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October 26, 2010; 75 (17) Articles

Dilation by CGRP of middle meningeal artery and reversal by sumatriptan in normal volunteers

M.S. Asghar, A.E. Hansen, T. Kapijimpanga, R.J. van der Geest, P. van der Koning, H.B.W. Larsson, J. Olesen, M. Ashina
First published October 25, 2010, DOI: https://doi.org/10.1212/WNL.0b013e3181f9626a
M.S. Asghar
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A.E. Hansen
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T. Kapijimpanga
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R.J. van der Geest
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P. van der Koning
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H.B.W. Larsson
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J. Olesen
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Citation
Dilation by CGRP of middle meningeal artery and reversal by sumatriptan in normal volunteers
M.S. Asghar, A.E. Hansen, T. Kapijimpanga, R.J. van der Geest, P. van der Koning, H.B.W. Larsson, J. Olesen, M. Ashina
Neurology Oct 2010, 75 (17) 1520-1526; DOI: 10.1212/WNL.0b013e3181f9626a

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Abstract

Background: Calcitonin gene–related peptide (CGRP) plays a fundamental role in the pathophysiology of neurovascular headaches. CGRP infusion causes headache and dilation of cranial vessels. However, it is unknown to what extent CGRP-induced vasodilation contributes to immediate head pain and whether the migraine-specific abortive drug sumatriptan, a 5-hydroxytryptamine 1B/1D agonist, inhibits CGRP-induced immediate vasodilation and headache.

Methods: We performed a double-blind, randomized, placebo-controlled, crossover study in 18 healthy volunteers. We recorded circumference changes of the middle meningeal artery (MMA) and middle cerebral artery (MCA) using magnetic resonance angiography before and after infusion (20 minutes) of 1.5 μg/min human αCGRP or placebo (isotonic saline) as well as after a 6-mg sumatriptan subcutaneous injection.

Results: Compared with placebo, CGRP caused significant dilation of MMA (p = 0.006) and no dilation of MCA (p = 0.69). Sumatriptan caused a marked contraction of MMA (15%–25.2%) and marginal contraction of MCA (3.9% to 5.3%). Explorative analysis revealed that sumatriptan had a more selective action on MMA compared with MCA on the CGRP day (p < 0.0001) and on the placebo day (p = 0.007).

Conclusion: These data suggest that exogenous CGRP dilates extracranial vessels and not intracranial, and that sumatriptan exerts part of its antinociceptive action by constricting MMA and not MCA.

Classification of evidence: This study provides Class I evidence that IV GCRP causes dilation of the MMA but not the MCA in healthy volunteers, and that sumatriptan reverses the dilation of the MMA caused by CGRP.

Footnotes

  • Study funding: Supported by the University of Copenhagen, the Danish Headache Society, the Lundbeck Foundation through the Center for Neurovascular Signalling (LUCENS), the Danish Agency for Science, Technology and Innovation, and the Danish Council for Independent Research-Medical Sciences (FSS) (271-08-0446). This study is also supported by a research grant (no. 33936) from the Investigator Initiated Studies Program of Merck & Co., Inc. The opinions expressed in this article are those of the authors and do not necessarily represent those of Merck & Co., Inc.

  • AUC
    area under the curve
    BBB
    blood-brain barrier
    CBF
    cerebral blood flow
    CGRP
    calcitonin gene–related peptide
    CI
    confidence interval
    CO2
    carbon dioxide
    FOV
    field of view
    h-αCGRP
    human α-calcitonin gene–related peptide
    5-HT
    5-hydroxytryptamine
    MCA
    middle cerebral artery
    MMA
    middle meningeal artery
    MR
    magnetic resonance
    MRA
    magnetic resonance angiography
    pEC50
    negative logarithm of the EC50
    STA
    superficial temporal artery
    TE
    echo time
    TR
    repetition time
    VMCA
    blood velocity in middle cerebral artery
    VRS
    verbal rating scale

  • Editorial, page 1494

  • Supplemental data at www.neurology.org.

  • Received February 9, 2010.
  • Accepted June 14, 2010.
  • Copyright © 2010 by AAN Enterprises, Inc.
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