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The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine

BACKGROUND: Recent work, both clinical and experimental, suggests that the hypothalamic hormone oxytocin (OT) and its receptor (OTR) may be involved in migraine pathophysiology. In order to better understand possible central actions of OT in migraine/headache pathogenesis, we mapped the distribution...

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Autores principales: Warfvinge, Karin, Krause, Diana, Edvinsson, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006173/
https://www.ncbi.nlm.nih.gov/pubmed/32028899
http://dx.doi.org/10.1186/s10194-020-1079-8
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author Warfvinge, Karin
Krause, Diana
Edvinsson, Lars
author_facet Warfvinge, Karin
Krause, Diana
Edvinsson, Lars
author_sort Warfvinge, Karin
collection PubMed
description BACKGROUND: Recent work, both clinical and experimental, suggests that the hypothalamic hormone oxytocin (OT) and its receptor (OTR) may be involved in migraine pathophysiology. In order to better understand possible central actions of OT in migraine/headache pathogenesis, we mapped the distribution of OT and OTR in nerve cells and fibers in rat brain with a focus on areas related to migraine attacks and/or shown previously to contain calcitonin gene related peptide (CGRP), another neuropeptide involved in migraine. METHODS: Distribution of OT and OTR in the adult, rat brain was qualitatively examined with immunohistochemistry using a series of well characterized specific antibodies. RESULTS: As expected, OT was extensively localized in the cell somas of two hypothalamic nuclei, the supraoptic (SO or SON) and paraventricular nuclei (Pa or PVN). OT also was found in many other regions of the brain where it was localized mainly in nerve fibers. In contrast, OTR staining in the brain was mainly observed in cell somas with very little expression in fibers. The most distinct OTR expression was found in the hippocampus, the pons and the substantia nigra. In some regions of the brain (e.g. the amygdala and the hypothalamus), both OT and OTR were expressed (match). Mismatch between the peptide and its receptor was primarily observed in the cerebral and cerebellar cortex (OT expression) and hippocampus (OTR expression). CONCLUSIONS: We compared OT/OTR distribution in the CNS with that of CGRP and identified regions related to migraine. In particular, regions suggested as “migraine generators”, showed correspondence among the three mappings. These findings suggest central OT pathways may contribute to the role of the hypothalamus in migraine attacks.
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spelling pubmed-70061732020-02-11 The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine Warfvinge, Karin Krause, Diana Edvinsson, Lars J Headache Pain Research Article BACKGROUND: Recent work, both clinical and experimental, suggests that the hypothalamic hormone oxytocin (OT) and its receptor (OTR) may be involved in migraine pathophysiology. In order to better understand possible central actions of OT in migraine/headache pathogenesis, we mapped the distribution of OT and OTR in nerve cells and fibers in rat brain with a focus on areas related to migraine attacks and/or shown previously to contain calcitonin gene related peptide (CGRP), another neuropeptide involved in migraine. METHODS: Distribution of OT and OTR in the adult, rat brain was qualitatively examined with immunohistochemistry using a series of well characterized specific antibodies. RESULTS: As expected, OT was extensively localized in the cell somas of two hypothalamic nuclei, the supraoptic (SO or SON) and paraventricular nuclei (Pa or PVN). OT also was found in many other regions of the brain where it was localized mainly in nerve fibers. In contrast, OTR staining in the brain was mainly observed in cell somas with very little expression in fibers. The most distinct OTR expression was found in the hippocampus, the pons and the substantia nigra. In some regions of the brain (e.g. the amygdala and the hypothalamus), both OT and OTR were expressed (match). Mismatch between the peptide and its receptor was primarily observed in the cerebral and cerebellar cortex (OT expression) and hippocampus (OTR expression). CONCLUSIONS: We compared OT/OTR distribution in the CNS with that of CGRP and identified regions related to migraine. In particular, regions suggested as “migraine generators”, showed correspondence among the three mappings. These findings suggest central OT pathways may contribute to the role of the hypothalamus in migraine attacks. Springer Milan 2020-02-07 /pmc/articles/PMC7006173/ /pubmed/32028899 http://dx.doi.org/10.1186/s10194-020-1079-8 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Warfvinge, Karin
Krause, Diana
Edvinsson, Lars
The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
title The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
title_full The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
title_fullStr The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
title_full_unstemmed The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
title_short The distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
title_sort distribution of oxytocin and the oxytocin receptor in rat brain: relation to regions active in migraine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006173/
https://www.ncbi.nlm.nih.gov/pubmed/32028899
http://dx.doi.org/10.1186/s10194-020-1079-8
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