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Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation
BACKGROUND: Determining the etiology and possible treatment strategies for numerous diseases requires a comprehensive understanding of compensatory mechanisms in physiological systems. The vagus nerve acts as a key interface between the brain and the peripheral internal organs. We set out to identif...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642550/ https://www.ncbi.nlm.nih.gov/pubmed/31324250 http://dx.doi.org/10.1186/s12974-019-1544-y |
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author | Kobrzycka, Anna Napora, Paweł Pearson, Brandon L. Pierzchała-Koziec, Krystyna Szewczyk, Rafał Wieczorek, Marek |
author_facet | Kobrzycka, Anna Napora, Paweł Pearson, Brandon L. Pierzchała-Koziec, Krystyna Szewczyk, Rafał Wieczorek, Marek |
author_sort | Kobrzycka, Anna |
collection | PubMed |
description | BACKGROUND: Determining the etiology and possible treatment strategies for numerous diseases requires a comprehensive understanding of compensatory mechanisms in physiological systems. The vagus nerve acts as a key interface between the brain and the peripheral internal organs. We set out to identify mechanisms compensating for a lack of neuronal communication between the immune and the central nervous system (CNS) during infection. METHODS: We assessed biochemical and central neurotransmitter changes resulting from subdiaphragmatic vagotomy and whether they are modulated by intraperitoneal infection. We performed a series of subdiaphragmatic vagotomy or sham operations on male Wistar rats. Next, after full, 30-day recovery period, they were randomly assigned to receive an injection of Escherichia coli lipopolysaccharide or saline. Two hours later, animal were euthanized and we measured the plasma concentration of prostaglandin E2 (with HPLC-MS), interleukin-6 (ELISA), and corticosterone (RIA). We also had measured the concentration of monoaminergic neurotransmitters and their metabolites in the amygdala, brainstem, hippocampus, hypothalamus, motor cortex, periaqueductal gray, and prefrontal medial cortex using RP-HPLC-ED. A subset of the animals was evaluated in the elevated plus maze test immediately before euthanization. RESULTS: The lack of immunosensory signaling of the vagus nerve stimulated increased activity of discrete inflammatory marker signals, which we confirmed by quantifying biochemical changes in blood plasma. Behavioral results, although preliminary, support the observed biochemical alterations. Many of the neurotransmitter changes observed after vagotomy indicated that the vagus nerve influences the activity of many brain areas involved in control of immune response and sickness behavior. Our studies show that these changes are largely eliminated during experimental infection. CONCLUSIONS: Our results suggest that in vagotomized animals with blocked CNS, communication may transmit via a pathway independent of the vagus nerve to permit restoration of CNS activity for peripheral inflammation control. |
format | Online Article Text |
id | pubmed-6642550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66425502019-07-29 Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation Kobrzycka, Anna Napora, Paweł Pearson, Brandon L. Pierzchała-Koziec, Krystyna Szewczyk, Rafał Wieczorek, Marek J Neuroinflammation Research BACKGROUND: Determining the etiology and possible treatment strategies for numerous diseases requires a comprehensive understanding of compensatory mechanisms in physiological systems. The vagus nerve acts as a key interface between the brain and the peripheral internal organs. We set out to identify mechanisms compensating for a lack of neuronal communication between the immune and the central nervous system (CNS) during infection. METHODS: We assessed biochemical and central neurotransmitter changes resulting from subdiaphragmatic vagotomy and whether they are modulated by intraperitoneal infection. We performed a series of subdiaphragmatic vagotomy or sham operations on male Wistar rats. Next, after full, 30-day recovery period, they were randomly assigned to receive an injection of Escherichia coli lipopolysaccharide or saline. Two hours later, animal were euthanized and we measured the plasma concentration of prostaglandin E2 (with HPLC-MS), interleukin-6 (ELISA), and corticosterone (RIA). We also had measured the concentration of monoaminergic neurotransmitters and their metabolites in the amygdala, brainstem, hippocampus, hypothalamus, motor cortex, periaqueductal gray, and prefrontal medial cortex using RP-HPLC-ED. A subset of the animals was evaluated in the elevated plus maze test immediately before euthanization. RESULTS: The lack of immunosensory signaling of the vagus nerve stimulated increased activity of discrete inflammatory marker signals, which we confirmed by quantifying biochemical changes in blood plasma. Behavioral results, although preliminary, support the observed biochemical alterations. Many of the neurotransmitter changes observed after vagotomy indicated that the vagus nerve influences the activity of many brain areas involved in control of immune response and sickness behavior. Our studies show that these changes are largely eliminated during experimental infection. CONCLUSIONS: Our results suggest that in vagotomized animals with blocked CNS, communication may transmit via a pathway independent of the vagus nerve to permit restoration of CNS activity for peripheral inflammation control. BioMed Central 2019-07-19 /pmc/articles/PMC6642550/ /pubmed/31324250 http://dx.doi.org/10.1186/s12974-019-1544-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Kobrzycka, Anna Napora, Paweł Pearson, Brandon L. Pierzchała-Koziec, Krystyna Szewczyk, Rafał Wieczorek, Marek Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
title | Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
title_full | Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
title_fullStr | Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
title_full_unstemmed | Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
title_short | Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
title_sort | peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642550/ https://www.ncbi.nlm.nih.gov/pubmed/31324250 http://dx.doi.org/10.1186/s12974-019-1544-y |
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