Semi-Automated Recording of Facial Sensitivity in Rat Demonstrates Antinociceptive Effects of the Anti-CGRP Antibody Fremanezumab

Author:

Benedicter Nicola1,Messlinger Karl1ORCID,Vogler Birgit1,Mackenzie Kimberly D.2,Stratton Jennifer2,Friedrich Nadine3,Dux Mária3ORCID

Affiliation:

1. Institute of Physiology and Pathophysiology, Friedrich-Alexander-University, D-91054 Erlangen, Germany

2. Teva Pharmaceuticals, Redwood City, CA 94063, USA

3. Department of Physiology, University of Szeged, H-6720 Szeged, Hungary

Abstract

Migraine pain is frequently accompanied by cranial hyperalgesia and allodynia. Calcitonin gene-related peptide (CGRP) is implicated in migraine pathophysiology but its role in facial hypersensitivity is not entirely clear. In this study, we investigated if the anti-CGRP monoclonal antibody fremanezumab, which is therapeutically used in chronic and episodic migraines, can modify facial sensitivity recorded by a semi-automatic system. Rats of both sexes primed to drink from a sweet source had to pass a noxious mechanical or heat barrier to reach the source. Under these experimental conditions, animals of all groups tended to drink longer and more when they had received a subcutaneous injection of 30 mg/kg fremanezumab compared to control animals injected with an isotype control antibody 12–13 days prior to testing, but this was significant only for females. In conclusion, anti-CGRP antibody, fremanezumab, reduces facial sensitivity to noxious mechanical and thermal stimulation for more than one week, especially in female rats. Anti-CGRP antibodies may reduce not only headache but also cranial sensitivity in migraineurs.

Funder

Hungarian National Research, Development and Innovation Office

Alexander von Humboldt Foundation

Teva

Friedrich-Alexander-Universität Erlangen-Nürnberg

Publisher

MDPI AG

Subject

Neurology (clinical)

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