Evidence map›Paper›PMID 18234895›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2008

Targeted disruption of Na+/Ca2+ exchanger 3 (NCX3) gene leads to a worsening of ischemic brain damage.

Pasquale Molinaro, Ornella Cuomo, Giuseppe Pignataro, Francesca Boscia, Rossana Sirabella, Anna Pannaccione, Agnese Secondo, Antonella Scorziello, Annagrazia Adornetto, Rosaria Gala and 6 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008. 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
3.2field-weighted citation impact, top 7% 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, 130 citations in OpenAlex.

  1. Article
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  6. Emerging Role of DREAM in Healthy Brain and Neurological Diseases.International journal of molecular sciences · 2023
    Review
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  10. NaCell communication and signaling : CCS · 2022
    Article
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  14. The NaFrontiers in pharmacology · 2021
    Article
  15. HDAC4 and HDAC5 form a complex with DREAM that epigenetically down-regulates NCX3 gene and its pharmacological inhibition reduces neuronal stroke damage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    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

16 authors at 4 institutions in 3 countries.

Pasquale MolinaroDivision of Pharmacology, Department of Neuroscience, School of Medicine, Federico II University of Naples, 80131 Naples, Italy.
Ornella Cuomo
Giuseppe Pignataro
Francesca Boscia
Rossana Sirabella
Anna Pannaccione
Agnese Secondo
Antonella Scorziello
Annagrazia Adornetto
Rosaria Gala
Davide Viggiano
Sophie Sokolow
Andre Herchuelz
Stèphane Schurmans
Gianfranco Di Renzo
Lucio Annunziato
University of Naples Federico II · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversité Libre de Bruxelles · BEUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Na+/Ca+ exchanger 3 (NCX3), one of the three isoforms of the NCX family, is highly expressed in the brain and is involved in the maintenance of intracellular Na+ and Ca2+ homeostasis. Interestingly, whereas the function of NCX3 under physiological conditions has been determined, its role under anoxia is still unknown. To assess NCX3 role in cerebral ischemia, we exposed ncx3-/- mice to transient middle cerebral artery occlusion followed by reperfusion. In addition, to evaluate the effect of ncx3 ablation on neuronal survival, organotypic hippocampal cultures and primary cortical neurons from ncx3-/- mice were subjected to oxygen glucose deprivation (OGD) plus reoxygenation. Here we report that ncx3 gene suppression leads to a worsening of brain damage after focal ischemia and to a massive neuronal death in all the hippocampal fields of organotypic cultures as well as in cortical neurons from ncx3-/- mice exposed to OGD plus reoxygenation. In addition, in ncx3-/- cortical neurons exposed to hypoxia, NCX currents, recorded in the reverse mode of operation, were significantly lower than those detected in ncx3+/+. From these results, NCX3 protein emerges as a new molecular target that may have a potential therapeutic value in modulating cerebral ischemia.

Indexed as

AnimalsBrain IschemiaCell DeathCell SurvivalDisease ProgressionGene TargetingHippocampusHomeostasisHypoxia, BrainMembrane Transport ProteinsMiceMice, CongenicMice, Inbred C57BLMice, KnockoutNeuronsOrgan Culture TechniquesMembrane Transport ProteinsSlc8a3 protein, mouseSodium-Calcium Exchanger

Identifiers

PMID18234895
PMCPMC6671397
OpenAlexW2028068971

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.