Evidence map›Paper›PMID 38035825›Full record

ArticleEndocrinology2023

Elevated Norepinephrine Stimulates Adipocyte Hyperplasia in Ovine Fetuses With Placental Insufficiency and IUGR.

Rosa I Luna-Ramirez, Amy C Kelly, Miranda J Anderson, Christopher A Bidwell, Ravi Goyal, Sean W Limesand

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 1 country.

Rosa I Luna-RamirezSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ 85719, USA.
Amy C KellySchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ 85719, USA.ORCID 0000-0002-7792-1516
Miranda J AndersonSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ 85719, USA.
Christopher A BidwellDepartment of Animal Sciences, Purdue University, West Lafayette, IN 47906, USA.
Ravi GoyalSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ 85719, USA.ORCID 0000-0003-2940-0051
Sean W LimesandSchool of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ 85719, USA.ORCID 0000-0002-5851-0439
University of Arizona · USPurdue University West Lafayette · US

Funding

Prevention of Placental Insufficiency Improves Beta-Cells FunctionR01DK084842 · NIDDK · UNIVERSITY OF ARIZONA · PI SEAN W LIMESAND · 2009 to 2026
$5.6M
NIDDK NIH HHS R01 DK084842NIH HHS RO1 DK084842
6 · The paper itself

Abstract

Prevailing hypoxemia and hypoglycemia in near-term fetuses with placental insufficiency-induced intrauterine growth restriction (IUGR) chronically increases norepinephrine concentrations, which lower adrenergic sensitivity and lipid mobilization postnatally, indicating a predisposition for adiposity. To determine adrenergic-induced responses, we examined the perirenal adipose tissue transcriptome from IUGR fetuses with or without hypercatecholaminemia. IUGR was induced in sheep with maternal hyperthermia, and hypercatecholaminemia in IUGR was prevented with bilateral adrenal demedullation. Adipose tissue was collected from sham-operated control (CON) and IUGR fetuses and adrenal-demedullated control (CAD) and IUGR (IAD) fetuses. Norepinephrine concentrations were lower in IAD fetuses than in IUGR fetuses despite both being hypoxemic and hypoglycemic. In IUGR fetuses, perirenal adipose tissue mass relative to body mass was greater compared with the CON, adrenal-demedullated control, and IAD groups. Transcriptomic analysis identified 581 differentially expressed genes (DEGs) in CON vs IUGR adipose tissue and 193 DEGs in IUGR vs IAD adipose tissue. Integrated functional analysis of these 2 comparisons showed enrichment for proliferator-activated receptor signaling and metabolic pathways and identified adrenergic responsive genes. Within the adrenergic-regulated DEGs, we identified transcripts that regulate adipocyte proliferation and differentiation: adipogenesis regulatory factor, C/CCAAT/enhancer binding protein α, and sterol carrier protein 2. DEGs associated with the metabolic pathway included pyruvate dehydrogenase kinase 4, 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4, IGF-binding proteins (IGFBP-5 and IGFBP-7). Sex-specific expression differences were also found for adipogenesis regulatory factor, pyruvate dehydrogenase kinase 4, IGFBP5, and IGFBP7. These findings indicate that sustained adrenergic stimulation during IUGR leads to adipocyte hyperplasia with alterations in metabolism, proliferation, and preadipocyte differentiation pathways.

Indexed as

Fetal Growth RetardationPlacental InsufficiencyAdipocytesAdrenergic AgentsAnimalsFemaleFetusHumansHyperplasiaMaleNorepinephrinePlacentaPregnancySheepAdrenergic AgentsNorepinephrineadipogenesis regulatory factoradrenergic regulationcatecholaminesfetal growth restrictionPPAR signalingRNAseq

Identifiers

PMID38035825
PMCPMC10726312
OpenAlexW4389209766

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.