Evidence map›Paper›PMID 25275601›Full record

ArticleCell death & disease2014

Seizure activity results in calcium- and mitochondria-independent ROS production via NADPH and xanthine oxidase activation.

S Kovac, A-M Domijan, M C Walker, A Y Abramov

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 146 citations in OpenAlex.

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11 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 2 countries.

S Kovac1] UCL Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK [2] Department of Neurology, University of Muenster, Muenster 48149, Germany.
A-M DomijanFaculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb 10000, Croatia.
M C WalkerUCL Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.
A Y AbramovUCL Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.
University College London · GBNational Hospital for Neurology and Neurosurgery · GBUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seizure activity has been proposed to result in the generation of reactive oxygen species (ROS), which then contribute to seizure-induced neuronal damage and eventually cell death. Although the mechanisms of seizure-induced ROS generation are unclear, mitochondria and cellular calcium overload have been proposed to have a crucial role. We aim to determine the sources of seizure-induced ROS and their contribution to seizure-induced cell death. Using live cell imaging techniques in glioneuronal cultures, we show that prolonged seizure-like activity increases ROS production in an NMDA receptor-dependent manner. Unexpectedly, however, mitochondria did not contribute to ROS production during seizure-like activity. ROS were generated primarily by NADPH oxidase and later by xanthine oxidase (XO) activity in a calcium-independent manner. This calcium-independent neuronal ROS production was accompanied by an increase in intracellular [Na(+)] through NMDA receptor activation. Inhibition of NADPH or XO markedly reduced seizure-like activity-induced neuronal apoptosis. These findings demonstrate a critical role for ROS in seizure-induced neuronal cell death and identify novel therapeutic targets.

Indexed as

AnimalsApoptosisCalciumHumansMitochondriaNADPNADPH OxidasesNeuronsOxidative StressRatsRats, Sprague-DawleyReactive Oxygen SpeciesReceptors, N-Methyl-D-AspartateSeizuresSodiumXanthine OxidaseCalciumNADPNADPH OxidasesReactive Oxygen SpeciesReceptors, N-Methyl-D-AspartateSodiumXanthine Oxidase

Identifiers

PMID25275601
PMCPMC4649505
OpenAlexW1972959301

What OpenQuestion holds

Textmetadata
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.