Evidence map›Paper›PMID 31324250›Full record

ArticleJournal of neuroinflammation2019

Peripheral and central compensatory mechanisms for impaired vagus nerve function during peripheral immune activation.

Anna Kobrzycka, Paweł Napora, Brandon L Pearson, Krystyna Pierzchała-Koziec, Rafał Szewczyk, Marek Wieczorek

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Role of macrophages in neuroimmune regulation.Frontiers in immunology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Anna KobrzyckaDepartment of Neurobiology, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland. anna.kobrzycka@biol.uni.lodz.pl.
Paweł NaporaDepartment of Neurobiology, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Brandon L PearsonDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, USA.
Krystyna Pierzchała-KoziecDepartment of Animal Physiology and Endocrinology, University of Agriculture, Krakow, Poland.
Rafał SzewczykDepartment of Industrial Microbiology and Biotechnology, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Marek WieczorekDepartment of Neurobiology, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland. marek.wieczorek@biol.uni.lodz.pl.ORCID http://orcid.org/0000-0002-0862-8076
University of Łódź · PLColumbia University · USUniversity of Agriculture in Krakow · PL

Funding

Polish National Science Center UMO 2012/07/B/NZ4/00205
6 · The paper itself

Abstract

backgroundDetermining 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.

methodsWe 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.

resultsThe 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.

conclusionsOur 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.

Indexed as

AnimalsBrainInflammationLipopolysaccharidesMaleNeuroimmunomodulationRatsRats, WistarVagotomyVagus NerveLipopolysaccharidesCNS communicationCompensatory mechanismsElevated plus maze testLPSPGE2Prostaglandin E2Sickness behaviorVagotomyVagus nerve

Identifiers

PMID31324250
PMCPMC6642550
OpenAlexW2963105844

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.