Evidence map›Paper›PMID 30301943›Full record

ArticleScientific reports2018

Intranasal delivery of a Fas-blocking peptide attenuates Fas-mediated apoptosis in brain ischemia.

Irfan Ullah, Kunho Chung, Jungju Oh, Jagadish Beloor, Sumin Bae, Sangah Clara Lee, Minhyung Lee, Priti Kumar, Sang-Kyung Lee

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Irfan UllahDepartment of Bioengineering and Institute of Nanoscience and Technology, Hanyang University, Seoul, Korea.
Kunho ChungDepartment of Bioengineering and Institute of Nanoscience and Technology, Hanyang University, Seoul, Korea.
Jungju OhDepartment of Bioengineering and Institute of Nanoscience and Technology, Hanyang University, Seoul, Korea.
Jagadish BeloorDepartment of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT, USA.
Sumin BaeDepartment of Bioengineering and Institute of Nanoscience and Technology, Hanyang University, Seoul, Korea.
Sangah Clara LeeDepartment of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT, USA.
Minhyung LeeDepartment of Bioengineering and Institute of Nanoscience and Technology, Hanyang University, Seoul, Korea.
Priti KumarDepartment of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT, USA. priti.kumar@yale.edu.
Sang-Kyung LeeDepartment of Bioengineering and Institute of Nanoscience and Technology, Hanyang University, Seoul, Korea. sangkyunglee@hanyang.ac.kr.
Hanyang University · KRYale University · USBrown University · US

Funding

In vivo genomic editing of hematopoietic cells for HIV resistanceR01AI112443 · NIAID · YALE UNIVERSITY · PI GLAZER, PETER M, KUMAR, PRITI · 2014 to 2017
$2.1M
National Research Foundation of Korea (NRF) 2017R1D1A1B03029636NIAID NIH HHS R01 AI112443U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AI112443
6 · The paper itself

Abstract

Ischemic stroke-induced neuronal cell death results in the permanent disabling of brain function. Apoptotic mechanisms are thought to play a prominent role in neuronal injury and ample evidence implicates Fas signaling in mediating cell death. In this study, we describe the neuroprotective effects of a Fas-blocking peptide (FBP) that by obstructing Fas signaling in cerebral ischemia inhibits apoptosis. Using an intranasal administration route in a rat model of focal cerebral ischemia, we demonstrate that nose-to-brain delivery of FBP after middle cerebral artery occlusion (MCAO) surgery results in the delivery and retention of FBP in Fas-expressing ischemic areas of the brain. A single intranasal administration of 2 mg/kg FBP resulted in significantly reduced neuronal cell death by inhibiting Fas-mediated apoptosis leading to decreased infarct volumes, reduced neurologic deficit scores and recovery from cerebral ischemia. Intranasally delivered FBP might be a promising strategy for the treatment of cerebral ischemic stroke.

Indexed as

AnimalsApoptosisBiomarkersBrainBrain IschemiaCell Linefas ReceptorHumansImmunohistochemistryMicePeptidesRatsBiomarkersfas ReceptorPeptides

Identifiers

PMID30301943
PMCPMC6178348
OpenAlexW2895047553

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.