Evidence map›Paper›PMID 26539914›Full record

ArticleCell death & disease2015

Targeting caspase-6 and caspase-8 to promote neuronal survival following ischemic stroke.

A P Shabanzadeh, P M D'Onofrio, P P Monnier, P D Koeberle

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.3field-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

39 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
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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

4 authors at 2 institutions in 1 country.

A P ShabanzadehDivision of Anatomy, Department of Surgery, University of Toronto, Toronto, Canada.
P M D'OnofrioDivision of Anatomy, Department of Surgery, University of Toronto, Toronto, Canada.
P P MonnierToronto Western Research Institute, Toronto Western Hospital, Toronto, Canada.
P D KoeberleDivision of Anatomy, Department of Surgery, University of Toronto, Toronto, Canada.
University of Toronto · CAToronto Western Hospital · CA

Funding

Canadian Institutes of Health Research MOP106666Canadian Institutes of Health Research MOP 119309
6 · The paper itself

Abstract

Previous studies show that caspase-6 and caspase-8 are involved in neuronal apoptosis and regenerative failure after trauma of the adult central nervous system (CNS). In this study, we evaluated whether caspase-6 or -8 inhibitors can reduce cerebral or retinal injury after ischemia. Cerebral infarct volume, relative to appropriate controls, was significantly reduced in groups treated with caspase-6 or -8 inhibitors. Concomitantly, these treatments also reduced neurological deficits, reduced edema, increased cell proliferation, and increased neurofilament levels in the injured cerebrum. Caspase-6 and -8 inhibitors, or siRNAs, also increased retinal ganglion cell survival at 14 days after ischemic injury. Caspase-6 or -8 inhibition also decreased caspase-3, -6, and caspase-8 cleavage when assayed by western blot and reduced caspase-3 and -6 activities in colorimetric assays. We have shown that caspase-6 or caspase-8 inhibition decreases the neuropathological consequences of cerebral or retinal infarction, thereby emphasizing their importance in ischemic neuronal degeneration. As such, caspase-6 and -8 are potential targets for future therapies aimed at attenuating the devastating functional losses that result from retinal or cerebral stroke.

Indexed as

AnimalsApoptosisCaspase 6Caspase 8Caspase InhibitorsFemaleMolecular Targeted TherapyNeuronsNeuroprotective AgentsRatsRats, Sprague-DawleyReperfusion InjuryRetinaStrokeCaspase 6Caspase 8Caspase InhibitorsNeuroprotective Agents

Identifiers

PMID26539914
PMCPMC4670918
OpenAlexW1904500917

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.