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Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants
Immune function and sensitivity to pain are closely related, but the association between early life inflammation and sensory nervous system development is poorly understood—especially in humans. Here, in term-born infants, we measure brain activity and reflex withdrawal activity (using EEG and EMG)...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270448/ https://www.ncbi.nlm.nih.gov/pubmed/35803920 http://dx.doi.org/10.1038/s41467-022-31505-y |
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author | Cobo, Maria M. Green, Gabrielle Andritsou, Foteini Baxter, Luke Evans Fry, Ria Grabbe, Annika Gursul, Deniz Hoskin, Amy Mellado, Gabriela Schmidt van der Vaart, Marianne Adams, Eleri Bhatt, Aomesh Denk, Franziska Hartley, Caroline Slater, Rebeccah |
author_facet | Cobo, Maria M. Green, Gabrielle Andritsou, Foteini Baxter, Luke Evans Fry, Ria Grabbe, Annika Gursul, Deniz Hoskin, Amy Mellado, Gabriela Schmidt van der Vaart, Marianne Adams, Eleri Bhatt, Aomesh Denk, Franziska Hartley, Caroline Slater, Rebeccah |
author_sort | Cobo, Maria M. |
collection | PubMed |
description | Immune function and sensitivity to pain are closely related, but the association between early life inflammation and sensory nervous system development is poorly understood—especially in humans. Here, in term-born infants, we measure brain activity and reflex withdrawal activity (using EEG and EMG) and behavioural and physiological activity (using the PIPP-R score) to assess the impact of suspected early-onset neonatal infection on tactile- and noxious-evoked responses. We present evidence that neonatal inflammation (assessed by measuring C-reactive protein levels) is associated with increased spinal cord excitability and evoked brain activity following both tactile and noxious stimulation. There are early indications that this hyperalgesia could be maintained post-inflammation, supporting pre-clinical reports of early-life immune dysfunction influencing pain sensitivity in adults. |
format | Online Article Text |
id | pubmed-9270448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92704482022-07-10 Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants Cobo, Maria M. Green, Gabrielle Andritsou, Foteini Baxter, Luke Evans Fry, Ria Grabbe, Annika Gursul, Deniz Hoskin, Amy Mellado, Gabriela Schmidt van der Vaart, Marianne Adams, Eleri Bhatt, Aomesh Denk, Franziska Hartley, Caroline Slater, Rebeccah Nat Commun Article Immune function and sensitivity to pain are closely related, but the association between early life inflammation and sensory nervous system development is poorly understood—especially in humans. Here, in term-born infants, we measure brain activity and reflex withdrawal activity (using EEG and EMG) and behavioural and physiological activity (using the PIPP-R score) to assess the impact of suspected early-onset neonatal infection on tactile- and noxious-evoked responses. We present evidence that neonatal inflammation (assessed by measuring C-reactive protein levels) is associated with increased spinal cord excitability and evoked brain activity following both tactile and noxious stimulation. There are early indications that this hyperalgesia could be maintained post-inflammation, supporting pre-clinical reports of early-life immune dysfunction influencing pain sensitivity in adults. Nature Publishing Group UK 2022-07-08 /pmc/articles/PMC9270448/ /pubmed/35803920 http://dx.doi.org/10.1038/s41467-022-31505-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cobo, Maria M. Green, Gabrielle Andritsou, Foteini Baxter, Luke Evans Fry, Ria Grabbe, Annika Gursul, Deniz Hoskin, Amy Mellado, Gabriela Schmidt van der Vaart, Marianne Adams, Eleri Bhatt, Aomesh Denk, Franziska Hartley, Caroline Slater, Rebeccah Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
title | Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
title_full | Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
title_fullStr | Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
title_full_unstemmed | Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
title_short | Early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
title_sort | early life inflammation is associated with spinal cord excitability and nociceptive sensitivity in human infants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270448/ https://www.ncbi.nlm.nih.gov/pubmed/35803920 http://dx.doi.org/10.1038/s41467-022-31505-y |
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