Evidence map›Paper›PMID 25128387›Full record

ArticleBrain, behavior, and immunity2015

Vagal nerve stimulation blocks interleukin 6-dependent synaptic hyperexcitability induced by lipopolysaccharide-induced acute stress in the rodent prefrontal cortex.

Francisco Garcia-Oscos, David Peña, Mohammad Housini, Derek Cheng, Diego Lopez, Michael S Borland, Roberto Salgado-Delgado, Humberto Salgado, Santosh D'Mello, Michael P Kilgard and 2 more

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  7. Microglia in depression: current perspectives.Science China. Life sciences · 2021
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  10. Inflammation, Self-Regulation, and Health: An Immunologic Model of Self-Regulatory Failure.Perspectives on psychological science : a journal of the Association for Psychological Science · 2017
    Review
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  13. The role of the gut-brain axis in alcohol use disorders.Progress in neuro-psychopharmacology & biological psychiatry · 2016
    Review
  14. Article
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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

12 authors at 6 institutions in 3 countries.

Francisco Garcia-OscosUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States; University of Texas Southwestern, Department of Psychiatry, Dallas, TX, United States. Electronic address: franciscooscos86@hotmail.com.
David PeñaUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States.
Mohammad HousiniUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States.
Derek ChengUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States.
Diego LopezUniversity of Texas at Arlington, Department of Chemistry and Biochemistry, Arlington, TX, United States.
Michael S BorlandUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States.
Roberto Salgado-DelgadoUniversidad Autónoma de San Luis Potosí, Facultad de Ciencias, San Luis Potosí, Mexico.
Humberto SalgadoUniversidad Autónoma de Yucatán, Centro de Investigaciones Regionales Hideyo Noguchi, Mérida, Yucatán, Mexico.
Santosh D'MelloUniversity of Texas at Dallas, School of Natural Sciences and Mathematics, Richardson, TX, United States; Southern Methodist University, Department of Neuroscience, Dallas, TX, United States.
Michael P KilgardUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States.
Stefan Rose-JohnChristian Albrecht University, Department of Biochemistry, Kiel, Germany.
Marco AtzoriUniversity of Texas at Dallas, School of Behavioral and Brain Sciences, Richardson, TX, United States; Universidad Autónoma de San Luis Potosí, Facultad de Ciencias, San Luis Potosí, Mexico. Electronic address: marco.atzori@uaslp.mx.
The University of Texas at Dallas · USAutonomous University of San Luis Potosí · MXAutonomous University of Yucatán · MXKiel University · DEThe University of Texas at Arlington · USThe University of Texas Southwestern Medical Center · US

Funding

Signaling Pathways Regulating Neuronal SurvivalR01NS040408 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI D'MELLO, SANTOSH R · 2002 to 2018
$4.8M
NINDS NIH HHS R01 NS040408
6 · The paper itself

Abstract

The ratio between synaptic inhibition and excitation (sI/E) is a critical factor in the pathophysiology of neuropsychiatric disease. We recently described a stress-induced interleukin-6 dependent mechanism leading to a decrease in sI/E in the rodent temporal cortex. The aim of the present study was to determine whether a similar mechanism takes place in the prefrontal cortex, and to elaborate strategies to prevent or attenuate it. We used aseptic inflammation (single acute injections of lipopolysaccharide, LPS, 10mg/kg) as stress model, and patch-clamp recording on a prefrontal cortical slice preparation from wild-type rat and mice, as well as from transgenic mice in which the inhibitor of IL-6 trans-signaling sgp130Fc was produced in a brain-specific fashion (sgp130Fc mice). The anti-inflammatory reflex was activated either by vagal nerve stimulation or peripheral administration of the nicotinic α7 receptor agonist PHA543613. We found that the IL-6-dependent reduction in prefrontal cortex synaptic inhibition was blocked in sgp130Fc mice, or - in wild-type animals - upon application sgp130Fc. Similar results were obtained by activating the "anti-inflammatory reflex" - a neural circuit regulating peripheral immune response - by stimulation of the vagal nerve or through peripheral administration of the α7 nicotinic receptor agonist PHA543613. Our results indicate that the prefrontal cortex is an important potential target of IL-6 mediated trans-signaling, and suggest a potential new avenue in the treatment of a large class of hyperexcitable neuropsychiatric conditions, including epilepsy, schizophrenic psychoses, anxiety disorders, autism spectrum disorders, and depression.

Indexed as

Vagus Nerve StimulationAnimalsDisease Models, AnimalInflammationInterleukin-6LipopolysaccharidesMiceNeural InhibitionPrefrontal CortexRatsRats, Sprague-DawleyStress, PhysiologicalSynapsesInterleukin-6LipopolysaccharidesAnti-inflammatory reflexGABAInterleukin 6LipopolysaccharideVagal nerve stimulation

Identifiers

PMID25128387
PMCPMC4727901
OpenAlexW2064117534

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.