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Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling

Abdominal pain is common in patients with active inflammation of the colon but can persist even in its absence, suggesting other mechanisms of pain signaling. Recent findings suggest colon epithelial cells are direct regulators of pain-sensing neurons. Optogenetic activation of epithelial cells evok...

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Detalles Bibliográficos
Autores principales: Najjar, Sarah A, Albers, Kathryn M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600958/
https://www.ncbi.nlm.nih.gov/pubmed/34805983
http://dx.doi.org/10.1093/crocol/otab040
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author Najjar, Sarah A
Albers, Kathryn M
author_facet Najjar, Sarah A
Albers, Kathryn M
author_sort Najjar, Sarah A
collection PubMed
description Abdominal pain is common in patients with active inflammation of the colon but can persist even in its absence, suggesting other mechanisms of pain signaling. Recent findings suggest colon epithelial cells are direct regulators of pain-sensing neurons. Optogenetic activation of epithelial cells evoked nerve firing and pain-like behaviors. Inhibition of epithelial cells caused the opposite effect, reducing responses to colon distension and inflammatory hypersensitivity. Thus, epithelial cells alone can regulate the activation of pain circuits. Future goals are to define the anatomical and cellular mechanisms that underlie epithelial–neural pain signaling and how it is altered in response to colon inflammation.
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spelling pubmed-86009582021-11-18 Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling Najjar, Sarah A Albers, Kathryn M Crohns Colitis 360 Review Articles Abdominal pain is common in patients with active inflammation of the colon but can persist even in its absence, suggesting other mechanisms of pain signaling. Recent findings suggest colon epithelial cells are direct regulators of pain-sensing neurons. Optogenetic activation of epithelial cells evoked nerve firing and pain-like behaviors. Inhibition of epithelial cells caused the opposite effect, reducing responses to colon distension and inflammatory hypersensitivity. Thus, epithelial cells alone can regulate the activation of pain circuits. Future goals are to define the anatomical and cellular mechanisms that underlie epithelial–neural pain signaling and how it is altered in response to colon inflammation. Oxford University Press 2021-07-07 /pmc/articles/PMC8600958/ /pubmed/34805983 http://dx.doi.org/10.1093/crocol/otab040 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Crohn's & Colitis Foundation. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Review Articles
Najjar, Sarah A
Albers, Kathryn M
Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling
title Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling
title_full Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling
title_fullStr Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling
title_full_unstemmed Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling
title_short Pain in Inflammatory Bowel Disease: Optogenetic Strategies for Study of Neural–Epithelial Signaling
title_sort pain in inflammatory bowel disease: optogenetic strategies for study of neural–epithelial signaling
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600958/
https://www.ncbi.nlm.nih.gov/pubmed/34805983
http://dx.doi.org/10.1093/crocol/otab040
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