Evidence map›Paper›PMID 21441141›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2011

Peroxisome proliferator-activated receptor-α activation promotes macrophage reverse cholesterol transport through a liver X receptor-dependent pathway.

Kazuhiro Nakaya, Junichiro Tohyama, Snehal U Naik, Hiroyuki Tanigawa, Colin MacPhee, Jeffrey T Billheimer, Daniel J Rader

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Adelmidrol protects against non-alcoholic steatohepatitis in mice.Naunyn-Schmiedeberg's archives of pharmacology · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Liver X receptors, atherosclerosis and inflammation.Current atherosclerosis reports · 2012
    Review
  16. 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

7 authors at 1 institution in 1 country.

Kazuhiro NakayaDepartment of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Junichiro Tohyama
Snehal U Naik
Hiroyuki Tanigawa
Colin MacPhee
Jeffrey T Billheimer
Daniel J Rader
GlaxoSmithKline (United Kingdom) · GB

Funding

Oxidative Modifications of Proteins and Fibrinogen in AtherosclerosisP50HL070128 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2002 to 2006
$10.8M
NHLBI NIH HHS P50 HL070128NHLBI NIH HHS P50-HL70128
6 · The paper itself

Abstract

objectivePeroxisome proliferator-activated receptor-α (PPARα) activation has been shown in vitro to increase macrophage cholesterol efflux, the initial step in reverse cholesterol transport (RCT). However, it remains unclear whether PPARα activation promotes macrophage RCT in vivo. METHODS AND

resultsWe demonstrated that a specific potent PPARα agonist GW7647 inhibited atherosclerosis and promoted macrophage RCT in hypercholesterolemic mice expressing the human apolipoprotein A-I (apoA-I) gene. We compared the effect of GW7647 on RCT in human apoA-I transgenic (hA-ITg) mice with wild-type mice and showed that the PPARα agonist promoted RCT in hA-ITg mice to a much greater extent than in wild-type mice, indicating that human apoA-I expression is important for PPARα-induced RCT. We further investigated the dependence of the macrophage PPARα-liver X receptor (LXR) pathway on the promotion of RCT by GW7647. Primary murine macrophages lacking PPARα or LXR abolished the ability of GW7647 to promote RCT in hA-ITg mice. In concert, the PPARα agonist promoted cholesterol efflux and ATP binding cassette transporter A1/G1 expression in primary macrophages, and this was also by the PPARα-LXR pathway.

conclusionOur observations demonstrate that a potent PPARα agonist promotes macrophage RCT in vivo in a manner that is enhanced by human apoA-I expression and dependent on both macrophage PPARα and LXR expression.

Indexed as

Signal TransductionAnimalsApolipoprotein A-IAtherosclerosisBiological TransportButyratesCholesterolHumansLiver X ReceptorsMacrophagesMiceOrphan Nuclear ReceptorsPhenylurea CompoundsPPAR alphaApolipoprotein A-IButyratesCholesterolGW 7647Liver X ReceptorsOrphan Nuclear ReceptorsPhenylurea CompoundsPPAR alpha

Identifiers

PMID21441141
PMCPMC3202300
OpenAlexW1989036024

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.