Evidence map›Paper›PMID 22423036›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2012

Regulation of cardiovascular development by adenosine and adenosine-mediated embryo protection.

Scott A Rivkees, Christopher C Wendler

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. A hypoxic episode during cardiogenesis downregulates the adenosinergic system and alters the myocardial anoxic tolerance.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  7. AHR2-Mediated transcriptomic responses underlying the synergistic cardiac developmental toxicity of PAHs.Toxicological sciences : an official journal of the Society of Toxicology · 2015
    Article
  8. Article
  9. Caffeine exposure alters cardiac gene expression in embryonic cardiomyocytes.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    Article
  10. Article
  11. 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

2 authors at 1 institution in 1 country.

Scott A RivkeesDepartment of Pediatrics, Yale Child Health Research Center, Yale University School of Medicine, New Haven CT, USA. scott.rivkees@yale.edu
Christopher C Wendler
Yale University · US

Funding

Adenosinergic Mechanisms of Intrauterine Growth RetardationR01HD058086 · NICHD · YALE UNIVERSITY · PI RIVKEES, SCOTT A. · 2009 to 2010
$824k
NICHD NIH HHS 1R01-HD056281NICHD NIH HHS R01 HD058086
6 · The paper itself

Abstract

Few signaling molecules have as much potential to influence the developing mammal as the nucleoside adenosine. Adenosine levels increase rapidly with tissue hypoxia and inflammation. Adenosine antagonists include the methylxanthines caffeine and theophylline. The receptors that transduce adenosine action are the A1, A2a, A2b, and A3 adenosine receptors (A1AR, A2aAR, A2bAR, and A3AR). We examined how adenosine acts via A1ARs to influence embryo development. Transgenic mice were studied along with embryo cultures. Embryos lacking A1ARs were markedly growth retarded following intrauterine hypoxia exposure. Studies of mice selectively lacking A1AR in the heart identify the heart as a key site of adenosine's embryo-protective effects. Studies of isolated embryos showed that adenosine plays a key role in modulating embryo cardiac function, especially in the setting of hypoxia. When pregnant mice were treated during embryogenesis with the adenosine antagonist caffeine, adult mice had abnormal heart function. Adenosine acts via A1ARs to play an essential role in protecting the embryo against intrauterine stress, and adenosine antagonists, including caffeine, may be an unwelcome exposure for the embryo.

Indexed as

Signal TransductionAbnormalities, Drug-InducedAdenosineAdenosine A1 Receptor AntagonistsAnimalsEmbryo Culture TechniquesHeartHeart Defects, CongenitalMiceMice, TransgenicMyocardiumReceptor, Adenosine A1AdenosineAdenosine A1 Receptor AntagonistsReceptor, Adenosine A1

Identifiers

PMID22423036
PMCPMC3306598
OpenAlexW1974998794

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.