Evidence map›Paper›PMID 23956444›Full record

ArticleJournal of lipid research2013

Inhibition of myeloperoxidase decreases vascular oxidative stress and increases vasodilatation in sickle cell disease mice.

Hao Zhang, Hao Xu, Dorothee Weihrauch, Deron W Jones, Xigang Jing, Yang Shi, David Gourlay, Keith T Oldham, Cheryl A Hillery, Kirkwood A Pritchard

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

34 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. Phytochemical Characterization ofMolecules (Basel, Switzerland) · 2025
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Myeloperoxidase instigates proinflammatory responses in a cecal ligation and puncture rat model of sepsis.American journal of physiology. Heart and circulatory physiology · 2020
    Article
  18. Article
  19. Article
  20. 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

10 authors at 2 institutions in 1 country.

Hao ZhangDepartments of Surgery, Milwaukee, WI 53226.
Hao Xu
Dorothee Weihrauch
Deron W Jones
Xigang Jing
Yang Shi
David Gourlay
Keith T Oldham
Cheryl A Hillery
Kirkwood A Pritchard
Aurora Health Care · USVersiti Blood Center of Wisconsin · US

Funding

Mechanisms of Inflammation in Sickle Cell DiseaseR01HL128371 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI PRITCHARD, KIRKWOOD ARTHUR · 2016 to 2024
$4.2M
Sickle Cell ScholarU54HL090503 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HILLERY, CHERYL A · 2008 to 2011
$3.0M
Biophysics of HDL DysfunctionR01HL112270 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI PRITCHARD, KIRKWOOD ARTHUR, SORCI-THOMAS, MARY G · 2012 to 2015
$2.5M
Inflammation, fibrosis and myocardial function in schlerodermaR01HL089779 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI WEIHRAUCH, DOROTHEE · 2008 to 2012
$2.2M
Asthma Increases Vaso-occlusion in Sickle Cell DiseaseR01HL102836 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HILLERY, CHERYL A, PRITCHARD, KIRKWOOD ARTHUR · 2010 to 2013
$2.2M
Hsp90, NOS3 and CardioprotectionR01HL080468 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI SHI, YANG · 2006 to 2009
$1.7M
Novel Peptide MPO Inhibitors for Treating AtherosclerosisR21HL102996 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI PRITCHARD, KIRKWOOD ARTHUR · 2011 to 2012
$413k
NHLBI NIH HHS HL-080468SNHLBI NIH HHS HL-089779NHLBI NIH HHS HL-102836NHLBI NIH HHS HL-102996NHLBI NIH HHS R01 HL080468NHLBI NIH HHS R01 HL089779NHLBI NIH HHS R01 HL102836NHLBI NIH HHS R01 HL112270NHLBI NIH HHS R01 HL128371NHLBI NIH HHS R21 HL102996NHLBI NIH HHS U54 HL-090503NHLBI NIH HHS U54 HL090503
6 · The paper itself

Abstract

Activated leukocytes and polymorphonuclear neutrophils (PMN) release myeloperoxidase (MPO), which binds to endothelial cells (EC), is translocated, and generates oxidants that scavenge nitric oxide (NO) and impair EC function. To determine whether MPO impairs EC function in sickle cell disease (SCD), control (AA) and SCD mice were treated with N-acetyl-lysyltyrosylcysteine-amide (KYC). SCD humans and mice have high plasma MPO and soluble L-selectin (sL-selectin). KYC had no effect on MPO but decreased plasma sL-selectin and malondialdehyde in SCD mice. MPO and 3-chlorotyrosine (3-ClTyr) were increased in SCD aortas. KYC decreased MPO and 3-ClTyr in SCD aortas to the levels in AA aortas. Vasodilatation in SCD mice was impaired. KYC increased vasodilatation in SCD mice more than 2-fold, to ∼60% of levels in AA mice. KYC inhibited MPO-dependent 3-ClTyr formation in EC proteins. SCD mice had high plasma alanine transaminase (ALT), which tended to decrease in KYC-treated SCD mice (P = 0.07). KYC increased MPO and XO/XDH and decreased 3-ClTyr and 3-nitrotyrosine (3-NO₂Tyr) in SCD livers. These data support the hypothesis that SCD increases release of MPO, which generates oxidants that impair EC function and injure livers. Inhibiting MPO is an effective strategy for decreasing oxidative stress and liver injury and restoring EC function in SCD.

Indexed as

Anemia, Sickle CellAnimalsBlood VesselsDose-Response Relationship, DrugEndothelial CellsEnzyme InhibitorsFemaleHumansHypochlorous AcidLiverL-SelectinMaleMiceOligopeptidesOxidative StressPeroxidaseEnzyme InhibitorsHypochlorous AcidL-SelectinOligopeptidesPeroxidaseaortachlorotyrosineendothelial cellsfacialis arteryliverL-selectinmalondialdehydepolymorphonuclear cells

Identifiers

PMID23956444
PMCPMC3793605
OpenAlexW2125519973

What OpenQuestion holds

Textmetadata
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.