Evidence map›Paper›PMID 22042083›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2012

Pentosan polysulfate inhibits atherosclerosis in Watanabe heritable hyperlipidemic rabbits: differential modulation of metalloproteinase-2 and -9.

Enrico Lupia, Feng Zheng, Fabrizio Grosjean, Ivan Tack, Sophie Doublier, Sharon J Elliot, Helen Vlassara, Gary E Striker

Open access · bronzeAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  3. Article
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  5. Article
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  8. Immunomodulatory activity of orphan drug Elmiron® in female B6C3F1/N mice.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2014
    Article
  9. Article
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 6 institutions in 4 countries.

Enrico LupiaDepartment of Geriatrics, Mount Sinai School of Medicine, New York, NY 10029, USA.
Feng Zheng
Fabrizio Grosjean
Ivan Tack
Sophie Doublier
Sharon J Elliot
Helen Vlassara
Gary E Striker
Icahn School of Medicine at Mount Sinai · USFujian Medical University · CNHôpital Rangueil · FRUniversity of Miami · USUniversity of Pavia · ITUniversity of Turin · IT

Funding

Effects of Glycoxidative Stress on Human AgingR01DK091231 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HE, JOHN CIJIANG · 2010 to 2014
$3.1M
NIDDK NIH HHS R01 DK091231
6 · The paper itself

Abstract

Pentosan polysulfate (PPS), a heparinoid compound essentially devoid of anticoagulant activity, modulates cell growth and decreases inflammation. We investigated the effect of PPS on the progression of established atherosclerosis in Watanabe heritable hyperlipidemic (WHHL) rabbits. After severe atherosclerosis developed on an atherogenic diet, WHHL rabbits were treated with oral PPS or tap water for 1 month. The aortic intima-to-media ratio and macrophage infiltration were reduced, plaque collagen content was increased, and plaque fibrous caps were preserved by PPS treatment. Plasma lipid levels and post-heparin hepatic lipase activity remained unchanged. However, net collagenolytic activity in aortic extracts was decreased, and the levels of matrix metalloproteinase (MMP)-2 and tissue inhibitor of metalloproteinase (TIMP) activity were increased by PPS. Moreover, PPS treatment decreased tumor necrosis factor α (TNFα)-stimulated proinflammatory responses, in particular activation of nuclear factor-κB and p38, and activation of MMPs in macrophages. In conclusion, oral PPS treatment prevents progression of established atherosclerosis in WHHL rabbits. This effect may be partially mediated by increased MMP-2 and TIMP activities in the aortic wall and reduced TNFα-stimulated inflammation and MMP activation in macrophages. Thus, PPS may be a useful agent in inhibiting the progression of atherosclerosis.

Indexed as

AnimalsAtherosclerosisCell LineEnzyme ActivationFemaleHumansHyperlipidemiasImmunohistochemistryLipidsMatrix Metalloproteinase 2Matrix Metalloproteinase 9MiceMitogen-Activated Protein KinasesNF-kappa BPentosan Sulfuric PolyesterRabbitsLipidsMatrix Metalloproteinase 2Matrix Metalloproteinase 9Mitogen-Activated Protein KinasesNF-kappa BPentosan Sulfuric PolyesterTumor Necrosis Factor-alpha

Identifiers

PMID22042083
PMCPMC3707145
OpenAlexW2011540524

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.