Evidence map›Paper›PMID 17950663›Full record

ArticleBiochimica et biophysica acta2007

Inability to fully suppress sterol synthesis rates with exogenous sterol in embryonic and extraembyronic fetal tissues.

Lihang Yao, Katie Jenkins, Paul S Horn, M Hayden Lichtenberg, Laura A Woollett

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Multiparity leads to obesity and inflammation in mothers and obesity in male offspring.American journal of physiology. Endocrinology and metabolism · 2012
    Article
  6. Article
  7. Article
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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

5 authors at 1 institution in 1 country.

Lihang YaoDepartment of Pathology and Laboratory Medicine, 2180 E. Galbraith Rd, Genome Research Institute, University of Cincinnati Medical Center, Cincinnati, OH 45237-0507, USA.
Katie Jenkins
Paul S Horn
M Hayden Lichtenberg
Laura A Woollett
University of Cincinnati · US

Funding

STEROL METABOLISM DURING PREGNANCY AND DEVELOPMENTR01HD034089 · NICHD · UNIVERSITY OF CINCINNATI · PI WOOLLETT, LAURA A · 1997 to 2005
$1.4M
Sterol Metabolism During Pregnancy and DevelopmentR56HD034089 · NICHD · UNIVERSITY OF CINCINNATI · PI WOOLLETT, LAURA A · 2008 to 2008
$298k
NICHD NIH HHS HD34089NICHD NIH HHS R01 HD034089NICHD NIH HHS R56 HD034089
6 · The paper itself

Abstract

The requirement for cholesterol is greater in developing tissues (fetus, placenta, and yolk sac) as compared to adult tissues. Here, we compared cholesterol-induced suppression of sterol synthesis rates in the adult liver to the fetal liver, fetal body, placenta, and yolk sac of the Golden Syrian hamster. Sterol synthesis rates were suppressed maximally in non-pregnant adult livers when cholesterol concentrations were increased. In contrast, sterol synthesis rates were suppressed only marginally in fetal livers, fetal bodies, placentas, and yolk sacs when cholesterol concentrations were increased. To begin to elucidate the mechanism responsible for the blunted response of sterol synthesis rates in fetal tissues to exogenous cholesterol, the ratio of sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCAP) to Insig-1 was measured in these same tissues since the ratio of SCAP to the Insigs can impact SREBP processing. The fetal tissues had anywhere from a 2- to 6-fold greater ratio of SCAP to Insig-1 than did the adult liver, suggesting constitutive processing of the SREBPs. As expected, the level of mature, nuclear SREBP-2 was not different in the fetal tissues with different levels of cholesterol whereas it was different in adult livers. These findings indicate that the suppression of sterol synthesis to exogenous sterol is blunted in developing tissues and the lack of response appears to be mediated at least partly through relative levels of Insigs and SCAP.

Indexed as

AnimalsBase SequenceCholesterolCricetinaeCyclophilinsDNA PrimersFemaleFetusIntracellular Signaling Peptides and ProteinsKineticsLiverMaleMembrane ProteinsMesocricetusPlacentaPregnancyCholesterolCyclophilinsDNA PrimersIntracellular Signaling Peptides and ProteinsMembrane ProteinsRNA, MessengerSREBP cleavage-activating proteinSterols

Identifiers

PMID17950663
PMCPMC2711845
OpenAlexW2033119686

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.