Evidence map›Paper›PMID 28888095›Full record

ArticleBritish journal of pharmacology2017

Magnesium therapy improves outcome in Streptococcus pneumoniae meningitis by altering pneumolysin pore formation.

Sabrina Hupp, Sandra Ribes, Jana Seele, Carolin Bischoff, Christina Förtsch, Elke Maier, Roland Benz, Timothy J Mitchell, Roland Nau, Asparouh I Iliev

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 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 4 institutions in 3 countries.

Sabrina HuppInstitute of Anatomy, University of Bern, Bern, Switzerland.
Sandra RibesDepartment of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Jana SeeleDepartment of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Carolin BischoffDFG Membrane/Cytoskeleton Interaction Group, Institute of Pharmacology and Toxicology & Rudolf Virchow Center for Experimental Medicine, University of Würzburg, Würzburg, Germany.
Christina FörtschDFG Membrane/Cytoskeleton Interaction Group, Institute of Pharmacology and Toxicology & Rudolf Virchow Center for Experimental Medicine, University of Würzburg, Würzburg, Germany.
Elke MaierRudolf Virchow Center for Experimental Medicine, University of Würzburg, Würzburg, Germany.
Roland BenzRudolf Virchow Center for Experimental Medicine, University of Würzburg, Würzburg, Germany.
Timothy J MitchellInstitute of Microbiology and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Roland NauDepartment of Neuropathology, University Medical Center Göttingen, Göttingen, Germany.
Asparouh I IlievInstitute of Anatomy, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0002-1343-2967
University of Würzburg · DEUniversitätsmedizin Göttingen · DEUniversity of Bern · CHUniversity of Birmingham · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

background and purposeStreptococcus pneumoniae is the most common cause of bacterial meningitis in adults and is characterized by high lethality and substantial cognitive disabilities in survivors. Here, we have studied the capacity of an established therapeutic agent, magnesium, to improve survival in pneumococcal meningitis by modulating the neurological effects of the major pneumococcal pathogenic factor, pneumolysin. EXPERIMENTAL APPROACH: We used mixed primary glial and acute brain slice cultures, pneumolysin injection in infant rats, a mouse meningitis model and complementary approaches such as Western blot, a black lipid bilayer conductance assay and live imaging of primary glial cells. KEY

resultsTreatment with therapeutic concentrations of magnesium chloride (500 mg·kg CONCLUSIONS AND IMPLICATIONS: Magnesium is a well-established and safe therapeutic agent that has demonstrated capacity for attenuating pneumolysin-triggered pathogenic effects on the brain. The improved animal survival and clinical condition in the meningitis model identifies magnesium as a promising candidate for adjunctive treatment of pneumococcal meningitis, together with antibiotic therapy.

Indexed as

AnimalsBacterial ProteinsBrainDisease Models, AnimalFemaleMagnesium ChlorideMeningitis, PneumococcalMiceMice, Inbred C57BLNeurogliaRatsRats, Sprague-DawleyStreptococcus pneumoniaeStreptolysinsSurvival RateBacterial ProteinsMagnesium ChlorideplY protein, Streptococcus pneumoniaeStreptolysins

Identifiers

PMID28888095
PMCPMC5715590
OpenAlexW2750741543

What OpenQuestion holds

Textmetadata
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.