Evidence map›Paper›PMID 31110021›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

NURR1 activation in skeletal muscle controls systemic energy homeostasis.

Leonela Amoasii, Efrain Sanchez-Ortiz, Teppei Fujikawa, Joel K Elmquist, Rhonda Bassel-Duby, Eric N Olson

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

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  11. Enhancement of physiology via adaptive transcription.Pflugers Archiv : European journal of physiology · 2025
    Review
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  13. Science advances · 2024
    Article
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  18. NURR1 expression regulates retinal pigment epithelial-mesenchymal transition and age-related macular degeneration phenotypes.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  19. Review
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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.

Leonela AmoasiiDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Efrain Sanchez-OrtizDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Teppei FujikawaDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Joel K ElmquistDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Rhonda Bassel-DubyDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Eric N OlsonDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390; eric.olson@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

Deciphering the role of a novel micropeptide in cardiac function and dysfunctionR01HL130253 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI BASSEL-DUBY, RHONDA, OLSON, ERIC N · 2016 to 2023
$4.4M
Metabolic Control by Myogenic MicroRNAs, Mediator and MyokinesR01DK099653 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BASSEL-DUBY, RHONDA, OLSON, ERIC N · 2013 to 2016
$1.9M
Molecular Dissection of Myoblast Fusion In Muscle Development and RegenerationR01AR067294 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI BASSEL-DUBY, RHONDA, OLSON, ERIC N · 2015 to 2019
$1.8M
Chemically assisted remodeling of infarcted heart tissue by targeting Wnt lipidationR01HL138426 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI BASSEL-DUBY, RHONDA · 2017 to 2020
$1.7M
NHLBI NIH HHS R01 HL130253NHLBI NIH HHS R01 HL138426NIAMS NIH HHS R01 AR067294NIDDK NIH HHS R01 DK099653
6 · The paper itself

Abstract

Skeletal muscle plays a central role in the control of metabolism and exercise tolerance. Analysis of muscle enhancers activated after exercise in mice revealed the orphan nuclear receptor NURR1/NR4A2 as a prominent component of exercise-responsive enhancers. We show that exercise enhances the expression of NURR1, and transgenic overexpression of NURR1 in skeletal muscle enhances physical performance in mice. NURR1 expression in skeletal muscle is also sufficient to prevent hyperglycemia and hepatic steatosis, by enhancing muscle glucose uptake and storage as glycogen. Furthermore, treatment of obese mice with putative NURR1 agonists increases energy expenditure, improves glucose tolerance, and confers a lean phenotype, mimicking the effects of exercise. These findings identify a key role for NURR1 in governance of skeletal muscle glucose metabolism, and reveal a transcriptional link between exercise and metabolism. Our findings also identify NURR1 agonists as possible exercise mimetics with the potential to ameliorate obesity and other metabolic abnormalities.

Indexed as

AnimalsCarbohydrate MetabolismEnergy MetabolismFatty LiverGlucoseGlycogenHomeostasisHumansHyperglycemiaLiverMaleMiceMice, Inbred C57BLMuscle, SkeletalNuclear Receptor Subfamily 4, Group A, Member 2ObesityGlucoseGlycogenNr4a2 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 2exerciseMediator complexmetabolic syndromenuclear receptorobesity

Identifiers

PMID31110021
PMCPMC6561277
OpenAlexW2945171190

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.