Evidence map›Paper›PMID 23407709›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

D-series resolvin attenuates vascular smooth muscle cell activation and neointimal hyperplasia following vascular injury.

Takuya Miyahara, Sara Runge, Anuran Chatterjee, Mian Chen, Giorgio Mottola, Jonathan M Fitzgerald, Charles N Serhan, Michael S Conte

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02719665 (THE OMEGA-SPM-DOSE and OMEGA-SPM-PAD), which is not on this map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
8.1field-weighted citation impact, top 2% 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.

NCT02719665 nacompletednot on this mapstarted 2016, after this paper: background citation

THE OMEGA-SPM-DOSE and OMEGA-SPM-PAD: Specialized Pro-Resolving Mediators in Patients With Peripheral Artery Disease

TypeinterventionalSponsorUniversity of California, San FranciscoRan2016 to 2020Enrolled30ConditionsPeripheral Arterial Disease, Claudication, Claudication, Intermittent, Vascular OcclusionArmsSPM Emulsion, Dose-modality, SPM Softgel, Dose-Modality, Placebo Softgel
3 · Its place in the literature

Who cites it

91 citing papers in PubMed, 129 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Specialized proresolving lipid mediators in patients with coronary artery disease and their potential for clot remodeling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Review
  9. Review
  10. FPR2 Agonism Attenuates Restenosis by Mitigating Neointimal Hyperplasia via ELOVL6.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  11. Review
  12. Resolvin D2/GPR18 signaling enhances monocytic myeloid-derived suppressor cell function to mitigate abdominal aortic aneurysm formation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Extrinsic and intrinsic modulators of inflammation-resolution signaling in heart failure.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  19. Review
  20. Article

31 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Takuya MiyaharaDivision of Vascular and Endovascular Surgery, University of California-San Francisco, San Francisco, CA 94143-0222, USA.
Sara Runge
Anuran Chatterjee
Mian Chen
Giorgio Mottola
Jonathan M Fitzgerald
Charles N Serhan
Michael S Conte
University of California, San Francisco · USBrigham and Women's Hospital · US

Funding

Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI PETASIS, NICOS A · 2011 to 2020
$14.8M
Genetic Modulation of Vascular Smooth Muscle Phenotype and Intimal HyperplasiaF32HL104851 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUNGE, SARA J · 2010 to 2012
$83k
NHLBI NIH HHS F32 HL104851NHLBI NIH HHS F32 HL 104851-2NIGMS NIH HHS 1P01GM095467NIGMS NIH HHS P01 GM095467
6 · The paper itself

Abstract

Recent evidence suggests that specialized lipid mediators derived from polyunsaturated fatty acids control resolution of inflammation, but little is known about resolution pathways in vascular injury. We sought to determine the actions of D-series resolvin (RvD) on vascular smooth muscle cell (VSMC) phenotype and vascular injury. Human VSMCs were treated with RvD1 and RvD2, and phenotype was assessed by proliferation, migration, monocyte adhesion, superoxide production, and gene expression assays. A rabbit model of arterial angioplasty with local delivery of RvD2 (10 nM vs. vehicle control) was employed to examine effects on vascular injury in vivo. Local generation of proresolving lipid mediators (LC-MS/MS) and expression of RvD receptors in the vessel wall were assessed. RvD1 and RvD2 produced dose-dependent inhibition of VSMC proliferation, migration, monocyte adhesion, superoxide production, and proinflammatory gene expression (IC50≈0.1-1 nM). In balloon-injured rabbit arteries, cell proliferation (51%) and leukocyte recruitment (41%) were reduced at 3 d, and neointimal hyperplasia was attenuated (29%) at 28 d by RvD2. We demonstrate endogenous biosynthesis of proresolving lipid mediators and expression of receptors for RvD1 in the artery wall. RvDs broadly reduce VSMC responses and modulate vascular injury, suggesting that local activation of resolution mechanisms expedites vascular homeostasis.

Indexed as

AnimalsCell AdhesionCell MovementCell ProliferationCells, CulturedDocosahexaenoic AcidsFemoral ArteryHumansInflammation MediatorsMuscle, Smooth, VascularNeointimaRabbitsDocosahexaenoic AcidsInflammation Mediatorsresolvin D1resolvin D2inflammationintracellular signalingresolvin

Identifiers

PMID23407709
PMCPMC3659350
OpenAlexW2055422589

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.