Evidence map›Paper›PMID 30266429›Full record

ArticleBiochimica et biophysica acta. Molecular and cell biology of lipids2018

Maternal n-3 PUFA supplementation promotes fetal brown adipose tissue development through epigenetic modifications in C57BL/6 mice.

Rong Fan, Ashley Mulcahy Toney, Yura Jang, Seung-Hyun Ro, Soonkyu Chung

Abstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular and cell biology of lipids, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Brown Adipose Tissue and Its Role in Insulin and Glucose Homeostasis.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  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

5 authors at 1 institution in 1 country.

Rong FanDepartment of Nutrition and Health Sciences, University of Nebraska, Lincoln, NE 68583, USA.
Ashley Mulcahy ToneyDepartment of Nutrition and Health Sciences, University of Nebraska, Lincoln, NE 68583, USA.
Yura JangDepartment of Biochemistry, University of Nebraska, Lincoln, NE 68583, USA.
Seung-Hyun RoDepartment of Biochemistry, University of Nebraska, Lincoln, NE 68583, USA.
Soonkyu ChungDepartment of Nutrition and Health Sciences, University of Nebraska, Lincoln, NE 68583, USA. Electronic address: schung4@unl.edu.
University of Nebraska–Lincoln · US

Funding

The role of stress in the fetal origin of obesity and metabolic dysfunctionP20GM104320 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI ZEMPLENI, JANOS · 2014 to 2024
$24.9M
Epigenetic Regulation of fetal BAT Development via Maternal N-3 PUFA intakeR21HD094273 · NICHD · UNIVERSITY OF NEBRASKA LINCOLN · PI CHUNG, SOONKYU · 2019 to 2020
$416k
NICHD NIH HHS R21 HD094273NIGMS NIH HHS P20 GM104320
6 · The paper itself

Abstract

Brown adipose tissue (BAT) is a crucial regulator of energy expenditure. Emerging evidence suggests that n-3 PUFA potentiate brown adipogenesis in vitro. Since the pregnancy and lactation is a critical time for brown fat formation, we hypothesized that maternal supplementation of n-3 PUFA promotes BAT development in offspring. Female C57BL/6 mice were fed a diet containing n-3 PUFA (3%) derived from fish oil (FO), or an isocaloric diet devoid of n-3 PUFA (Cont) during pregnancy and lactation. Maternal n-3 PUFA intake was delivered to the BAT of neonates significantly reducing the n-6/n-3 ratio. The maternal n-3 PUFA exposure was linked with upregulated brown-specific gene and protein profiles and the functional cluster of brown-specific miRNAs. In addition, maternal n-3 PUFA induced histone modifications in the BAT evidenced by 1) increased epigenetic signature of brown adipogenesis, i.e., H3K27Ac and H3K9me2, 2) modified chromatin-remodeling enzymes, and 3) enriched the H3K27Ac in the promoter region of Ucp1. The offspring received maternal n-3 PUFA nutrition exhibited a significant increase in whole-body energy expenditure and better maintenance of core body temperature against acute cold treatment. Collectively, our results suggest that maternal n-3 PUFA supplementation potentiates fetal BAT development via the synergistic action of miRNA production and histone modifications, which may confer long-lasting metabolic benefits to offspring.

Indexed as

Adipose Tissue, BrownAnimalsChromatin Assembly and DisassemblyDietary SupplementsEnergy MetabolismEpigenesis, GeneticFatty Acids, Omega-3FemaleFish OilsGene Expression Regulation, DevelopmentalHistone CodeHistonesMiceMice, Inbred C57BLMicroRNAsPregnancyFatty Acids, Omega-3Fish OilsHistonesMicroRNAsUcp1 protein, mouseUncoupling Protein 1BATFish oilMaternal nutritionN-3 PUFAThermogenesis

Identifiers

PMID30266429
PMCPMC6203645
OpenAlexW2893582974

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.