Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kobrzycka, Anna, Napora, Paweł, Pearson, Brandon L., Pierzchała-Koziec, Krystyna, Szewczyk, Rafał, Wieczorek, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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
_version_ 1783436998325829632
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
work_keys_str_mv AT kobrzyckaanna peripheralandcentralcompensatorymechanismsforimpairedvagusnervefunctionduringperipheralimmuneactivation
AT naporapaweł peripheralandcentralcompensatorymechanismsforimpairedvagusnervefunctionduringperipheralimmuneactivation
AT pearsonbrandonl peripheralandcentralcompensatorymechanismsforimpairedvagusnervefunctionduringperipheralimmuneactivation
AT pierzchałakozieckrystyna peripheralandcentralcompensatorymechanismsforimpairedvagusnervefunctionduringperipheralimmuneactivation
AT szewczykrafał peripheralandcentralcompensatorymechanismsforimpairedvagusnervefunctionduringperipheralimmuneactivation
AT wieczorekmarek peripheralandcentralcompensatorymechanismsforimpairedvagusnervefunctionduringperipheralimmuneactivation