Evidence map›Paper›PMID 21173252›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Both liver-X receptor (LXR) isoforms control energy expenditure by regulating brown adipose tissue activity.

Marion Korach-André, Amena Archer, Rodrigo P Barros, Paolo Parini, Jan-Åke Gustafsson

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
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  10. Small molecules for fat combustion: targeting obesity.Acta pharmaceutica Sinica. B · 2019
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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

5 authors at 3 institutions in 2 countries.

Marion Korach-AndréDepartment of Biosciences and Nutrition at NOVUM, Karolinska Institutet, 14183 Huddinge, Sweden. marion.korach-andre@ki.se
Amena Archer
Rodrigo P Barros
Paolo Parini
Jan-Åke Gustafsson
Karolinska Institutet · SEKarolinska University Hospital · SEUniversity of Houston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brown adipocytes are multilocular lipid storage cells that play a crucial role in nonshivering thermogenesis. Uncoupling protein 1 (UCP1) is a unique feature of brown fat cells that allows heat generation on sympathetic nervous system stimulation. As conventional transcriptional factors that are activated in various signaling pathways, liver-X receptors (LXRs) play important roles in many physiological processes. The role of LXRs in the regulation of energy homeostasis remains unclear, however. Female WT, LXRαβ(-/-), LXRα(-/-), and LXRβ(-/-) mice were fed with either a normal diet (ND) or a high-carbohydrate diet (HCD) supplemented with or without GW3965-LXR agonist. LXRαβ(-/-) mice exhibited higher energy expenditure (EE) as well as higher UCP1 expression in brown adipose tissue (BAT) compared with WT mice on the HCD. In addition, long-term treatment of WT mice with GW3965 showed lower EE at thermoneutrality (30 °C) and lower Ucp1 expression level in BAT. Furthermore, H&E staining of the BAT of LXRαβ(-/-) mice exhibited decreased lipid droplet size compared with WT mice on the HCD associated with a more intense UCP1-positive reaction. Quantification of triglyceride (TG) content in BAT showed lower TG accumulation in LXRβ(-/-) mice compared with WT mice. Surprisingly, GW3965 treatment increased TG content (twofold) in the BAT of WT and LXRα(-/-) mice but not in LXRβ(-/-) mice. Furthermore, glucose transporter (GLUT4) in the BAT of LXRα(-/-) and LXRβ(-/-) mice was sixfold and fourfold increased, respectively, compared with WT mice on the ND. These findings suggest that LXRα as well as LXRβ could play a crucial role in the regulation of energy homeostasis in female mice and may be a potential target for the treatment of obesity and energy regulation.

Indexed as

Adipose Tissue, BrownAnalysis of VarianceAnimalsBenzoatesBenzylaminesBlood GlucoseBlotting, WesternCalorimetryEnergy MetabolismFemaleGlucose Transporter Type 4ImmunohistochemistryIon ChannelsLiver X ReceptorsMagnetic Resonance ImagingMiceBenzoatesBenzylaminesBlood GlucoseGlucose Transporter Type 4GW 3965Ion ChannelsLiver X ReceptorsMitochondrial ProteinsNr1h3 protein, mouseOrphan Nuclear ReceptorsProtein IsoformsSlc2a4 protein, mouseTriglyceridesUcp1 protein, mouseUncoupling Protein 1

Identifiers

PMID21173252
PMCPMC3017156
OpenAlexW2154539035

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.