Evidence map›Paper›PMID 26691164›Full record

ArticleTranslational stroke research2016

Acute Blockage of Notch Signaling by DAPT Induces Neuroprotection and Neurogenesis in the Neonatal Rat Brain After Stroke.

Zhongxia Li, Jiangping Wang, Congying Zhao, Keming Ren, Zhezhi Xia, Huimin Yu, Kewen Jiang

Abstract read
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In one paragraph

Article in Translational stroke research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
10.3field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

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  17. Rehabilitation and the Neural Network After Stroke.Translational stroke research · 2017
    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

7 authors at 1 institution in 1 country.

Zhongxia LiDepartment of Laboratory, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China.
Jiangping WangDepartment of Rehabilitation, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China.
Congying ZhaoDepartment of Laboratory, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China.
Keming RenDepartment of Laboratory, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China.
Zhezhi XiaDepartment of Neurology, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China.
Huimin YuDepartment of Neonatology, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China.
Kewen JiangDepartment of Laboratory, The Children's Hospital Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310003, China. jiangkw_zju@163.com.
Children's Hospital of Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Notch signaling is critically involved in various biological events. Notch undergoes cleavage by the γ-secretase enzyme to release Notch intracellular domain that will translocate into nucleus to result in expression of target gene. γ-Secretase inhibitors have been developed as potential treatments for neurological degenerative diseases, but its effects against ischemic injury remain relatively uncertain. In the present study, we demonstrated that N-[N-(3, 5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester (DAPT), a γ-secretase inhibitor not only rescued the cerebral hypoperfusion or ischemia neonatal rats from death, reduced apoptosis in penumbra, but also reduced brain infarct size. Furthermore, DAPT elicited some morphologic hallmarks such as neurogenesis and angiogenesis that related to the brain repair and functional recovery after stroke: increased accumulations of newborn cells in the peri-infarct region with a higher fraction of them adopting immature neuronal and glial markers instead of microglial markers on 5 days, enhanced vascular densities in penumbra at 14 days, and evident regulations of the gene profiles associated with neurogenesis in penumbral tissues. The current results suggest that DAPT is a potential neuroprotectants against ischemic injury in immature brain, and future treatment strategies such as clinical trials using γ-secretase inhibitors would be an attractive therapy for perinatal ischemia.

Indexed as

StrokeAnimalsAnimals, NewbornBrain InfarctionDiaminesDisease Models, AnimalGene Expression ProfilingGene Expression RegulationIn Situ Nick-End LabelingMaleNeurogenesisNeuroprotective AgentsOligonucleotide Array Sequence AnalysisRatsRats, Sprague-DawleyReceptors, Notch24-diamino-5-phenylthiazoleDiaminesNeuroprotective AgentsReceptors, NotchRNA, MessengerThiazolesAngiogenesisIschemiaNeurogenesisNeuroprotectionN-[N-(3, 5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl esterNotch signaling

Identifiers

PMID26691164
OpenAlexW2211687367

What OpenQuestion holds

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Registered trials

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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.