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An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger
Histamine is well known for mediating peripheral inflammation; however, this amine is also found in high concentrations in the brain where its roles are much less known. In vivo chemical dynamics are difficult to measure, thus fundamental aspects of histamine’s neurochemistry remain undefined. In th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738190/ https://www.ncbi.nlm.nih.gov/pubmed/36499189 http://dx.doi.org/10.3390/ijms232314862 |
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author | Berger, Shane N. Baumberger, Beatrice Samaranayake, Srimal Hersey, Melinda Mena, Sergio Bain, Ian Duncan, William Reed, Michael C. Nijhout, H. Frederik Best, Janet Hashemi, Parastoo |
author_facet | Berger, Shane N. Baumberger, Beatrice Samaranayake, Srimal Hersey, Melinda Mena, Sergio Bain, Ian Duncan, William Reed, Michael C. Nijhout, H. Frederik Best, Janet Hashemi, Parastoo |
author_sort | Berger, Shane N. |
collection | PubMed |
description | Histamine is well known for mediating peripheral inflammation; however, this amine is also found in high concentrations in the brain where its roles are much less known. In vivo chemical dynamics are difficult to measure, thus fundamental aspects of histamine’s neurochemistry remain undefined. In this work, we undertake the first in-depth characterization of real time in vivo histamine dynamics using fast electrochemical tools. We find that histamine release is sensitive to pharmacological manipulation at the level of synthesis, packaging, autoreceptors and metabolism. We find two breakthrough aspects of histamine modulation. First, differences in H3 receptor regulation between sexes show that histamine release in female mice is much more tightly regulated than in male mice under H3 or inflammatory drug challenge. We hypothesize that this finding may contribute to hormone-mediated neuroprotection mechanisms in female mice. Second, a high dose of a commonly available antihistamine, the H1 receptor inverse agonist diphenhydramine, rapidly decreases serotonin levels. This finding highlights the sheer significance of pharmaceuticals on neuromodulation. Our study opens the path to better understanding and treating histamine related disorders of the brain (such as neuroinflammation), emphasizing that sex and modulation (of serotonin) are critical factors to consider when studying/designing new histamine targeting therapeutics. |
format | Online Article Text |
id | pubmed-9738190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97381902022-12-11 An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger Berger, Shane N. Baumberger, Beatrice Samaranayake, Srimal Hersey, Melinda Mena, Sergio Bain, Ian Duncan, William Reed, Michael C. Nijhout, H. Frederik Best, Janet Hashemi, Parastoo Int J Mol Sci Article Histamine is well known for mediating peripheral inflammation; however, this amine is also found in high concentrations in the brain where its roles are much less known. In vivo chemical dynamics are difficult to measure, thus fundamental aspects of histamine’s neurochemistry remain undefined. In this work, we undertake the first in-depth characterization of real time in vivo histamine dynamics using fast electrochemical tools. We find that histamine release is sensitive to pharmacological manipulation at the level of synthesis, packaging, autoreceptors and metabolism. We find two breakthrough aspects of histamine modulation. First, differences in H3 receptor regulation between sexes show that histamine release in female mice is much more tightly regulated than in male mice under H3 or inflammatory drug challenge. We hypothesize that this finding may contribute to hormone-mediated neuroprotection mechanisms in female mice. Second, a high dose of a commonly available antihistamine, the H1 receptor inverse agonist diphenhydramine, rapidly decreases serotonin levels. This finding highlights the sheer significance of pharmaceuticals on neuromodulation. Our study opens the path to better understanding and treating histamine related disorders of the brain (such as neuroinflammation), emphasizing that sex and modulation (of serotonin) are critical factors to consider when studying/designing new histamine targeting therapeutics. MDPI 2022-11-28 /pmc/articles/PMC9738190/ /pubmed/36499189 http://dx.doi.org/10.3390/ijms232314862 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Berger, Shane N. Baumberger, Beatrice Samaranayake, Srimal Hersey, Melinda Mena, Sergio Bain, Ian Duncan, William Reed, Michael C. Nijhout, H. Frederik Best, Janet Hashemi, Parastoo An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger |
title | An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger |
title_full | An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger |
title_fullStr | An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger |
title_full_unstemmed | An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger |
title_short | An In Vivo Definition of Brain Histamine Dynamics Reveals Critical Neuromodulatory Roles for This Elusive Messenger |
title_sort | in vivo definition of brain histamine dynamics reveals critical neuromodulatory roles for this elusive messenger |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738190/ https://www.ncbi.nlm.nih.gov/pubmed/36499189 http://dx.doi.org/10.3390/ijms232314862 |
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