Evidence map›Paper›PMID 23748190›Full record

ArticleInternational journal of obesity (2005)2014

Fetal baboon sex-specific outcomes in adipocyte differentiation at 0.9 gestation in response to moderate maternal nutrient reduction.

Y D Tchoukalova, R Krishnapuram, U A White, D Burk, X Fang, M J Nijland, P W Nathanielsz

Open access · bronzeAbstract read
In one paragraph

Article in International journal of obesity (2005), 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
0.4field-weighted citation impact, top 36% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Thermoneutrality effects on developmental programming of obesity.Journal of developmental origins of health and disease · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Why primate models matter.American journal of primatology · 2014
    Review
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 4 institutions in 1 country.

Y D TchoukalovaDepartment of Biology of Adipose Tissue Depots, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.
R KrishnapuramDepartment of Biology of Adipose Tissue Depots, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.
U A WhiteDepartment of Biology of Adipose Tissue Depots, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.
D BurkDepartment of Biology of Adipose Tissue Depots, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.
X FangDivision of Health Economics, Louisiana State Department of Health and Hospitals, Baton Rouge, LA, USA.
M J NijlandCenter for Pregnancy and Newborn Research, University of Texas Health Science Center, San Antonio, TX, USA.
P W NathanielszCenter for Pregnancy and Newborn Research, University of Texas Health Science Center, San Antonio, TX, USA.
Louisiana State University System · USThe University of Texas Health Science Center at San Antonio · USLouisiana State Department of Health and Hospitals · USPennington Biomedical Research Center · US

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
PARTURITION AND FETAL PRIMATE HYPOTHALAMIC FUNCTIONP01HD021350 · NICHD · UNIVERSITY OF WYOMING · PI NIJLAND, MARK J · 1987 to 2018
$19.9M
THE ROLE OF PROTEIN MALNUTRITION ON CIRCADIAN PHYSIOLOGY OF C57BL/6J MOUSE DAMSP20RR021945 · NCRR · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2006 to 2011
$9.5M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Poor nutrition and fetal development: preadipocyte adaptation in a primate modelR03HD060158 · NICHD · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI TCHOUKALOVA, YOURKA DIMOVA · 2009 to 2010
$148k
NCRR NIH HHS P20 RR021945NCRR NIH HHS P20-RR021945NICHD NIH HHS HD21350NICHD NIH HHS P01 HD021350NICHD NIH HHS R03 HD060158NICHD NIH HHS R03-HD 060158NIDDK NIH HHS 1P30-DK072476NIDDK NIH HHS P30 DK072476NIGMS NIH HHS P20 GM103528NIGMS NIH HHS P30 GM118430NIH HHS P51 OD011133
6 · The paper itself

Abstract

objectiveTo investigate in vitro adipocyte differentiation in baboon fetuses in response to reduced maternal nutrition.

designCross-sectional comparison of adipocyte differentiation in normally grown fetuses and fetuses of pregnant baboons fed 70% of the control global diet from 30 days of pregnancy to term. SUBJECTS: The subjects comprised control (CTR) fetuses (five female and five male) of mothers fed ad libitum and fetuses of mothers fed 70% of the global diet consumed by CTR (maternal nutrient reduction (MNR), five female and five male fetuses). The expression of genes/proteins involved in adipogenesis (PPARγ, FABP4 and adiponectin) and brown adipose tissue development (UCP1, TBX15 and COXIV) were determined in in vitro-differentiated stromal-vascular cultures from subcutaneous abdominal, subcutaneous femoral and omental adipose tissue depots. Adipocyte number per area (mm(2)) was determined histologically to assist in the evaluation of adipocyte size.

resultsMaternal suboptimal nutrition suppressed growth of male but not female fetuses and led to adipocyte hypertrophy accompanied by increased markers of white- and, particularly, brown-type adipogenesis in male but not female fetuses.

conclusionAdipose tissue responses to fetal nonhuman primate undernutrition are sexually dimorphic. While female fetuses adapt adequately, the male ones enhance pathways involved in white and brown adipose tissue development but are unable to compensate for a delayed development of adipose tissue associated with intrauterine growth restriction. These differences need to be considered when assessing developmental programming of adiposity in response to suboptimal maternal nutrition.

Indexed as

Animal Nutritional Physiological PhenomenaMaternal Nutritional Physiological PhenomenaPrenatal Nutritional Physiological PhenomenaAdipocytesAdipogenesisAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCell DifferentiationFatty Acid-Binding ProteinsFemaleFetal DevelopmentFetusGene Expression Regulation, DevelopmentalGestational AgeHumansFABP4 protein, humanFatty Acid-Binding ProteinsPPAR alpha

Identifiers

PMID23748190
PMCPMC3883997
OpenAlexW2015603017

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.