. Additionally, patient sex should be considered in design of clinical trials for migraine as well as for pain and reassessment of past trials may be warranted.

Identifiants

pubmed: 38658853
doi: 10.1186/s10194-024-01771-w
pii: 10.1186/s10194-024-01771-w
doi:

Substances chimiques

Calcitonin Gene-Related Peptide JHB2QIZ69Z
Prolactin 9002-62-4

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

63

Subventions

Organisme : National Institute for Health Care Management Foundation
ID : R01NS1295
Organisme : National Institute for Health Care Management Foundation
ID : R01NS1295

Informations de copyright

© 2024. The Author(s).

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Auteurs

Shagun Singh (S)

Banner - University Medicine Sunrise Primary Care, Tucson, AZ, 85750, USA.

Caroline M Kopruszinski (CM)

Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, 85724, USA.

Moe Watanabe (M)

Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, 85724, USA.

David W Dodick (DW)

Department of Neurology, Mayo Clinic, Phoenix, AZ, USA.
Atria Academy of Science and Medicine, New York, NY, USA.

Edita Navratilova (E)

Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, 85724, USA.
Department of Neurology, Mayo Clinic, Phoenix, AZ, USA.

Frank Porreca (F)

Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, 85724, USA. frankp@arizona.edu.
Department of Neurology, Mayo Clinic, Phoenix, AZ, USA. frankp@arizona.edu.

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