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Muscle Injury Induces Postoperative Cognitive Dysfunction

Postoperative cognitive dysfunction (POCD) is a major complication affecting patients of any age undergoing surgery. This syndrome impacts everyday life up to months after hospital discharge, and its pathophysiology still remains unclear. Translational research focusing on POCD is based on a wide va...

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Autores principales: Guéniot, Lorna, Lepere, Victoria, De Medeiros, Gabriela Ferreira, Danckaert, Anne, Flamant, Patricia, Le Dudal, Marine, Langeron, Olivier, Goossens, Pierre L., Chrétien, Fabrice, Jouvion, Grégory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026159/
https://www.ncbi.nlm.nih.gov/pubmed/32066806
http://dx.doi.org/10.1038/s41598-020-59639-3
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author Guéniot, Lorna
Lepere, Victoria
De Medeiros, Gabriela Ferreira
Danckaert, Anne
Flamant, Patricia
Le Dudal, Marine
Langeron, Olivier
Goossens, Pierre L.
Chrétien, Fabrice
Jouvion, Grégory
author_facet Guéniot, Lorna
Lepere, Victoria
De Medeiros, Gabriela Ferreira
Danckaert, Anne
Flamant, Patricia
Le Dudal, Marine
Langeron, Olivier
Goossens, Pierre L.
Chrétien, Fabrice
Jouvion, Grégory
author_sort Guéniot, Lorna
collection PubMed
description Postoperative cognitive dysfunction (POCD) is a major complication affecting patients of any age undergoing surgery. This syndrome impacts everyday life up to months after hospital discharge, and its pathophysiology still remains unclear. Translational research focusing on POCD is based on a wide variety of rodent models, such as the murine tibial fracture, whose severity can limit mouse locomotion and proper behavioral assessment. Besides, influence of skeletal muscle injury, a lesion encountered in a wide range of surgeries, has not been explored in POCD occurrence. We propose a physical model of muscle injury in CX3CR1(GFP/+) mice (displaying green fluorescent microglial cells) to study POCD, with morphological, behavioral and molecular approaches. We highlighted: alteration of short- and long-term memory after muscle regeneration, wide microglial reactivity in the brain, including hippocampus area, 24 hours after muscle injury, and an alteration of central brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF) balance, 28 days after muscle injury. Our results suggest for the first time that muscle injury can have early as well as late impacts on the brain. Our CX3CR1(GFP/+) model can also facilitate microglial investigation, more specifically their pivotal role in neuroinflammation and synaptic plasticity, in the pathophysiology of POCD.
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spelling pubmed-70261592020-02-26 Muscle Injury Induces Postoperative Cognitive Dysfunction Guéniot, Lorna Lepere, Victoria De Medeiros, Gabriela Ferreira Danckaert, Anne Flamant, Patricia Le Dudal, Marine Langeron, Olivier Goossens, Pierre L. Chrétien, Fabrice Jouvion, Grégory Sci Rep Article Postoperative cognitive dysfunction (POCD) is a major complication affecting patients of any age undergoing surgery. This syndrome impacts everyday life up to months after hospital discharge, and its pathophysiology still remains unclear. Translational research focusing on POCD is based on a wide variety of rodent models, such as the murine tibial fracture, whose severity can limit mouse locomotion and proper behavioral assessment. Besides, influence of skeletal muscle injury, a lesion encountered in a wide range of surgeries, has not been explored in POCD occurrence. We propose a physical model of muscle injury in CX3CR1(GFP/+) mice (displaying green fluorescent microglial cells) to study POCD, with morphological, behavioral and molecular approaches. We highlighted: alteration of short- and long-term memory after muscle regeneration, wide microglial reactivity in the brain, including hippocampus area, 24 hours after muscle injury, and an alteration of central brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF) balance, 28 days after muscle injury. Our results suggest for the first time that muscle injury can have early as well as late impacts on the brain. Our CX3CR1(GFP/+) model can also facilitate microglial investigation, more specifically their pivotal role in neuroinflammation and synaptic plasticity, in the pathophysiology of POCD. Nature Publishing Group UK 2020-02-17 /pmc/articles/PMC7026159/ /pubmed/32066806 http://dx.doi.org/10.1038/s41598-020-59639-3 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
Guéniot, Lorna
Lepere, Victoria
De Medeiros, Gabriela Ferreira
Danckaert, Anne
Flamant, Patricia
Le Dudal, Marine
Langeron, Olivier
Goossens, Pierre L.
Chrétien, Fabrice
Jouvion, Grégory
Muscle Injury Induces Postoperative Cognitive Dysfunction
title Muscle Injury Induces Postoperative Cognitive Dysfunction
title_full Muscle Injury Induces Postoperative Cognitive Dysfunction
title_fullStr Muscle Injury Induces Postoperative Cognitive Dysfunction
title_full_unstemmed Muscle Injury Induces Postoperative Cognitive Dysfunction
title_short Muscle Injury Induces Postoperative Cognitive Dysfunction
title_sort muscle injury induces postoperative cognitive dysfunction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026159/
https://www.ncbi.nlm.nih.gov/pubmed/32066806
http://dx.doi.org/10.1038/s41598-020-59639-3
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