Evidence map›Paper›PMID 23584148›Full record

ReviewJournal of proteomics2013

Oxidative stress and protein carbonylation in adipose tissue - implications for insulin resistance and diabetes mellitus.

Tatjana Ruskovska, David A Bernlohr

Open access · greenAbstract readReview
In one paragraph

Review in Journal of proteomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Chchd10: A Novel Metabolic Sensor Modulating Adipose Tissue Homeostasis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. The Role of NADBiomedicines · 2023
    Review
  9. Article
  10. Redox Regulation of Lipid Mobilization in Adipose Tissues.Antioxidants (Basel, Switzerland) · 2021
    Review
  11. Article
  12. Article
  13. Antioxidative and Metabolic Effects ofNutrition and metabolic insights · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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

2 authors at 2 institutions in 2 countries.

Tatjana RuskovskaFaculty of Medical Sciences, Goce Delcev University, Stip, Former Yugolav Republic of Macedonia. Electronic address: tatjana.ruskovska@ugd.edu.mk.
David A Bernlohr
Goce Delcev University · MKUniversity of Minnesota · US

Funding

Obesity and Energy Metabolism CoreP30DK050456 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CROW, SCOTT J · 1995 to 2015
$17.0M
Mitochondrial Dysfunction and Adipose Insulin ResistanceR01DK084669 · NIDDK · UNIVERSITY OF MINNESOTA · PI BERNLOHR, DAVID A · 2010 to 2014
$1.6M
Mitochondrial Dysfunction and Adipose Insulin ResistanceR56DK084669 · NIDDK · UNIVERSITY OF MINNESOTA · PI BERNLOHR, DAVID A · 2009 to 2009
$185k
NIDDK NIH HHS DK050456NIDDK NIH HHS DK 084669NIDDK NIH HHS P30 DK050456NIDDK NIH HHS R01 DK084669NIDDK NIH HHS R56 DK084669
6 · The paper itself

Abstract

While historically considered simply as a depot for excess energy, white adipose tissue is a dynamically active endocrine organ capable of responding to a variety of efferent stimuli resulting in the synthesis and secretion of peptides, proteins and metabolites that serve as signal transducers to the peripheral and central circulation. Such regulation controls a variety of physiological processes including energy expenditure, food intake, reproductive capacity and responsiveness to insulin. Indeed, the accumulation of inflammatory cells in white adipose tissue is considered to be causative in the development of insulin resistance and eventually type 2 diabetes mellitus. A large body of evidence suggests that oxidative stress in adipose tissue not only correlates with insulin resistance but is also causative in its development. Moreover, using the available plasma oxidative stress biomarkers, many clinical studies have shown the presence of systemic oxidative stress in obese insulin resistant subjects, and its decrease after the successful treatment of obesity. In this review we emphasize the role of protein carbonylation in dysfunctional obese white adipose tissue and its metabolic implications. We focus on glutathione S-transferase A4 as the key enzyme for trans-4-hydroxy-2-nonenal and trans-4-oxo-2-nonenal removal from the cell, thus preventing protein carbonylation. This article is part of a Special Issue entitled: Posttranslational Protein modifications in biology and Medicine.

Indexed as

Insulin ResistanceOxidative StressProtein CarbonylationProtein Processing, Post-TranslationalAdipose TissueAnimalsBiomarkersDiabetes Mellitus, Type 2HumansObesityBiomarkersAdipose tissueGlutathione S-transferaseInsulin resistanceOxidative stressProtein carbonylationReactive oxygen species

Identifiers

PMID23584148
PMCPMC3769464
OpenAlexW2030074551

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.