Evidence map›Paper›PMID 25032854›Full record

ArticleCell death & disease2014

Ischemic tolerance modulates TRAIL expression and its receptors and generates a neuroprotected phenotype.

G Cantarella, G Pignataro, G Di Benedetto, S Anzilotti, A Vinciguerra, O Cuomo, G F Di Renzo, C Parenti, L Annunziato, R Bernardini

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 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. TRAIL-R Deficient Mice Are Protected from Neurotoxic Effects of Amyloid-β.International journal of molecular sciences · 2022
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. The immune system on the TRAIL of Alzheimer's disease.Journal of neuroinflammation · 2020
    Review
  17. Review
  18. HIF-1α Mediates TRAIL-Induced Neuronal ApoptosisFrontiers in cellular neuroscience · 2020
    Article
  19. Article
  20. 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

10 authors at 3 institutions in 1 country.

G CantarellaDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, School of Medicine, University of Catania, Viale Andrea Doria-6, Catania, Italy.
G PignataroDepartment of Neuroscience, Division of Pharmacology, School of Medicine, Federico II University of Naples, Via Pansini, 5, Naples, Italy.
G Di BenedettoDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, School of Medicine, University of Catania, Viale Andrea Doria-6, Catania, Italy.
S AnzilottiFondazione IRCCS SDN, Via Gianturco, Naples, Italy.
A VinciguerraDepartment of Neuroscience, Division of Pharmacology, School of Medicine, Federico II University of Naples, Via Pansini, 5, Naples, Italy.
O CuomoDepartment of Neuroscience, Division of Pharmacology, School of Medicine, Federico II University of Naples, Via Pansini, 5, Naples, Italy.
G F Di RenzoDepartment of Neuroscience, Division of Pharmacology, School of Medicine, Federico II University of Naples, Via Pansini, 5, Naples, Italy.
C ParentiDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Catania, Catania, Italy.
L Annunziato1] Department of Neuroscience, Division of Pharmacology, School of Medicine, Federico II University of Naples, Via Pansini, 5, Naples, Italy [2] Fondazione IRCCS SDN, Via Gianturco, Naples, Italy.
R BernardiniDepartment of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, School of Medicine, University of Catania, Viale Andrea Doria-6, Catania, Italy.
University of Catania · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITSDN Istituto di Ricerca Diagnostica e Nucleare · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TNF-related apoptosis inducing ligand (TRAIL), a member of the TNF superfamily released by microglia, appears to be involved in the induction of apoptosis following focal brain ischemia. Indeed, brain ischemia is associated with progressive enlargement of damaged areas and prominent inflammation. As ischemic preconditioning reduces inflammatory response to brain ischemia and ameliorates brain damage, the purpose of the present study was to evaluate the role of TRAIL and its receptors in stroke and ischemic preconditioning and to propose, by modulating TRAIL pathway, a new therapeutic strategy in stroke. In order to achieve this aim a rat model of harmful focal ischemia, obtained by subjecting animals to 100 min of transient occlusion of middle cerebral artery followed by 24 h of reperfusion and a rat model of ischemic preconditioning in which the harmful ischemia was preceded by 30 mins of tMCAO, which represents the preconditioning protective stimulus, were used. Results show that the neuroprotection elicited by ischemic preconditioning occurs through both upregulation of TRAIL decoy receptors and downregulation of TRAIL itself and of its death receptors. As a counterproof, immunoneutralization of TRAIL in tMCAO animals resulted in significant restraint of tissue damage and in a marked functional recovery. Our data shed new light on the mechanisms that propagate ongoing neuronal damage after ischemia in the adult mammalian brain and provide new molecular targets for therapeutic intervention. Strategies aimed to repress the death-inducing ligands TRAIL, to antagonize the death receptors, or to activate the decoy receptors open new perspectives for the treatment of stroke.

Indexed as

AnimalsBrain IschemiaGene Expression RegulationHumansIschemic PreconditioningMaleNeuronsRatsRats, Sprague-DawleyReceptors, TNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing LigandReceptors, TNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing Ligand

Identifiers

PMID25032854
PMCPMC4123080
OpenAlexW1987482729

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.