Evidence map›Paper›PMID 21183734›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2011

A modified sesamol derivative inhibits progression of atherosclerosis.

Zhekang Ying, Nisharahmed Kherada, Thomas Kampfrath, Georgeta Mihai, Orlando Simonetti, Rajagopal Desikan, Karuppaiyah Selvendiran, Qinghua Sun, Ouiliana Ziouzenkova, Sampath Parthasarathy and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 40 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

11 authors at 1 institution in 1 country.

Zhekang YingDavis Heart Lung Research Institute, Ohio State University, Columbus, OH 43210-1252, USA.
Nisharahmed Kherada
Thomas Kampfrath
Georgeta Mihai
Orlando Simonetti
Rajagopal Desikan
Karuppaiyah Selvendiran
Qinghua Sun
Ouiliana Ziouzenkova
Sampath Parthasarathy
Sanjay Rajagopalan
Q Therapeutics (United States) · US

Funding

Air Pollution and Hypertension: Vascular MechanismsR01ES015146 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI RAJAGOPALAN, SANJAY · 2007 to 2018
$4.5M
Diet-Environment Interactions in InflammationR01ES017290 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI RAJAGOPALAN, SANJAY · 2010 to 2014
$1.8M
Air Pollution Exposure/Atherosclerosis:Vascular MechanismR01ES013406 · NIEHS · OHIO STATE UNIVERSITY · PI RAJAGOPALAN, SANJAY · 2004 to 2007
$1.3M
T Regulatory Cells as Determinants of Inflammation in Adipose TissueR21DK088522 · NIDDK · OHIO STATE UNIVERSITY · PI RAJAGOPALAN, SANJAY · 2010 to 2011
$417k
NIDDK NIH HHS R21 DK088522NIEHS NIH HHS ES017290NIEHS NIH HHS R01 ES013406NIEHS NIH HHS R01 ES015146NIEHS NIH HHS R01 ES017290
6 · The paper itself

Abstract

objectiveSesamol, a phenolic component of lignans, has been previously shown to reduce lipopolysaccharide-induced oxidative stress and upregulate phosphatidylinositol 3-kinase/Akt/endothelial nitric oxide synthase pathways. In the present study, we synthesized a modified form of sesamol (INV-403) to enhance its properties and assessed its effects on atherosclerosis. METHODS AND

resultsWatanabe heritable hyperlipidemic rabbits were fed with high-cholesterol chow for 6 weeks and then randomized to receive high-cholesterol diet either alone or combined with INV-403 (20 mg/kg per day) for 12 weeks. Serial MRI analysis demonstrated that INV-403 rapidly reduced atherosclerotic plaques (within 6 weeks), with confirmatory morphological analysis at 12 weeks posttreatment revealing reduced atherosclerosis paralleled by reduction in lipid and inflammatory cell content. Consistent with its effect on atherosclerosis, INV-403 improved vascular function (decreased constriction to angiotensin II and increased relaxation to acetylcholine), reduced systemic and plaque oxidative stress, and inhibited nuclear factor-κB activation via effects on nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (IκBα) phosphorylation with coordinate reduction in key endothelial adhesion molecules. In vitro experiments in cultured endothelial cells revealed effects of INV-403 in reducing IκBα phosphorylation via inhibition of IκB kinase 2 (IKK2).

conclusionsINV-403 is a novel modified lignan derivative that potently inhibits atherosclerosis progression via its effects on IKK2 and nuclear factor-κB signaling.

Indexed as

AnimalsAortaAortic DiseasesAtherosclerosisBenzodioxolesCardiovascular AgentsCattleCell Adhesion MoleculesCells, CulturedDisease Models, AnimalDose-Response Relationship, DrugEndothelial CellsGene Expression RegulationHyperlipidemiasI-kappa B KinaseI-kappa B ProteinsBenzodioxolesCardiovascular AgentsCell Adhesion MoleculesI-kappa B KinaseI-kappa B ProteinsNF-kappa BNF-KappaB Inhibitor alphaPhenolssesamol

Identifiers

PMID21183734
PMCPMC5343762
OpenAlexW2121628963

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.