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Automated and rapid self-report of nociception in transgenic mice
There are currently no rapid, operant pain behaviors in rodents that use a self-report to directly engage higher-order brain circuitry. We have developed a pain detection assay consisting of a lick behavior in response to optogenetic activation of predominantly nociceptive peripheral afferent nerve...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413385/ https://www.ncbi.nlm.nih.gov/pubmed/32764714 http://dx.doi.org/10.1038/s41598-020-70028-8 |
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author | Black, Christopher J. Allawala, Anusha B. Bloye, Kiernan Vanent, Kevin N. Edhi, Muhammad M. Saab, Carl Y. Borton, David A. |
author_facet | Black, Christopher J. Allawala, Anusha B. Bloye, Kiernan Vanent, Kevin N. Edhi, Muhammad M. Saab, Carl Y. Borton, David A. |
author_sort | Black, Christopher J. |
collection | PubMed |
description | There are currently no rapid, operant pain behaviors in rodents that use a self-report to directly engage higher-order brain circuitry. We have developed a pain detection assay consisting of a lick behavior in response to optogenetic activation of predominantly nociceptive peripheral afferent nerve fibers in head-restrained transgenic mice expressing ChR2 in TRPV1 containing neurons. TRPV1-ChR2-EYFP mice (n = 5) were trained to provide lick reports to the detection of light-evoked nociceptive stimulation to the hind paw. Using simultaneous video recording, we demonstrate that the learned lick behavior may prove more pertinent in investigating brain driven pain processes than the reflex behavior. Within sessions, the response bias of transgenic mice changed with respect to lick behavior but not reflex behavior. Furthermore, response similarity between the lick and reflex behaviors diverged near perceptual threshold. Our nociceptive lick-report detection assay will enable a host of investigations into the millisecond, single cell, neural dynamics underlying pain processing in the central nervous system of awake behaving animals. |
format | Online Article Text |
id | pubmed-7413385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74133852020-08-10 Automated and rapid self-report of nociception in transgenic mice Black, Christopher J. Allawala, Anusha B. Bloye, Kiernan Vanent, Kevin N. Edhi, Muhammad M. Saab, Carl Y. Borton, David A. Sci Rep Article There are currently no rapid, operant pain behaviors in rodents that use a self-report to directly engage higher-order brain circuitry. We have developed a pain detection assay consisting of a lick behavior in response to optogenetic activation of predominantly nociceptive peripheral afferent nerve fibers in head-restrained transgenic mice expressing ChR2 in TRPV1 containing neurons. TRPV1-ChR2-EYFP mice (n = 5) were trained to provide lick reports to the detection of light-evoked nociceptive stimulation to the hind paw. Using simultaneous video recording, we demonstrate that the learned lick behavior may prove more pertinent in investigating brain driven pain processes than the reflex behavior. Within sessions, the response bias of transgenic mice changed with respect to lick behavior but not reflex behavior. Furthermore, response similarity between the lick and reflex behaviors diverged near perceptual threshold. Our nociceptive lick-report detection assay will enable a host of investigations into the millisecond, single cell, neural dynamics underlying pain processing in the central nervous system of awake behaving animals. Nature Publishing Group UK 2020-08-06 /pmc/articles/PMC7413385/ /pubmed/32764714 http://dx.doi.org/10.1038/s41598-020-70028-8 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Black, Christopher J. Allawala, Anusha B. Bloye, Kiernan Vanent, Kevin N. Edhi, Muhammad M. Saab, Carl Y. Borton, David A. Automated and rapid self-report of nociception in transgenic mice |
title | Automated and rapid self-report of nociception in transgenic mice |
title_full | Automated and rapid self-report of nociception in transgenic mice |
title_fullStr | Automated and rapid self-report of nociception in transgenic mice |
title_full_unstemmed | Automated and rapid self-report of nociception in transgenic mice |
title_short | Automated and rapid self-report of nociception in transgenic mice |
title_sort | automated and rapid self-report of nociception in transgenic mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413385/ https://www.ncbi.nlm.nih.gov/pubmed/32764714 http://dx.doi.org/10.1038/s41598-020-70028-8 |
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