Evidence map›Paper›PMID 24670668›Full record

ArticlePloS one2014

Expression of adrenoceptor subtypes in preterm piglet heart is different to term heart.

Min Young Kim, Angela M Finch, Eugenie R Lumbers, Amanda C Boyce, Karen J Gibson, Yvonne A Eiby, Barbara E Lingwood

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
2.2field-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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Dexmedetomidine's effect on neonatal sedation, pain, respiratory status and cardiovascular system.Journal of perinatology : official journal of the California Perinatal Association · 2025
    Article
  6. Ductus Arteriosus in Fetal and Perinatal Life.Journal of cardiovascular development and disease · 2024
    Review
  7. Review
  8. Review
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  11. Article
  12. Article
  13. Review
  14. Article
  15. Is the ferret a suitable species for studying perinatal brain injury?International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2015
    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 3 institutions in 1 country.

Min Young KimThe University of Queensland, UQ Centre for Clinical Research, Brisbane, Australia.
Angela M FinchDepartment of Pharmacology, School of Medical Sciences, The University of New South Wales, Sydney, Australia.
Eugenie R LumbersThe University of Queensland, UQ Centre for Clinical Research, Brisbane, Australia; Department of Physiology, School of Medical Sciences, The University of New South Wales, Sydney, Australia; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, Australia.
Amanda C BoyceDepartment of Physiology, School of Medical Sciences, The University of New South Wales, Sydney, Australia.
Karen J GibsonDepartment of Physiology, School of Medical Sciences, The University of New South Wales, Sydney, Australia.
Yvonne A EibyThe University of Queensland, UQ Centre for Clinical Research, Brisbane, Australia.
Barbara E LingwoodThe University of Queensland, UQ Centre for Clinical Research, Brisbane, Australia.
University of Queensland · AUUNSW Sydney · AUUniversity of Newcastle Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preterm delivery increases the risk of inadequate systemic blood flow and hypotension, and many preterm infants fail to respond to conventional inotrope treatments. If the profile of cardiac adrenoceptor subtypes in the preterm neonate is different to that at term this may contribute to these clinical problems. This study measured mRNA expression of β1, β2, α1A, α2A and α2B-adrenoceptor subtypes by real time PCR in term (113d), preterm (91d) and preterm piglets (91d) exposed to maternal glucocorticoid treatment. Abundance of β-adrenoceptor binding sites in the left ventricle was measured using saturation binding assays. Relative abundance of β1-adrenoceptor mRNA in untreated preterm hearts was ∼50% of term abundance in both left and right ventricles (P<0.001). Trends in receptor binding site density measurements supported this observation (P = 0.07). Glucocorticoid exposure increased β1-adrenoceptor mRNA levels in the right ventricle of preterm hearts (P = 0.008) but did not alter expression in the left ventricle (P>0.1). Relative abundance of α1A-adrenoceptor mRNA was the same in preterm and term piglet hearts (P = >0.1) but was reduced by maternal glucocorticoid treatment (P<0.01); α2A-adrenoceptor mRNA abundance was higher in untreated and glucocorticoid exposed preterm piglet hearts than in term piglets (P<0.001). There was no difference between male and female piglets in mRNA abundance of any of the genes studied. In conclusion, there is reduced mRNA abundance of β1-adrenoceptors in the preterm pig heart. If this lower expression of β-adrenoceptors occurs in human preterm infants, it could explain their poor cardiovascular function and their frequent failure to respond to commonly used inotropes.

Indexed as

AnimalsBinding SitesFemaleGene Expression Regulation, DevelopmentalHeartMaleMyocardiumPremature BirthReceptors, AdrenergicReceptors, Adrenergic, alphaReceptors, Adrenergic, betaSus scrofaTerm BirthReceptors, AdrenergicReceptors, Adrenergic, alphaReceptors, Adrenergic, beta

Identifiers

PMID24670668
PMCPMC3966759
OpenAlexW2030268254

What OpenQuestion holds

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LicenceCC BY
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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.