Evidence map›Paper›PMID 33297593›Full record

ArticleInternational journal of molecular sciences2020

Sensitivity of Rodent Microglia to Kynurenines in Models of Epilepsy and Inflammation In Vivo and In Vitro: Microglia Activation is Inhibited by Kynurenic Acid and the Synthetic Analogue SZR104.

Noémi Lajkó, Diana Kata, Melinda Szabó, Adrienne Mátyás, Karolina Dulka, Imre Földesi, Ferenc Fülöp, Karoly Gulya, László Vécsei, András Mihály

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 40% 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, 15 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Noémi LajkóDepartment of Cell Biology and Molecular Medicine, University of Szeged, 6720 Szeged, Hungary.
Diana KataDepartment of Laboratory Medicine, University of Szeged, 6720 Szeged, Hungary.
Melinda SzabóDepartment of Cell Biology and Molecular Medicine, University of Szeged, 6720 Szeged, Hungary.
Adrienne MátyásDepartment of Anatomy, University of Szeged, 6720 Szeged, Hungary.
Karolina DulkaDepartment of Cell Biology and Molecular Medicine, University of Szeged, 6720 Szeged, Hungary.
Imre FöldesiDepartment of Laboratory Medicine, University of Szeged, 6720 Szeged, Hungary.
Ferenc FülöpInstitute of Pharmaceutical Chemistry and Research Group for Stereochemistry, Hungarian Academy of Sciences, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0003-1066-5287
Karoly GulyaDepartment of Cell Biology and Molecular Medicine, University of Szeged, 6720 Szeged, Hungary.
László VécseiDepartment of Neurology, University of Szeged, 6720 Szeged, Hungary.
András MihályDepartment of Anatomy, University of Szeged, 6720 Szeged, Hungary.
University of Szeged · HUCarl von Ossietzky Universität Oldenburg · DE

Funding

Hanse-Wissenschaftskolleg and Oldenburg University gem.§35Abs.2NHGMinistry for Innovation and Technology GINOP 2.3.2-15-2016-00034
6 · The paper itself

Abstract

Kynurenic acid is an endogenous modulator of ionotropic glutamate receptors and a suppressor of the immune system. Since glutamate and microglia are important in the pathogenesis of epilepsy, we investigated the possible action of the synthetic kynurenic acid analogue, SZR104, in epileptic mice and the action of kynurenic acid and SZR104 on the phagocytotic activity of cultured microglia cells. Pilocarpine epilepsy was used to test the effects of SZR104 on morphological microglia transformation, as evaluated through ionized calcium-binding adaptor molecule 1 (Iba1) immunohistochemistry. Microglia-enriched rat secondary cultures were used to investigate phagocytosis of fluorescent microbeads and Iba1 protein synthesis in control and lipopolysaccharide-challenged cultures. SZR104 inhibited microglia transformation following status epilepticus. Kynurenic acid and SZR104 inhibited lipopolysaccharide-stimulated phagocytotic activity of microglia cells. Although kynurenic acid and its analogues proved to be glutamate receptor antagonists, their immunosuppressive action was dominant in epilepsy. The inhibition of phagocytosis in vitro raised the possibility of the inhibition of genes encoding inflammatory cytokines in microglial cells.

Indexed as

AnimalsCalcium-Binding ProteinsCells, CulturedEpilepsyExcitatory Amino Acid AntagonistsKynurenic AcidLipopolysaccharidesMaleMiceMicrofilament ProteinsMicrogliaPhagocytosisPilocarpineAif1 protein, mouseCalcium-Binding ProteinsExcitatory Amino Acid AntagonistsKynurenic AcidLipopolysaccharidesMicrofilament ProteinsPilocarpineepilepsyinflammationkynurenic acidlipopolysaccharidemicrogliapilocarpinesecondary cultureSZR104

Identifiers

PMID33297593
PMCPMC7731372
OpenAlexW3111920824

What OpenQuestion holds

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LicenceCC BY
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.