Evidence map›Paper›PMID 22268107›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2012

Expansion of the fetoplacental vasculature in late gestation is strain dependent in mice.

Monique Y Rennie, Jacqui Detmar, Kathie J Whiteley, Andrea Jurisicova, S Lee Adamson, John G Sled

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Allometric scaling relationships in mouse placenta.Journal of the Royal Society, Interface · 2022
    Article
  6. Placental metabolite profiles in late gestation for healthy mice.Metabolomics : Official journal of the Metabolomic Society · 2022
    Article
  7. Article
  8. Maternal background alters the penetrance of growth phenotypes and sex-specific placental adaptation of offspring sired by alcohol-exposed males.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  9. Article
  10. Placental vascular abnormalities in the mouse alter umbilical artery wave reflections.American journal of physiology. Heart and circulatory physiology · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Ultrasound detection of altered placental vascular morphology based on hemodynamic pulse wave reflection.American journal of physiology. Heart and circulatory physiology · 2017
    Article
  15. Placental Origins of Chronic Disease.Physiological reviews · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 2 countries.

Monique Y RennieMouse Imaging Centre, Toronto Centre for Phenogenomics, Hospital for Sick Children, Canada.
Jacqui Detmar
Kathie J Whiteley
Andrea Jurisicova
S Lee Adamson
John G Sled
Hospital for Sick Children · CALunenfeld-Tanenbaum Research Institute · CAMount Sinai Hospital · CA

Funding

Canadian Institutes of Health Research MOP86734Canadian Institutes of Health Research MOP93618
6 · The paper itself

Abstract

How the fetoplacental arterial tree grows and expands during late gestational development is largely unknown. In this study, we quantified changes in arterial branching in the fetal exchange region of the mouse placenta during late gestation, when capillarization increases rapidly. We studied two commonly used mouse strains, CD1 and C57Bl/6 (B6), at embryonic days (E)13.5, 15.5, and 17.5. B6 mice differ from CD1 mice by exhibiting a blunted fetal weight gain in late gestation. We found that B6 capillarization and interhemal membrane thinning were reduced and placental hypoxia-inducible factor-1α and VEGF-A expression were higher than CD1 near term. Automated vascular segmentation of microcomputed tomography data sets revealed that the number of arterial vessels ≥50 μm remained constant during late gestation in both strains, despite large increases in downstream capillary volume quantified by stereology (+65% in B6 mice and +200% in CD1 mice). Arterial diameters expanded in both strains from E13.5 to E15.5; however, diameters continued to expand to E17.5 in B6 mice only. The diameter scaling coefficient at branch sites was near optimal (-3.0) and remained constant in CD1 mice, whereas it decreased, becoming abnormal, in B6 mice at term (-3.5 ± 0.2). Based on arterial tree geometry, resistance remained constant throughout late gestation (∼0.45 mmHg·s·μl(-1)) in CD1 mice, whereas it decreased by 50% in late gestation in B6 mice. Quantification of the fetoplacental vasculature revealed significant strain-dependent differences in arterial and capillary expansion in late gestation. In both strains, enlargement of the fetoplacental arterial tree occurred primarily by increased arterial diameters with no change in segment numbers in late gestation.

Indexed as

Neovascularization, PhysiologicPlacental CirculationAnimalsArteriesBlotting, WesternCapillariesFemaleFetal WeightFetusGenotypeGestational AgeHemodynamicsHypoxia-Inducible Factor 1, alpha SubunitImmunohistochemistryLitter SizeMiceHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID22268107
PMCPMC3311476
OpenAlexW1988621470

What OpenQuestion holds

Textmetadata
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.