Evidence map›Paper›PMID 28086197›Full record

ArticleRedox biology2017

Non-linear impact of glutathione depletion on C. elegans life span and stress resistance.

Nadine Urban, Dimitrios Tsitsipatis, Franziska Hausig, Katrin Kreuzer, Katrin Erler, Vanessa Stein, Michael Ristow, Holger Steinbrenner, Lars-Oliver Klotz

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.9field-weighted citation impact, top 7% 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, 74 citations in OpenAlex.

  1. Review
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  6. Dysfunctional copper homeostasis inRedox biochemistry and chemistry · 2024
    Article
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  9. Review
  10. Potential Therapeutic Effects of Policosanol from Insect Wax on Caenorhabditis elegans Models of Parkinson's Disease.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2023
    Article
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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

9 authors at 2 institutions in 2 countries.

Nadine UrbanInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Dimitrios TsitsipatisInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Franziska HausigInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Katrin KreuzerInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Katrin ErlerInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Vanessa SteinInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Michael RistowETH Zurich (Swiss Federal Institute of Technology), Schorenstrasse 16, Building SLA C7, CH-8603 Schwerzenbach-Zurich, Switzerland.
Holger SteinbrennerInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany.
Lars-Oliver KlotzInstitute of Nutrition, Department of Nutrigenomics, Friedrich-Schiller-Universität Jena, D-07743 Jena, Germany. Electronic address: lars-oliver.klotz@uni-jena.de.
Friedrich Schiller University Jena · DEÉcole Polytechnique Fédérale de Lausanne · CH

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

The redox environment in cells and organisms is set by low-molecular mass and protein-bound thiols, with glutathione (GSH) representing a major intracellular redox buffer. Subtle thiol oxidation elicits signal transduction processes and adaptive responses to cope with stressors, whereas highly oxidizing conditions may provoke cell death. We here tested how thiol depletion affects life span, stress resistance and stress signaling in the model organism Caenorhabditis elegans. Diethyl maleate (DEM), an α,β-unsaturated carbonyl compound that conjugates to GSH and other thiols, decreased C. elegans life span at a concentration of 1mM. In contrast, low and moderate doses of DEM (10-100µM) increased mean and maximum life span and improved resistance against oxidative stress. DEM-induced life span extension was not detectable in worms deficient in either the FoxO orthologue, DAF-16, or the Nrf2 orthologue, SKN-1, pointing to a collaborative role of the two transcription factors in life span extension induced by thiol depletion. Cytoprotective target genes of DAF-16 and SKN-1 were upregulated after at least 3 days of exposure to 100µM DEM, but not 1mM DEM, whereas only 1mM DEM caused upregulation of egl-1, a gene controlled by a p53-orthologue, CEP-1. In order to test whether depletion of GSH may elicit effects similar to DEM, we suppressed GSH biosynthesis in worms by attenuating γ-glutamylcysteine synthetase (gcs-1) expression through RNAi. The decline in GSH levels elicited by gcs-1 knockdown starting at young adult stage did not impair viability, but increased both stress resistance and life expectancy of the worms. In contrast, gcs-1 knockdown commencing right after hatching impaired nematode stress resistance and rendered young adult worms prone to vulval ruptures during egg-laying. Thus, modest decrease in GSH levels in young adult worms may promote stress resistance and life span, whereas depletion of GSH is detrimental to freshly hatched and developing worms.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell DeathDipeptidesDNA-Binding ProteinsForkhead Transcription FactorsGene Expression Regulation, DevelopmentalGene Knockdown TechniquesGlutamate-Cysteine LigaseGlutathioneMaleatesOxidation-ReductionOxidative StressRepressor ProteinsSulfhydryl CompoundsCaenorhabditis elegans ProteinsCEP-1 protein, C elegansdaf-16 protein, C elegansdiethyl maleateDipeptidesDNA-Binding ProteinsEGL-1 protein, C elegansForkhead Transcription Factorsgamma-glutamylcysteineGlutamate-Cysteine LigaseGlutathioneMaleatesRepressor Proteinsskn-1 protein, C elegansSulfhydryl CompoundsTranscription FactorsTumor Suppressor Protein p53AgingC. elegansGlutathioneHormesisStress resistanceThiolγ-glutamylcysteine synthetase

Identifiers

PMID28086197
PMCPMC5228094
OpenAlexW2560708226

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.