Evidence map›Paper›PMID 23908248›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2013

Molecular imaging reveals rapid reduction of endothelial activation in early atherosclerosis with apocynin independent of antioxidative properties.

Elham Khanicheh, Yue Qi, Aris Xie, Martina Mitterhuber, Lifen Xu, Michika Mochizuki, Youssef Daali, Vincent Jaquet, Karl-Heinz Krause, Zaverio M Ruggeri and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Molecular Ultrasound Imaging.Nanomaterials (Basel, Switzerland) · 2020
    Review
  6. Article
  7. Article
  8. Ultrasound Molecular Imaging and Drug Delivery.Molecular imaging and biology · 2017
    Review
  9. Article
  10. Molecular Imaging of Vulnerable Atherosclerotic Plaques in Animal Models.International journal of molecular sciences · 2016
    Review
  11. Systems Biology and Noninvasive Imaging of Atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2016
    Review
  12. Review
  13. Ultrasound imaging for risk assessment in atherosclerosis.International journal of molecular sciences · 2015
    Review
  14. Review
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

13 authors at 2 institutions in 2 countries.

Elham KhanichehDivision of Cardiology, Department of Biomedicine, University Hospital and University of Basel, Basel, Switzerland.
Yue Qi
Aris Xie
Martina Mitterhuber
Lifen Xu
Michika Mochizuki
Youssef Daali
Vincent Jaquet
Karl-Heinz Krause
Zaverio M Ruggeri
Gabriela M Kuster
Jonathan R Lindner
Beat A Kaufmann
Oregon Health & Science University · USUniversity Hospital of Geneva · CH

Funding

YR 50 PROJ- ROBERTS PRIMATE ISLETP51RR000163 · NCRR · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI FRUH, KLAUS J · 1985 to 2011
$140.8M
ULTRASOUND IMAGING COREP01HD034430 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI THOMAS, GEORGE VICTOR · 1997 to 2017
$20.7M
Targeted CEU Imaging of Atherosclerosis and AngiogenesisR01HL078610 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2022
$6.8M
Ultrasound Assessment of Microvascular Function in Insulin Resistant PrimatesR01DK063508 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2002 to 2011
$2.7M
STRUCTURE &FUNCTION OF PLATELET MEMBRANE GLYCOPROTEINSR01HL042846 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUGGERI, ZAVERIO M · 1989 to 2014
$2.4M
Contrast-enhanced Ultrasound Assessment of AngiogenesisR01HL074443 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2007
$1.5M
Molecular Imaging of Ischemic Memory with Ultrasound - Transition to HumansRC1HL100659 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LINDNER, JONATHAN R · 2009 to 2010
$979k
NCRR NIH HHS P51 RR000163NHLBI NIH HHS R01 HL042846NHLBI NIH HHS R01 HL074443NHLBI NIH HHS R01 HL078610NHLBI NIH HHS R01-HL-078610NHLBI NIH HHS R01 HL42846NHLBI NIH HHS RC1 HL100659NHLBI NIH HHS RC1-HL-100659NICHD NIH HHS P01 HD034430NIDDK NIH HHS R01 DK063508NIDDK NIH HHS R01-DK-063508
6 · The paper itself

Abstract

objectiveAntioxidative drugs continue to be developed for the treatment of atherosclerosis. Apocynin is an nicotinamide adenine dinucleotide phosphate oxidase inhibitor with anti-inflammatory properties. We used contrast-enhanced ultrasound molecular imaging to assess whether short-term apocynin therapy in atherosclerosis reduces vascular oxidative stress and endothelial activation APPROACH AND

resultsGenetically modified mice with early atherosclerosis were studied at baseline and after 7 days of therapy with apocynin (4 mg/kg per day IP) or saline. Contrast-enhanced ultrasound molecular imaging of the aorta was performed with microbubbles targeted to vascular cell adhesion molecule 1 (VCAM-1; MB(V)), to platelet glycoprotein Ibα (MB(Pl)), and control microbubbles (MB(Ctr)). Aortic vascular cell adhesion molecule 1 was measured using Western blot. Aortic reactive oxygen species generation was measured using a lucigenin assay. Hydroethidine oxidation was used to assess aortic superoxide generation. Baseline signal for MBV (1.3 ± 0.3 AU) and MB(Pl )(1.5 ± 0.5 AU) was higher than for MBCtr (0.5 ± 0.2 AU; P<0.01). In saline-treated animals, signal did not significantly change for any microbubble agent, whereas short-term apocynin significantly (P<0.05) reduced vascular cell adhesion molecule 1 and platelet signal (MBV: 0.3 ± 0.1; MBPl: 0.4 ± 0.1; MBCtr: 0.3 ± 0.2 AU; P=0.6 between agents). Apocynin reduced aortic vascular cell adhesion molecule 1 expression by 50% (P<0.05). However, apocynin therapy did not reduce reactive oxygen species content, superoxide generation, or macrophage content.

conclusionsShort-term treatment with apocynin in atherosclerosis reduces endothelial cell adhesion molecule expression. This change in endothelial phenotype can be detected by molecular imaging before any measurable decrease in macrophage content and is not associated with a detectable change in oxidative burden.

Indexed as

Ultrasonography, InterventionalAcetophenonesAnimalsAnti-Inflammatory AgentsAntioxidantsAortic DiseasesAPOBEC-1 DeaminaseAtherosclerosisBiomarkersBlotting, WesternContrast MediaCytidine DeaminaseDisease Models, AnimalEndothelium, VascularEnzyme InhibitorsMacrophagesAcetophenonesacetovanilloneAnti-Inflammatory AgentsAntioxidantsAPOBEC-1 DeaminaseApobec1 protein, mouseBiomarkersContrast MediaCytidine DeaminaseEnzyme InhibitorsNADPH OxidasesPlatelet Glycoprotein GPIb-IX ComplexReceptors, LDLSuperoxidesVascular Cell Adhesion Molecule-1acetovanilloneatherosclerosismicrobubblesmolecular imagingoxidative stress

Identifiers

PMID23908248
PMCPMC3888901
OpenAlexW2166196920

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.