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Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system
BACKGROUND: Clinical observations suggest that hyperinsulinemia and insulin resistance can be associated with migraine headache. In the present study we examined the effect of insulin on transient receptor potential vanilloid 1 (TRPV1) receptor-dependent meningeal nociceptor functions in rats. METHO...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903670/ https://www.ncbi.nlm.nih.gov/pubmed/35033025 http://dx.doi.org/10.1186/s10194-021-01380-x |
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author | Rosta, Judit Tóth, Máté Friedrich, Nadine Sántha, Péter Jancsó, Gábor Dux, Mária |
author_facet | Rosta, Judit Tóth, Máté Friedrich, Nadine Sántha, Péter Jancsó, Gábor Dux, Mária |
author_sort | Rosta, Judit |
collection | PubMed |
description | BACKGROUND: Clinical observations suggest that hyperinsulinemia and insulin resistance can be associated with migraine headache. In the present study we examined the effect of insulin on transient receptor potential vanilloid 1 (TRPV1) receptor-dependent meningeal nociceptor functions in rats. METHODS: The effects of insulin on the TRPV1 receptor stimulation-induced release of calcitonin gene related peptide (CGRP) from trigeminal afferents and changes in meningeal blood flow were studied. Colocalization of the insulin receptor, the TRPV1 receptor and CGRP was also analyzed in trigeminal ganglion neurons. RESULTS: Insulin induced release of CGRP from meningeal afferents and consequent increases in dural blood flow through the activation of TRPV1 receptors of trigeminal afferents. Insulin sensitized both neural and vascular TRPV1 receptors making them more susceptible to the receptor agonist capsaicin. Immunohistochemistry revealed colocalization of the insulin receptor with the TRPV1 receptor and CGRP in a significant proportion of trigeminal ganglion neurons. CONCLUSIONS: Insulin may activate or sensitize meningeal nociceptors that may lead to enhanced headache susceptibility in persons with increased plasma insulin concentration. |
format | Online Article Text |
id | pubmed-8903670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Milan |
record_format | MEDLINE/PubMed |
spelling | pubmed-89036702022-03-18 Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system Rosta, Judit Tóth, Máté Friedrich, Nadine Sántha, Péter Jancsó, Gábor Dux, Mária J Headache Pain Research Article BACKGROUND: Clinical observations suggest that hyperinsulinemia and insulin resistance can be associated with migraine headache. In the present study we examined the effect of insulin on transient receptor potential vanilloid 1 (TRPV1) receptor-dependent meningeal nociceptor functions in rats. METHODS: The effects of insulin on the TRPV1 receptor stimulation-induced release of calcitonin gene related peptide (CGRP) from trigeminal afferents and changes in meningeal blood flow were studied. Colocalization of the insulin receptor, the TRPV1 receptor and CGRP was also analyzed in trigeminal ganglion neurons. RESULTS: Insulin induced release of CGRP from meningeal afferents and consequent increases in dural blood flow through the activation of TRPV1 receptors of trigeminal afferents. Insulin sensitized both neural and vascular TRPV1 receptors making them more susceptible to the receptor agonist capsaicin. Immunohistochemistry revealed colocalization of the insulin receptor with the TRPV1 receptor and CGRP in a significant proportion of trigeminal ganglion neurons. CONCLUSIONS: Insulin may activate or sensitize meningeal nociceptors that may lead to enhanced headache susceptibility in persons with increased plasma insulin concentration. Springer Milan 2022-01-15 /pmc/articles/PMC8903670/ /pubmed/35033025 http://dx.doi.org/10.1186/s10194-021-01380-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Rosta, Judit Tóth, Máté Friedrich, Nadine Sántha, Péter Jancsó, Gábor Dux, Mária Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system |
title | Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system |
title_full | Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system |
title_fullStr | Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system |
title_full_unstemmed | Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system |
title_short | Insulin sensitizes neural and vascular TRPV1 receptors in the trigeminovascular system |
title_sort | insulin sensitizes neural and vascular trpv1 receptors in the trigeminovascular system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903670/ https://www.ncbi.nlm.nih.gov/pubmed/35033025 http://dx.doi.org/10.1186/s10194-021-01380-x |
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