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A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice
BACKGROUND: Stress-induced mental illnesses (mediated by neuroinflammation) pose one of the world’s most urgent public health challenges. A reliable in vivo chemical biomarker of stress would significantly improve the clinical communities’ diagnostic and therapeutic approaches to illnesses, such as...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235270/ https://www.ncbi.nlm.nih.gov/pubmed/35761344 http://dx.doi.org/10.1186/s12974-022-02508-9 |
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author | Hersey, Melinda Reneaux, Melissa Berger, Shane N. Mena, Sergio Buchanan, Anna Marie Ou, Yangguang Tavakoli, Navid Reagan, Lawrence P. Clopath, Claudia Hashemi, Parastoo |
author_facet | Hersey, Melinda Reneaux, Melissa Berger, Shane N. Mena, Sergio Buchanan, Anna Marie Ou, Yangguang Tavakoli, Navid Reagan, Lawrence P. Clopath, Claudia Hashemi, Parastoo |
author_sort | Hersey, Melinda |
collection | PubMed |
description | BACKGROUND: Stress-induced mental illnesses (mediated by neuroinflammation) pose one of the world’s most urgent public health challenges. A reliable in vivo chemical biomarker of stress would significantly improve the clinical communities’ diagnostic and therapeutic approaches to illnesses, such as depression. METHODS: Male and female C57BL/6J mice underwent a chronic stress paradigm. We paired innovative in vivo serotonin and histamine voltammetric measurement technologies, behavioral testing, and cutting-edge mathematical methods to correlate chemistry to stress and behavior. RESULTS: Inflammation-induced increases in hypothalamic histamine were co-measured with decreased in vivo extracellular hippocampal serotonin in mice that underwent a chronic stress paradigm, regardless of behavioral phenotype. In animals with depression phenotypes, correlations were found between serotonin and the extent of behavioral indices of depression. We created a high accuracy algorithm that could predict whether animals had been exposed to stress or not based solely on the serotonin measurement. We next developed a model of serotonin and histamine modulation, which predicted that stress-induced neuroinflammation increases histaminergic activity, serving to inhibit serotonin. Finally, we created a mathematical index of stress, S(i) and predicted that during chronic stress, where S(i) is high, simultaneously increasing serotonin and decreasing histamine is the most effective chemical strategy to restoring serotonin to pre-stress levels. When we pursued this idea pharmacologically, our experiments were nearly identical to the model’s predictions. CONCLUSIONS: This work shines the light on two biomarkers of chronic stress, histamine and serotonin, and implies that both may be important in our future investigations of the pathology and treatment of inflammation-induced depression. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-022-02508-9. |
format | Online Article Text |
id | pubmed-9235270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92352702022-06-28 A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice Hersey, Melinda Reneaux, Melissa Berger, Shane N. Mena, Sergio Buchanan, Anna Marie Ou, Yangguang Tavakoli, Navid Reagan, Lawrence P. Clopath, Claudia Hashemi, Parastoo J Neuroinflammation Research BACKGROUND: Stress-induced mental illnesses (mediated by neuroinflammation) pose one of the world’s most urgent public health challenges. A reliable in vivo chemical biomarker of stress would significantly improve the clinical communities’ diagnostic and therapeutic approaches to illnesses, such as depression. METHODS: Male and female C57BL/6J mice underwent a chronic stress paradigm. We paired innovative in vivo serotonin and histamine voltammetric measurement technologies, behavioral testing, and cutting-edge mathematical methods to correlate chemistry to stress and behavior. RESULTS: Inflammation-induced increases in hypothalamic histamine were co-measured with decreased in vivo extracellular hippocampal serotonin in mice that underwent a chronic stress paradigm, regardless of behavioral phenotype. In animals with depression phenotypes, correlations were found between serotonin and the extent of behavioral indices of depression. We created a high accuracy algorithm that could predict whether animals had been exposed to stress or not based solely on the serotonin measurement. We next developed a model of serotonin and histamine modulation, which predicted that stress-induced neuroinflammation increases histaminergic activity, serving to inhibit serotonin. Finally, we created a mathematical index of stress, S(i) and predicted that during chronic stress, where S(i) is high, simultaneously increasing serotonin and decreasing histamine is the most effective chemical strategy to restoring serotonin to pre-stress levels. When we pursued this idea pharmacologically, our experiments were nearly identical to the model’s predictions. CONCLUSIONS: This work shines the light on two biomarkers of chronic stress, histamine and serotonin, and implies that both may be important in our future investigations of the pathology and treatment of inflammation-induced depression. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-022-02508-9. BioMed Central 2022-06-27 /pmc/articles/PMC9235270/ /pubmed/35761344 http://dx.doi.org/10.1186/s12974-022-02508-9 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 Hersey, Melinda Reneaux, Melissa Berger, Shane N. Mena, Sergio Buchanan, Anna Marie Ou, Yangguang Tavakoli, Navid Reagan, Lawrence P. Clopath, Claudia Hashemi, Parastoo A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
title | A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
title_full | A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
title_fullStr | A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
title_full_unstemmed | A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
title_short | A tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
title_sort | tale of two transmitters: serotonin and histamine as in vivo biomarkers of chronic stress in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235270/ https://www.ncbi.nlm.nih.gov/pubmed/35761344 http://dx.doi.org/10.1186/s12974-022-02508-9 |
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