Evidence map›Paper›PMID 25511504›Full record

ArticleJournal of cardiac surgery2015

Atorvastatin regulates apoptosis in chronically ischemic myocardium.

Ashraf A Sabe, Nassrene Y Elmadhun, Ahmed A Sadek, Rahul S Dalal, Louis M Chu, Cesario Bianchi, Frank W Sellke

Abstract read
In one paragraph

Article in Journal of cardiac surgery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 1 institution in 1 country.

Ashraf A SabeDivision of Cardiothoracic Surgery, Cardiovascular Research Center, Warren Alpert School of Medicine, Brown University, Providence, Rhode Island.
Nassrene Y Elmadhun
Ahmed A Sadek
Rahul S Dalal
Louis M Chu
Cesario Bianchi
Frank W Sellke
Brown University · US

Funding

Effect of Cardioplegia and Cardiopulmonary Bypass on Coronary Microvascular ReactivityR01HL046716 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W · 1997 to 2023
$8.5M
Surgical Intramyocardial Angiogenesis in a Swine Model of Endothelial DysfunctionR01HL069024 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W · 2002 to 2011
$3.7M
Brown CardioPulmonary Research Training ProgramT32HL094300 · NHLBI · RHODE ISLAND HOSPITAL · PI KOREN, GIDEON · 2008 to 2012
$2.2M
Angiogenesis in a model of diabetes and endothelial dysfunctionR01HL085647 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W · 2008 to 2009
$926k
Warren Alpert Medical School Basic Translational ResearchT35HL094308 · NHLBI · BROWN UNIVERSITY · PI Thomas Benedict Bartnikas, Brittany Star Hampton · 2009 to 2026
$808k
NHLBI NIH HHS 5T32-HL094300-03NHLBI NIH HHS R01 HL046716NHLBI NIH HHS R01 HL069024NHLBI NIH HHS R01 HL085647NHLBI NIH HHS R01HL46716NHLBI NIH HHS R01HL69024NHLBI NIH HHS T32 HL094300NHLBI NIH HHS T35 HL094308
6 · The paper itself

Abstract

backgroundWe previously demonstrated that atorvastatin upregulates proangiogenic proteins and increases arteriolar density in ischemic myocardium. Despite this, there was a lack of collateral-dependent perfusion, possibly related to apoptosis. We utilized a swine model of metabolic syndrome and chronic myocardial ischemia to investigate the effects of atorvastatin on apoptosis. MATERIALS AND

methodsSixteen Ossabaw miniswine were fed a high-cholesterol diet for 14 weeks then underwent surgical placement of an ameroid constrictor to their circumflex artery inducing chronic ischemia. Eight pigs additionally received supplemental atorvastatin (1.5 mg/kg daily). Myocardium was harvested six months later for western blotting and TUNEL staining.

resultsAnimals supplemented with atorvastatin had significant increases in markers associated with apoptosis including p-38, BAX, and caspase 3 (p < 0.05). Atorvastatin supplementation also resulted in significant increases in expression of cell survival proteins Bcl-2 and P-ERK and an overall decrease in apoptosis demonstrated by TUNEL staining (p < 0.05).

conclusionsAtorvastatin acts on multiple pathways and its effects on angiogenesis remain unclear. Although there is increased expression in several markers of apoptosis, key anti-apoptotic proteins were also upregulated with an overall decrease in apoptosis. Further investigation of these pathways may provide insight into the role of statins on myocardial protection after ischemia.

Indexed as

AnimalsApoptosisAtorvastatinbcl-2-Associated X ProteinCaspase 3Chronic DiseaseDisease Models, AnimalGene Expression Regulation, DevelopmentalHeptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsMAP Kinase Signaling SystemMetabolic SyndromeMyocardial IschemiaMyocardiumNeovascularization, PathologicPyrrolesAtorvastatinbcl-2-Associated X ProteinCaspase 3Heptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsPyrroles

Identifiers

PMID25511504
PMCPMC5645063
OpenAlexW1544823046

What OpenQuestion holds

Texttitle and abstract
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.