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Elucidating the nociceptive role of CGRP in migraine headache

Title: Elucidating the nociceptive role of CGRP in migraine headache
Authors: Melo-Carrillo, Agustin; Strassman, Andrew; Burstein, Rami
Source: Brain ; ISSN 0006-8950 1460-2156
Publisher Information: Oxford University Press (OUP)
Publication Year: 2026
Description: Calcitonin gene-related peptide (CGRP) is thought to be a key player in the pathogenesis of migraine, but there is a fundamental mystery in that the known neuronal actions of CGRP do not account for how it causes pain. We now report the first finding of CGRP-induced nociceptive neuronal activation using a novel method of intra-carotid infusion to achieve a more targeted delivery to cranial tissues. Single-unit recordings were performed in anesthetized rats to measure CGRP effects on first- and second-order trigeminovascular neurons. CGRP was administered via intra-carotid infusion. Neuronal activation and sensitization were assessed by spontaneous firing rates and responses to mechanical stimulation of dural and facial receptive fields. Lidocaine was applied locally to the dura or trigeminal ganglion at varying time points to determine the peripheral contribution to CGRP-induced activity. Intra-carotid CGRP infusion (5 µg/kg/min, 20 min) activated 62% of Aδ-fibers and 56% of C-fibers, with significant increases in firing rates beginning within the first 30 minutes for Aδ-fibers and after one hour for C-fibers. It also activated 75% of central trigeminovascular neurons, significantly increasing spontaneous firing and sensitizing dural and facial receptive fields. Similar effects were produced by CGRP injection into the trigeminal ganglion. These effects of CGRP were impeded by local anesthetic blockade of the dura or trigeminal ganglion before but not 1 hour after CGRP infusion. No significant sex differences were found in baseline firing or in the magnitude and timing of CGRP-induced responses across all neuron types. These finding provide the first evidence of peripheral nociceptive neuronal activation by CGRP, with a site of action in the meninges, and support a rationale for early, peripherally acting CGRP-targeted migraine treatments.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/brain/awag008
DOI: 10.1093/brain/awag008/66302028/awag008.pdf
Availability: https://doi.org/10.1093/brain/awag008; https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awag008/66302028/awag008.pdf
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.4ED28F28
Database: BASE