Evidence map›Paper›PMID 23238296›Full record

ArticleDiabetes2013

Adipose deficiency of Nrf2 in ob/ob mice results in severe metabolic syndrome.

Peng Xue, Yongyong Hou, Yanyan Chen, Bei Yang, Jingqi Fu, Hongzhi Zheng, Kathy Yarborough, Courtney G Woods, Dianxin Liu, Masayuki Yamamoto and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

82 citing papers in PubMed, 162 citations in OpenAlex.

  1. Trial
  2. Hepatocyte-SpecificAntioxidants (Basel, Switzerland) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Adipose tissue-specificFrontiers in endocrinology · 2025
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Protective Effects of Curcumin and its AnaloguesCurrent medicinal chemistry · 2024
    Review
  20. Article

22 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 3 countries.

Peng XueInstitute for Chemical Safety Sciences, The Hamner Institutes for Health Sciences, Research Triangle Park, North Carolina, USA.
Yongyong Hou
Yanyan Chen
Bei Yang
Jingqi Fu
Hongzhi Zheng
Kathy Yarborough
Courtney G Woods
Dianxin Liu
Masayuki Yamamoto
Qiang Zhang
Melvin E Andersen
Jingbo Pi
Research Triangle Park Foundation · USSanford Burnham Prebys Medical Discovery Institute · USThe Hamner Institutes for Health Sciences · USTohoku University · JP

Funding

Paradoxical roles of Nrf2 activation in arsenic-induced beta-cell dysfunctionR01ES016005 · NIEHS · THE HAMNER INSTITUTES · PI PI, JINGBO · 2008 to 2012
$2.5M
Paradoxical Roles of Reactive Oxygen Species in Pancreatic Beta-Cell FunctionK01DK076788 · NIDDK · THE HAMNER INSTITUTES · PI PI, JINGBO · 2007 to 2009
$358k
NIDDK NIH HHS DK-76788NIDDK NIH HHS K01 DK076788NIEHS NIH HHS ES016005NIEHS NIH HHS R01 ES016005
6 · The paper itself

Abstract

Nuclear factor E2-related factor 2 (Nrf2) is a transcription factor that functions as a master regulator of the cellular adaptive response to oxidative stress. Our previous studies showed that Nrf2 plays a critical role in adipogenesis by regulating expression of CCAAT/enhancer-binding protein β and peroxisome proliferator-activated receptor γ. To determine the role of Nrf2 in the development of obesity and associated metabolic disorders, the incidence of metabolic syndrome was assessed in whole-body or adipocyte-specific Nrf2-knockout mice on a leptin-deficient ob/ob background, a model with an extremely positive energy balance. On the ob/ob background, ablation of Nrf2, globally or specifically in adipocytes, led to reduced white adipose tissue (WAT) mass, but resulted in an even more severe metabolic syndrome with aggravated insulin resistance, hyperglycemia, and hypertriglyceridemia. Compared with wild-type mice, WAT of ob/ob mice expressed substantially higher levels of many genes related to antioxidant response, inflammation, adipogenesis, lipogenesis, glucose uptake, and lipid transport. Absence of Nrf2 in WAT resulted in reduced expression of most of these factors at mRNA or protein levels. Our findings support a novel role for Nrf2 in regulating adipose development and function, by which Nrf2 controls the capacity of WAT expansion and insulin sensitivity and maintains glucose and lipid homeostasis.

Indexed as

AdiposityGene Expression RegulationAdipogenesisAdipose Tissue, WhiteAnimalsCrosses, GeneticFemaleGene Expression ProfilingHyperglycemiaHypertriglyceridemiaInsulin ResistanceMaleMetabolic SyndromeMiceMice, KnockoutMice, ObeseNfe2l2 protein, mouseNF-E2-Related Factor 2RNA, Messenger

Identifiers

PMID23238296
PMCPMC3581189
OpenAlexW2110982489

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.