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Open AccessJournal ArticleDOI

The Trigeminovascular Pathway: Role of CGRP and CGRP Receptors in Migraine

Lars Edvinsson
- 01 May 2017 - 
- Vol. 57, pp 47-55
TLDR
There is still much to learn about the role of CGRP and C GRP receptors in headache pathophysiology, the critical anatomical sites, peripheral or central, of anti‐CGRP agents, and the potential involvement of CgrP‐related peptides and receptors.
Abstract
The trigeminal ganglion plays a key role in primary headache pathophysiology. Calcitonin gene-related peptide (CGRP) and CGRP receptors are expressed in trigeminal neurons that form C-fibers and A-fibers, respectively. In acute migraine and cluster headache attacks, there is release of CGRP into the cranial venous outflow. In addition, intravenous CGRP can induce migraine-like symptoms in migraine patients. These findings led to the development of anti-migraine therapies that inhibit CGRP action. Currently, CGRP receptor antagonists, the gepants, and monoclonal antibodies towards CGRP and the CGRP receptor are all showing positive relief of acute and chronic migraine in clinical trials. However, there is still much to learn about the role of CGRP and CGRP receptors in headache pathophysiology, the critical anatomical sites, peripheral or central, of anti-CGRP agents, and the potential involvement of CGRP-related peptides and receptors. This review provides a brief history of the discovery of the role of CGRP in migraine and highlights current progress in understanding the complexity of the trigeminovascular pathway and its peptide transmitters.

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Citations
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Journal ArticleDOI

CGRP as the target of new migraine therapies — successful translation from bench to clinic

TL;DR: Treatments that target calcitonin gene-related peptide (CGRP) and its receptor are proving effective for migraine treatment, and the hypothesis that CGRP has a major role in migraine pathophysiology is strongly supported.
Journal ArticleDOI

CGRP and the Trigeminal System in Migraine.

TL;DR: The goal of this narrative review is to provide an overview of migraine pathophysiology, with an emphasis on the role of calcitonin gene‐related peptide (CGRP) within the context of the trigeminovascular system.
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Does inflammation have a role in migraine

TL;DR: It is proposed that the increase in migraine frequency leading to chronic migraine involves neurogenic neuroinflammation, possibly entailing increased expression of cytokines via activation of protein kinases in neurons and glial cells of the trigeminovascular system.
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The Molecular Fingerprint of Dorsal Root and Trigeminal Ganglion Neurons

TL;DR: This work isolated lumbar DRG and TG neurons from Advillin-GFP transgenic mice and identified 24 genes which were uniquely expressed in either ganglia, giving each population a distinct molecular fingerprint.
References
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Journal ArticleDOI

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TL;DR: The approach described here permits the application of recombinant DNA technology to analyses of complex neurobiological systems in the absence of prior structural or biological information.
Journal ArticleDOI

Alternative RNA processing in calcitonin gene expression generates mRNAs encoding different polypeptide products

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Journal ArticleDOI

Vasoactive peptide release in the extracerebral circulation of humans during migraine headache

TL;DR: A substantial elevation of the calcitonin gene‐related peptide level in the external jugular but not the cubital fossa blood was seen in both classic and common migraine, and may have importance in the pathophysiology of migraine.
Journal ArticleDOI

Brain stem activation in spontaneous human migraine attacks.

TL;DR: Findings support the idea that the pathogenesis of migraine is related to an imbalance in activity between brain stem nuclei regulating antinociception and vascular control.
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