Second messenger signalling bypasses CGRP receptor blockade to provoke migraine attacks in humans

There are several endogenous molecules that can trigger migraine attacks when administered to humans. Notably, calcitonin gene-related peptide (CGRP) has been identified as a key player in a signalling cascade involved in migraine attacks, acting through the second messenger cyclic adenosine monophosphate (cAMP) in various cells, including intracranial vascular smooth muscle cells. However, it remains unclear whether intracellular cAMP signalling requires CGRP receptor activation during a migraine attack in humans. To address this question, we conducted a randomized, double-blind, placebo-controlled, parallel trial using a human provocation model involving the administration of CGRP and cilostazol in individuals with migraine pretreated with erenumab or placebo. Our study revealed that migraine attacks can be provoked in patients by cAMP-mediated mechanisms using cilostazol, even when the CGRP receptor is blocked by erenumab. Furthermore, the dilation of cranial arteries induced by cilostazol was not influenced by the CGRP receptor blockade. These findings provide clinical evidence that cAMP-evoked migraine attacks do not require CGRP receptor activation. This discovery opens up new possibilities for the development of mechanism-based drugs for the treatment of migraine. Using a human migraine provocation model, Do et al. provide clinical evidence that cAMP-evoked migraine attacks do not require CGRP receptor activation. These findings open up new avenues for mechanism-based drug development for migraine.

Automated summary

This study found that migraine attacks can be triggered by cAMP-mediated mechanisms without the activation of CGRP receptors. This opens up new possibilities for the development of mechanism-based drugs for the treatment of migraines.