Evidence map›Paper›PMID 39075243›Full record

ArticleIn vitro cellular & developmental biology. Animal2024

Protection from oxygen-glucose deprivation by neurosteroid treatment in primary neurons and oligodendrocytes.

Roisin Moloney, Carlton L Pavy, Richard G S Kahl, Hannah K Palliser, Jon J Hirst, Julia C Shaw

Abstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Roisin MoloneySchool of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia. roisin.moloney@uon.edu.au.ORCID http://orcid.org/0000-0003-1373-6781
Carlton L PavySchool of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia.
Richard G S KahlSchool of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia.
Hannah K PalliserSchool of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia.
Jon J HirstSchool of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia.
Julia C ShawSchool of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preterm birth results in an increased risk of neonatal brain injury and neurobehavioural disorders. Despite the seriousness of these adverse outcomes, there are currently no effective therapies to protect the vulnerable developing brain. We propose that neurosteroid replacement therapy may be a novel approach in reducing detrimental neurological outcomes following preterm birth. The use of guinea pig primary neuronal and oligodendrocyte cultures with relevance to late gestation allows insight into the mechanisms behind the effectiveness of these treatments. Primary neuronal and oligodendrocyte cultures were derived from fetal guinea pig frontal cortex brain tissue at gestational age 62 (GA62). Cell cultures were pre-treated with either etifoxine (5 µM) or zuranolone (1 µm) for 24 h prior to insult. Cells were then exposed to either oxygen-glucose deprivation (OGD; 0% O

Indexed as

GlucoseNeuronsNeurosteroidsOligodendrogliaOxygenAnimalsCell HypoxiaCells, CulturedGuinea PigsNeuroprotective AgentsGlucoseNeuroprotective AgentsNeurosteroidsOxygenGABANeuronNeurosteroidOligodendrocytePreterm birth

Identifiers

PMID39075243
PMCPMC11534971

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.