Evidence map›Paper›PMID 28029679›Full record

ArticleJournal of neurochemistry2017

USP14 inhibitor attenuates cerebral ischemia/reperfusion-induced neuronal injury in mice.

Jia-Wei Min, Lanhai Lü, Jessica L Freeling, Doug S Martin, Hongmin Wang

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
–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

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

5 authors.

Jia-Wei MinDivision of Basic Biomedical Sciences and Center for Brain and Behavior Research, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota, USA.
Lanhai LüGuanghua School of Stomatology, Guangdong Provincial Key Laboratory of Stomatology and Institute of Stomatological Research, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Guangdong, China.
Jessica L FreelingDivision of Basic Biomedical Sciences and Center for Brain and Behavior Research, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota, USA.
Doug S MartinDivision of Basic Biomedical Sciences and Center for Brain and Behavior Research, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota, USA.
Hongmin WangDivision of Basic Biomedical Sciences and Center for Brain and Behavior Research, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota, USA.

Funding

Role of ubiquilin in ischemic strokeR01NS088084 · NINDS · UNIVERSITY OF SOUTH DAKOTA · PI WANG, HONGMIN · 2015 to 2019
$1.4M
Studies of the Therapeutic Role of IU1 in a Mouse Model of Ischemic StrokeR03NS084340 · NINDS · UNIVERSITY OF SOUTH DAKOTA · PI WANG, HONGMIN · 2014 to 2015
$140k
NINDS NIH HHS R01 NS088084NINDS NIH HHS R03 NS084340
6 · The paper itself

Abstract

Stroke is associated with over-production of misfolded and aggregating proteins. However, it remains largely unclear whether enhanced removal of protein aggregates following ischemic stroke is neuroprotective. Deubiquitinating enzymes (DUBs) are a large group of proteases that regulate protein degradation. The ubiquitin-specific protease 14 (USP14) is a DUB that is associated with the proteasome and negatively regulates proteasome activity. In this study, we examined the effect of 1-[1-(4-fluorophenyl)-2,5-dimethylpyrrol-3-yl]-2-pyrrolidin-1-ylethanone (IU1), a specific small molecule inhibitor of USP14, on mouse focal cerebral ischemic stroke-induced neuronal injury in mice. We found that IU1 treatment attenuated ischemic stroke-caused neuronal injury, which was reflected by increased survival rate, reduced infarct volume, as well as decreased neuronal loss in the IU1-treated mice compared to the control-treated mice. Additionally, IU1 treatment is associated with reduced protein aggregates and enhanced proteasome functionality. These data not only highlight the significance of protein homeostasis in cerebral ischemia/reperfusion-induced neuronal injury but also extend the therapeutic role of DUB inhibitors.

Indexed as

AnimalsBehavior, AnimalBrain IschemiaInfarction, Middle Cerebral ArteryMaleMiceMice, Inbred C57BLNeuronsNeuroprotective AgentsProtease InhibitorsProteasome Endopeptidase ComplexPyrrolesPyrrolidinesRecovery of FunctionReperfusion InjurySurvival Analysis1-(1-(4-fluorophenyl)-2,5-dimethylpyrrol-3-yl)-2-pyrrolidin-1-ylethanoneNeuroprotective AgentsProtease InhibitorsProteasome Endopeptidase ComplexPyrrolesPyrrolidinesUbiquitin ThiolesteraseUsp14 protein, mousedeubiquitinating enzymesischemiaIU1small molecule inhibitorstrokeUSP14

Identifiers

PMID28029679
PMCPMC5527549

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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.