Evidence map›Paper›PMID 19342499›Full record

ArticleJournal of cardiovascular pharmacology and therapeutics2009

The cyclic GMP modulators YC-1 and zaprinast reduce vessel remodeling through antiproliferative and proapoptotic effects.

Amit N Keswani, Kelly J Peyton, William Durante, Andrew I Schafer, David A Tulis

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of cardiovascular pharmacology and therapeutics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Deleterious effects of phosphate on vascular and endothelial function via disruption to the nitric oxide pathway.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    Article
  4. Article
  5. Article
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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

5 authors at 4 institutions in 1 country.

Amit N KeswaniDepartment of Internal Medicine, University of Texas Medical Branch, Galveston, Texas, USA.
Kelly J Peyton
William Durante
Andrew I Schafer
David A Tulis
University of Missouri · USCornell University · USEast Carolina University · USThe University of Texas Medical Branch at Galveston · US

Funding

CARBON MONOXIDE AND VASCULAR SMOOTH MUSCLE CELL FUNCTIONR01HL059976 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI DURANTE, WILLIAM · 1999 to 2013
$3.3M
CARDIOVASCULAR HEALTH AMONG AFRICAN AMERICANSUH1HL059868 · NHLBI · NORTH CAROLINA CENTRAL UNIVERSITY · PI HAREWOOD, KEN RUPERT · 1997 to 2004
$2.5M
NO-independent cGMP regulation of vascular remodelingR01HL081720 · NHLBI · NORTH CAROLINA CENTRAL UNIVERSITY · PI TULIS, DAVID A · 2007 to 2012
$2.2M
REGULATION OF PLATELET/ENDOTHELIAL INTERACTIONSR01HL036045 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SCHAFER, ANDREW I · 1985 to 2006
$2.1M
Cardiovascular Health Among African AmericansR25HL059868 · NHLBI · NORTH CAROLINA CENTRAL UNIVERSITY · PI KIMBRO, KEVIN SEAN · 2006 to 2010
$1.7M
VASCULAR CELL CATIONIC AMINO ACID TRANSPORT &METABOLISMR01HL062467 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI SCHAFER, ANDREW I · 1999 to 2002
$926k
NHLBI NIH HHS HL-36045NHLBI NIH HHS HL-59868NHLBI NIH HHS HL-59976NHLBI NIH HHS HL-62467NHLBI NIH HHS HL-81720NHLBI NIH HHS R01 HL036045NHLBI NIH HHS R01 HL059976NHLBI NIH HHS R01 HL081720NHLBI NIH HHS R25 HL059868NHLBI NIH HHS UH1 HL059868
6 · The paper itself

Abstract

Guanosine-specific cyclic nucleotide signaling is suggested to serve protective actions in the vasculature; however, the influence of selective pharmacologic modulation of cyclic guanosine monophosphate- synthesizing soluble guanylate cyclase or cyclic guanosine monophosphate-degrading phosphodiesterase on vessel remodeling has not been thoroughly examined. In this study, rat carotid artery balloon injury was performed and the growth-modulating effects of the soluble guanylate cyclase stimulator YC-1 or the cyclic guanosine monophosphate-dependent phosphodiesterase-V inhibitor zaprinast were examined. YC-1 or zaprinast elevated vessel cyclic guanosine monophosphate content, reduced medial wall and neointimal cell proliferation, stimulated medial and neointimal cellular apoptosis, and markedly attenuated neointimal remodeling in comparable fashion. Interestingly, soluble guanylate cyclase inhibition by 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one failed to noticeably alter neointimal growth, and concomitant zaprinast with YC-1 did not modify any parameter compared to individual treatments. These results provide novel in vivo evidence that YC-1 and zaprinast inhibit injury-induced vascular remodeling through antimitogenic and proapoptotic actions and may offer promising therapeutic approaches against vasoproliferative disorders.

Indexed as

AnimalsApoptosisCarotid Artery InjuriesCell ProliferationCyclic GMPDisease Models, AnimalEnzyme ActivatorsGuanylate CyclaseIndazolesMalePhosphodiesterase InhibitorsPurinonesRatsRats, Sprague-Dawley3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazoleCyclic GMPEnzyme ActivatorsGuanylate CyclaseIndazolesPhosphodiesterase InhibitorsPurinoneszaprinast

Identifiers

PMID19342499
PMCPMC2702762
OpenAlexW2158519096

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.