Evidence map›Paper›PMID 23576437›Full record

ArticleThe Journal of biological chemistry2013

Soluble epoxide hydrolase deficiency or inhibition attenuates diet-induced endoplasmic reticulum stress in liver and adipose tissue.

Ahmed Bettaieb, Naoto Nagata, Daniel AbouBechara, Samah Chahed, Christophe Morisseau, Bruce D Hammock, Fawaz G Haj

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
5.1field-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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  9. ACS medicinal chemistry letters · 2024
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  12. Review
  13. Differential lipid signaling from CD4Frontiers in immunology · 2024
    Article
  14. Article
  15. Soluble epoxide hydrolase-targeting PROTAC activates AMPK and inhibits endoplasmic reticulum stress.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    Article
  16. Article
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20 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

7 authors at 1 institution in 1 country.

Ahmed BettaiebDepartment of Nutrition, University of California, Davis, California 95616.
Naoto NagataDepartment of Nutrition, University of California, Davis, California 95616.
Daniel AbouBecharaDepartment of Nutrition, University of California, Davis, California 95616.
Samah ChahedDepartment of Nutrition, University of California, Davis, California 95616.
Christophe MorisseauDepartment of Entomology, University of California, Davis, California 95616; Comprehensive Cancer Center, University of California, Davis, California 95616.
Bruce D HammockDepartment of Entomology, University of California, Davis, California 95616; Comprehensive Cancer Center, University of California, Davis, California 95616.
Fawaz G HajDepartment of Nutrition, University of California, Davis, California 95616; Comprehensive Cancer Center, University of California, Davis, California 95616; Department of Internal Medicine, University of California, Davis, California 95616. Electronic address: fghaj@ucdavis.edu.
University of California, Davis · US

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI YOUNG, THOMAS MICHAEL · 1987 to 2021
$50.1M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR01ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1985 to 2018
$4.0M
OXYGENASE METABOLITES AND RENAL VASCULAR ACTIVITYR01HL059699 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI IMIG, JOHN D · 1999 to 2011
$3.0M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR37ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1998 to 2007
$3.0M
Role of adipose protein-tyrosine phosphatase 1B in glucose homeostasis and body mR01DK090492 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAJ, FAWAZ GEORGE · 2011 to 2015
$1.7M
Role of Protein-Tyrosine Phosphatase 1B in Pancreatic Islet FunctionR56DK084317 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAJ, FAWAZ GEORGE · 2010 to 2010
$230k
OXYGENASE METABOLITES AND RENAL VASCULAR ACTIVITYR29HL059699 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI IMIG, JOHN D · 1998 to 1998
–
NHLBI NIH HHS HL059699NHLBI NIH HHS R01 HL059699NIDDK NIH HHS R01 DK090492NIDDK NIH HHS R56 DK084317NIEHS NIH HHS ES02710NIEHS NIH HHS P42 ES004699NIEHS NIH HHS P42 ES04699NIEHS NIH HHS R01 ES002710NIEHS NIH HHS R37 ES002710
6 · The paper itself

Abstract

Soluble epoxide hydrolase (sEH) is a cytosolic enzyme whose inhibition has beneficial effects in cardiovascular, inflammatory, and metabolic diseases in murine models. Mice with targeted deletion or pharmacological inhibition of sEH exhibit improved insulin signaling in liver and adipose tissue. Herein, we assessed the role of sEH in regulating endoplasmic reticulum (ER) stress in liver and adipose tissue. We report that sEH expression was increased in the livers and adipose tissue of mice fed a high fat diet, the adipose tissue of overweight humans, and palmitate-treated cells. Importantly, sEH deficiency or inhibition in mice attenuated chronic high fat diet-induced ER stress in liver and adipose tissue. Similarly, pharmacological inhibition of sEH in HepG2 cells and 3T3-L1 adipocytes mitigated chemical-induced ER stress and activation of JNK, p38, and cell death. In addition, insulin signaling was enhanced in HepG2 cells treated with sEH substrates and attenuated in cells treated with sEH products. In summary, these findings demonstrate that sEH is a physiological modulator of ER stress and a potential target for mitigating complications associated with obesity.

Indexed as

DietEndoplasmic Reticulum StressGene Expression Regulation3T3-L1 CellsAdipose TissueAnimalsCytosolEpoxide HydrolasesFatty Acids, UnsaturatedHep G2 CellsHumansHydrolasesInflammationInsulinInsulin ResistanceLiverEPHX2 protein, humanEphx2 protein, mouseEpoxide HydrolasesFatty Acids, UnsaturatedHydrolasesInsulinEndoplasmic Reticulum StressEpoxyeicosatrienoic Acids (EETs)HydrolasesInflammationInsulin ResistanceMetabolic RegulationSoluble Epoxide Hydrolase

Identifiers

PMID23576437
PMCPMC3656275
OpenAlexW2140116636

What Socratic 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 Socratic graph.