Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (65)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hoskin, K. L.
Right arrow Articles by Goadsby, P. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hoskin, K. L.
Right arrow Articles by Goadsby, P. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 119, No. 5, 1419-1428, 1996
© 1996 Guarantors of Brain


research-article

Sumatriptan can inhibit trigeminal afferents by an exclusively neural mechanism

Karen L. Hoskin1, Holger Kaube2 and Peter J. Goadsby1,

1Institute of Neurology, The National Hospital for Neurology and Neurosurgery London, UK 2Neurologische Klinik und Poliklinik, University of Essen Essen, Germany

Correspondence to: Dr Peter J. Goadsby, Institute of Neurology, Queen Square, London, WCIN 3BG, UK

SUMMMARY: Mechanical distortion of the human cranial venous sinuses is painful as is cranial venous sinus distension during migraine. Sumatriptan, the serotonin (5HT)IB/D-like receptor agonist, is highly effective in relieving migraine headache and part of its action may be due to constriction of cranial dural blood vessels. Using immunohistochemical detection of the immediate early gene Fos, we have mapped the spatial pattern of neural activation in the caudal medulla and the upper cervical spinal cord (C1, C2 and C3) in cats following either electrical or mechanical stimulation of the superior sagittal sinus. Fourteen cats were anaesthetized with {alpha}-chloralose and prepared for physiological monitoring of blood pressure, heart rate, rectal temperature and expired CO2. Electrical stimulation evoked significant increases in the (median) numbers of Fos-positive cells in laminae I and llo of the superficial dorsal horn of C1, C2 and C3 cervical spinal cord (88, 92 and 18 cells, respectively) and of the trigeminal nucleus caudalis (TNC) (81 cells). Mechanical stimulation revealed a similar pattern of neural activation but with reduced intensity in laminae I and IIo of the TNC (38 cells) and of C1 and C2 (32 and 31 cells, respectively). The temporalis muscle was stimulated mechanically in the control group and the numbers and distribution of Fos-positive cells were no different from those in non-stimulated controls. Treatment with sumatriptan reduced the numbers of Fos-positive cells found in laminae I and IIo of the TNC and C2 (6, 13 cells and 9 cells, respectively) after mechanical stimulation. These data suggest that the neural effect of sumatriptan alone is sufficient for significant attenuation of transmission in the trigeminal system. The fact that sumatriptan can inhibit trigeminal activation without its vascular effects suggests that drugs without a significant activity on blood vessels may be effective in the treatment of migraine.

migraine; headache; vascular pain; serotonin; cerebrovascular

Received February 9, 1996. Revised May 1, 1996. Accepted May 24, 1996.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
BrainHome page
G. G. Schoonman, J. van der Grond, C. Kortmann, R. J. van der Geest, G. M. Terwindt, and M. D. Ferrari
Migraine headache is not associated with cerebral or meningeal vasodilatation--a 3T magnetic resonance angiography study
Brain, August 1, 2008; 131(8): 2192 - 2200.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
R. Letienne, J.-C. Blanchet, E. Sole, G. W. John, and B. Le Grand
Donitriptan Decreases Jugular Venous Oxygen Saturation in Rats in the Absence of Cranial Vasoconstriction: An Overlooked Mechanism of Antimigraine Action?
J. Pharmacol. Exp. Ther., November 1, 2005; 315(2): 849 - 857.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
R. Letienne, Y. Verscheure, and G. W. John
Investigation of the Effects of Naratriptan, Rizatriptan, and Sumatriptan on Jugular Venous Oxygen Saturation in Anesthetized Pigs: Implications for Their Mechanism of Acute Antimigraine Action
J. Pharmacol. Exp. Ther., October 1, 2003; 307(1): 168 - 174.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
R. Letienne, Y. Verscheure, M. Perez, B. Le Grand, F. C. Colpaert, and G. W. John
Donitriptan Selectively Decreases Jugular Venous Oxygen Saturation in the Anesthetized Pig: Further Insights into Its Mechanism of Action Relevant to Headache Relief
J. Pharmacol. Exp. Ther., May 1, 2003; 305(2): 749 - 754.
[Abstract] [Full Text] [PDF]


Home page
CROBMHome page
B. J. Sessle
Acute and Chronic Craniofacial Pain: Brainstem Mechanisms of Nociceptive Transmission and Neuroplasticity, and Their Clinical Correlates
Critical Reviews in Oral Biology & Medicine, January 1, 2000; 11(1): 57 - 91.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
G. W. John, P. J. Pauwels, M. Perez, S. Halazy, B. Le Grand, Y. Verscheure, J.-P. Valentin, C. Palmier, T. Wurch, P. Chopin, et al.
F 11356, a Novel 5-Hydroxytryptamine (5-HT) Derivative with Potent, Selective, and Unique High Intrinsic Activity at 5-HT1B/1D Receptors in Models Relevant to Migraine
J. Pharmacol. Exp. Ther., July 1, 1999; 290(1): 83 - 95.
[Abstract] [Full Text]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.