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Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients

BACKGROUND: The brainstem contains descending circuitry that can modulate nociceptive processing (neural signals associated with pain) in the dorsal horn of the spinal cord and the medullary dorsal horn. In migraineurs, abnormal brainstem function during attacks suggest that dysfunction of descendin...

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Autores principales: Moulton, Eric A., Burstein, Rami, Tully, Shannon, Hargreaves, Richard, Becerra, Lino, Borsook, David
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582961/
https://www.ncbi.nlm.nih.gov/pubmed/19030105
http://dx.doi.org/10.1371/journal.pone.0003799
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author Moulton, Eric A.
Burstein, Rami
Tully, Shannon
Hargreaves, Richard
Becerra, Lino
Borsook, David
author_facet Moulton, Eric A.
Burstein, Rami
Tully, Shannon
Hargreaves, Richard
Becerra, Lino
Borsook, David
author_sort Moulton, Eric A.
collection PubMed
description BACKGROUND: The brainstem contains descending circuitry that can modulate nociceptive processing (neural signals associated with pain) in the dorsal horn of the spinal cord and the medullary dorsal horn. In migraineurs, abnormal brainstem function during attacks suggest that dysfunction of descending modulation may facilitate migraine attacks, either by reducing descending inhibition or increasing facilitation. To determine whether a brainstem dysfunction could play a role in facilitating migraine attacks, we measured brainstem function in migraineurs when they were not having an attack (i.e. the interictal phase). METHODS AND FINDINGS: Using fMRI (functional magnetic resonance imaging), we mapped brainstem activity to heat stimuli in 12 episodic migraine patients during the interictal phase. Separate scans were collected to measure responses to 41°C and noxious heat (pain threshold+1°C). Stimuli were either applied to the forehead on the affected side (as reported during an attack) or the dorsum of the hand. This was repeated in 12 age-gender-matched control subjects, and the side tested corresponded to that in the matched migraine patients. Nucleus cuneiformis (NCF), a component of brainstem pain modulatory circuits, appears to be hypofunctional in migraineurs. 3 out of the 4 thermal stimulus conditions showed significantly greater NCF activation in control subjects than the migraine patients. CONCLUSIONS: Altered descending modulation has been postulated to contribute to migraine, leading to loss of inhibition or enhanced facilitation resulting in hyperexcitability of trigeminovascular neurons. NCF function could potentially serve as a diagnostic measure in migraine patients, even when not experiencing an attack. This has important implications for the evaluation of therapies for migraine.
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spelling pubmed-25829612008-11-24 Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients Moulton, Eric A. Burstein, Rami Tully, Shannon Hargreaves, Richard Becerra, Lino Borsook, David PLoS One Research Article BACKGROUND: The brainstem contains descending circuitry that can modulate nociceptive processing (neural signals associated with pain) in the dorsal horn of the spinal cord and the medullary dorsal horn. In migraineurs, abnormal brainstem function during attacks suggest that dysfunction of descending modulation may facilitate migraine attacks, either by reducing descending inhibition or increasing facilitation. To determine whether a brainstem dysfunction could play a role in facilitating migraine attacks, we measured brainstem function in migraineurs when they were not having an attack (i.e. the interictal phase). METHODS AND FINDINGS: Using fMRI (functional magnetic resonance imaging), we mapped brainstem activity to heat stimuli in 12 episodic migraine patients during the interictal phase. Separate scans were collected to measure responses to 41°C and noxious heat (pain threshold+1°C). Stimuli were either applied to the forehead on the affected side (as reported during an attack) or the dorsum of the hand. This was repeated in 12 age-gender-matched control subjects, and the side tested corresponded to that in the matched migraine patients. Nucleus cuneiformis (NCF), a component of brainstem pain modulatory circuits, appears to be hypofunctional in migraineurs. 3 out of the 4 thermal stimulus conditions showed significantly greater NCF activation in control subjects than the migraine patients. CONCLUSIONS: Altered descending modulation has been postulated to contribute to migraine, leading to loss of inhibition or enhanced facilitation resulting in hyperexcitability of trigeminovascular neurons. NCF function could potentially serve as a diagnostic measure in migraine patients, even when not experiencing an attack. This has important implications for the evaluation of therapies for migraine. Public Library of Science 2008-11-24 /pmc/articles/PMC2582961/ /pubmed/19030105 http://dx.doi.org/10.1371/journal.pone.0003799 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Moulton, Eric A.
Burstein, Rami
Tully, Shannon
Hargreaves, Richard
Becerra, Lino
Borsook, David
Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients
title Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients
title_full Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients
title_fullStr Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients
title_full_unstemmed Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients
title_short Interictal Dysfunction of a Brainstem Descending Modulatory Center in Migraine Patients
title_sort interictal dysfunction of a brainstem descending modulatory center in migraine patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582961/
https://www.ncbi.nlm.nih.gov/pubmed/19030105
http://dx.doi.org/10.1371/journal.pone.0003799
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