Evidence map›Paper›PMID 22196984›Full record

ArticleBiological psychiatry2012

The stress-induced cytokine interleukin-6 decreases the inhibition/excitation ratio in the rat temporal cortex via trans-signaling.

Francisco Garcia-Oscos, Humberto Salgado, Shawn Hall, Feba Thomas, George E Farmer, Jorge Bermeo, Luis Charles Galindo, Ruben D Ramirez, Santosh D'Mello, Stefan Rose-John and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Biological psychiatry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

51 citing papers in PubMed, 97 citations in OpenAlex.

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  18. Microglial Cytokines Mediate Plasticity Induced by 10 Hz Repetitive Magnetic Stimulation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    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

11 authors at 4 institutions in 3 countries.

Francisco Garcia-OscosSchool of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, 75080, USA.
Humberto Salgado
Shawn Hall
Feba Thomas
George E Farmer
Jorge Bermeo
Luis Charles Galindo
Ruben D Ramirez
Santosh D'Mello
Stefan Rose-John
Marco Atzori
The University of Texas at Dallas · USFundar · MXKiel University · DEUniversidad Nacional Autónoma de México · MX

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

backgroundAlthough it is known that stress elevates the levels of pro-inflammatory cytokines and promotes hyper-excitable central conditions, a causal relationship between these two factors has not yet been identified. Recent studies suggest that increases in interleukin 6 (IL-6) levels are specifically associated with stress. We hypothesized that IL-6 acutely and directly induces cortical hyper-excitability by altering the balance between synaptic excitation and inhibition.

methodsWe used patch-clamp to determine the effects of exogenous or endogenous IL-6 on electrically evoked postsynaptic currents on a cortical rat slice preparation. We used control subjects or animals systemically injected with lipopolysaccharide or subjected to electrical foot-shock as rat models of stress.

resultsIn control animals, IL-6 did not affect excitatory postsynaptic currents but selectively and reversibly reduced the amplitude of inhibitory postsynaptic currents with a postsynaptic effect. The IL-6-induced inhibitory postsynaptic currents decrease was inhibited by drugs interfering with receptor trafficking and/or internalization, including wortmannin, Brefeldin A, 2-Br-hexadecanoic acid, or dynamin peptide inhibitor. In both animal models, stress-induced decrease in synaptic inhibition/excitation ratio was prevented by prior intra-ventricular injection of an analog of the endogenous IL-6 trans-signaling blocker gp130.

conclusionsOur results suggest that stress-induced IL-6 shifts the balance between synaptic inhibition and excitation in favor of the latter, possibly by decreasing the density of functional γ-aminobutyric acid A receptors, accelerating their removal and/or decreasing their insertion rate from/to the plasma membrane. We speculate that this mechanism could contribute to stress-induced detrimental long-term increases in central excitability present in a variety of neurological and psychiatric conditions.

Indexed as

AndrostadienesAnimalsBrefeldin ACytokine Receptor gp130Disease Models, AnimalDrug InteractionsElectric StimulationExcitatory Postsynaptic PotentialsInhibitory Postsynaptic PotentialsInterleukin-6Interleukin-6 InhibitorsLipopolysaccharidesMuscimolOligopeptidesPalmitatesRats2-bromopalmitateAndrostadienesBrefeldin ACytokine Receptor gp130Interleukin-6Interleukin-6 InhibitorsLipopolysaccharidesMuscimolOligopeptidesPalmitatespeptide P4Wortmannin

Identifiers

PMID22196984
PMCPMC4732871
OpenAlexW2083811331

What Socratic 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 Socratic graph.