Evidence map›Paper›PMID 23360481›Full record

ArticleThe European journal of neuroscience2013

Estrogen-related receptor β deletion modulates whole-body energy balance via estrogen-related receptor γ and attenuates neuropeptide Y gene expression.

Mardi S Byerly, Muhannad Al Salayta, Roy D Swanson, Kiwook Kwon, Jonathan M Peterson, Zhikui Wei, Susan Aja, Timothy H Moran, Seth Blackshaw, G William Wong

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Genes & development · 2020
    Article
  8. Review
  9. Estrogen-related receptor β activation and isoform shifting by cdc2-like kinase inhibition restricts migration and intracranial tumor growth in glioblastoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  10. Article
  11. Review
  12. Brain nuclear receptors and body weight regulation.The Journal of clinical investigation · 2017
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Dynamic and extensive metabolic state-dependent regulation of cytokine expression and circulating levels.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    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

10 authors at 2 institutions in 1 country.

Mardi S ByerlyDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. mardibyerly@gmail.com
Muhannad Al Salayta
Roy D Swanson
Kiwook Kwon
Jonathan M Peterson
Zhikui Wei
Susan Aja
Timothy H Moran
Seth Blackshaw
G William Wong
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI BRANCATI, FREDERICK L · 2013 to 2017
$9.7M
Diabetes Research and Training CenterP60DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI WONDISFORD, FREDRIC E. · 2008 to 2012
$9.1M
CTRP and Metabolic ControlR01DK084171 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Guang William Wong · 2010 to 2026
$8.0M
Interdepartmental Training Program in Cellular and Molecular EndocrinologyT32DK007751 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI WOLFE, ANDREW M · 1997 to 2016
$4.6M
The role of PIAS3 in retinal developmentR01EY017015 · NEI · JOHNS HOPKINS UNIVERSITY · PI BLACKSHAW, SETH · 2007 to 2017
$4.2M
Metabolic Characterization of the Novel Adipokine CTRP3F32DK084607 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI PETERSON, JONATHAN M · 2009 to 2011
$117k
NEI NIH HHS R01 EY017015NIDDK NIH HHS DK084171NIDDK NIH HHS F32 DK084607NIDDK NIH HHS F32DK084607NIDDK NIH HHS P30 DK079637NIDDK NIH HHS P60 DK079637NIDDK NIH HHS P60DK079637NIDDK NIH HHS R01 DK084171NIDDK NIH HHS T32 DK007751NIDDK NIH HHS T32DK007751
6 · The paper itself

Abstract

Estrogen-related receptors (ERRs) α, β and γ are orphan nuclear hormone receptors with no known ligands. Little is known concerning the role of ERRβ in energy homeostasis, as complete ERRβ-null mice die mid-gestation. We generated two viable conditional ERRβ-null mouse models to address its metabolic function. Whole-body deletion of ERRβ in Sox2-Cre:ERRβ(lox/lox) mice resulted in major alterations in body composition, metabolic rate, meal patterns and voluntary physical activity levels. Nestin-Cre:ERRβ(lox/lox) mice exhibited decreased expression of ERRβ in hindbrain neurons, the predominant site of expression, decreased neuropeptide Y (NPY) gene expression in the hindbrain, increased lean body mass, insulin sensitivity, increased energy expenditure, decreased satiety and decreased time between meals. In the absence of ERRβ, increased ERRγ signaling decreased satiety and the duration of time between meals, similar to meal patterns observed for both the Sox2-Cre:ERRβ(lox/lox) and Nestin-Cre:ERRβ(lox/lox) strains of mice. Central and/or peripheral ERRγ signaling may modulate these phenotypes by decreasing NPY gene expression. Overall, the relative expression ratio between ERRβ and ERRγ may be important in modulating ingestive behavior, specifically satiety, gene expression, as well as whole-body energy balance.

Indexed as

Energy MetabolismAnimalsBody WeightGene DeletionGene ExpressionInsulin ResistanceMiceMice, KnockoutNeuronsNeuropeptide YPhenotypeReceptors, EstrogenRhombencephalonSatiationSignal TransductionEsrrb protein, mouseEsrrg protein, mouseNeuropeptide YReceptors, Estrogen

Identifiers

PMID23360481
PMCPMC3618562
OpenAlexW1989650788

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.