Evidence map›Paper›PMID 27132231›Full record

ArticleNeuroscience2016

Inhibition of cerebral vascular inflammation by brain endothelium-targeted oligodeoxynucleotide complex.

Jing Hu, Daniah Al-Waili, Aishlin Hassan, Guo-Chang Fan, Mei Xin, Jiukuan Hao

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 10 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

6 authors at 3 institutions in 1 country.

Jing HuDivision of Pharmaceutical Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267, USA.
Daniah Al-WailiDivision of Pharmaceutical Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267, USA.
Aishlin HassanDepartment of Pediatrics, University of Cincinnati & Cincinnati Children's Hospital Medical Center, USA.
Guo-Chang FanDepartment of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Mei XinDepartment of Pediatrics, University of Cincinnati & Cincinnati Children's Hospital Medical Center, USA.
Jiukuan HaoDivision of Pharmaceutical Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267, USA. Electronic address: haojn@ucmail.uc.edu.
University of Cincinnati Medical Center · USCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · US

Funding

Roles of Hsp20-Exosomes in Myocardial AngiogenesisR01HL087861 · NHLBI · UNIVERSITY OF CINCINNATI · PI FAN, GUO-CHANG · 2007 to 2017
$4.2M
Duplex miR-223 and Exosomes in SepsisR01GM112930 · NIGMS · UNIVERSITY OF CINCINNATI · PI FAN, GUO-CHANG · 2015 to 2018
$1.2M
Targeting the Blood-Brain Barrier in Ischemic StrokeR15NS088384 · NINDS · UNIVERSITY OF CINCINNATI · PI HAO, JIUKUAN · 2015 to 2015
$487k
Application of Brain-Targeted Anti-inflammatory RNA Nanoparticle for Ischemic Stroke TherapyR21NS093493 · NINDS · UNIVERSITY OF CINCINNATI · PI HAO, JIUKUAN · 2015 to 2016
$448k
NHLBI NIH HHS R01 HL087861NIGMS NIH HHS R01 GM112930NINDS NIH HHS R15 NS088384NINDS NIH HHS R21 NS093493
6 · The paper itself

Abstract

The present study generated a novel DNA complex to specifically target endothelial NF-κB to inhibit cerebral vascular inflammation. This DNA complex (GS24-NFκB) contains a DNA decoy which inhibits NF-κB activity, and a DNA aptamer (GS-24), a ligand of transferrin receptor (TfR), which allows for targeted delivery of the DNA decoy into cells. The results indicate that GS24-NFκB was successfully delivered into a murine brain-derived endothelial cell line, bEND5, and inhibited inflammatory responses induced by tumor necrosis factor α (TNF-α) or oxygen-glucose deprivation/re-oxygenation (OGD/R) via down-regulation of the nuclear NF-κB subunit, p65, as well as its downstream inflammatory cytokines, inter-cellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule (VCAM-1). The inhibitory effect of the GS24-NFκB was demonstrated by a significant reduction in TNF-α or OGD/R induced monocyte adhesion to the bEND5 cells after GS24-NFκB treatment. Intravenous (i.v.) injection of GS24-'NFκB (15mg/kg) was able to inhibit the levels of phoseph-p65 and VCAM-1 in brain endothelial cells in a mouse lipopolysaccharide (LPS)-induced inflammatory model in vivo. In conclusion, our approach using DNA nanotechnology for DNA decoy delivery could potentially be utilized for inhibition of inflammation in ischemic stroke and other neuro-inflammatory diseases affecting cerebral vasculature.

Indexed as

AnimalsAnti-Inflammatory AgentsAptamers, NucleotideBrainCell HypoxiaCell LineDisease Models, AnimalDrug DesignDrug Evaluation, PreclinicalEndothelial CellsGlucoseGoatsInflammationLipopolysaccharidesMaleMiceAnti-Inflammatory AgentsAptamers, NucleotideGlucoseLipopolysaccharidesNeuroprotective AgentsOligodeoxyribonucleotidesTumor Necrosis Factor-alphaaptamerendothelial cellsinflammationlipopolysaccharideNF-κBoxygen-glucose deprivation

Identifiers

PMID27132231
PMCPMC4905813
OpenAlexW2345731209

What OpenQuestion holds

Textmetadata
LicenceTDM
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.