Evidence map›Paper›PMID 20855423›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2010

SKN-1/Nrf2 inhibits dopamine neuron degeneration in a Caenorhabditis elegans model of methylmercury toxicity.

Natalia Vanduyn, Raja Settivari, Garry Wong, Richard Nass

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Mercury Toxicity and Neurogenesis in the Mammalian Brain.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Post-translational modifications in MeHg-induced neurotoxicity.Biochimica et biophysica acta. Molecular basis of disease · 2019
    Review
  19. Article
  20. East Indian sandalwood (RSC advances · 2018
    Article
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

4 authors at 3 institutions in 2 countries.

Natalia VanduynDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Raja Settivari
Garry Wong
Richard Nass
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USUniversity of Eastern Finland · FI

Funding

Molecular Genetics of Manganese Induced Dopamine Neuron ToxicityR01ES014459 · NIEHS · VANDERBILT UNIVERSITY · PI NASS, RICHARD M · 2006 to 2010
$1.5M
NIEHS NIH HHS R011ES014459NIEHS NIH HHS R01 ES014459
6 · The paper itself

Abstract

Methylmercury (MeHg) exposure from occupational, environmental, and food sources is a significant threat to public health. MeHg poisonings in adults may result in severe psychological and neurological deficits, and in utero exposures can confer embryonic defects and developmental delays. Recent epidemiological and vertebrate studies suggest that MeHg exposure may also contribute to dopamine (DA) neuron vulnerability and the propensity to develop Parkinson's disease (PD). In this study, we describe a Caenorhabditis elegans model of MeHg toxicity that shows that low, chronic exposure confers embryonic defects, developmental delays, decreases in brood size and animal viability, and DA neuron degeneration. Toxicant exposure results in the robust induction of the glutathione-S-transferases (GSTs) gst-4 and gst-38 that are largely dependent on the PD-associated phase II antioxidant transcription factor SKN-1/Nrf2. We also demonstrate that the expression of SKN-1, a protein previously localized to a small subset of chemosensory neurons and intestinal cells in the nematode, is also expressed in the DA neurons, and a reduction in SKN-1 gene expression increases MeHg-induced animal vulnerability and DA neuron degeneration. These studies recapitulate fundamental hallmarks of MeHg-induced mammalian toxicity, identify a key molecular regulator of toxicant-associated whole-animal and DA neuron vulnerability, and suggest that the nematode will be a useful in vivo tool to identify and characterize mediators of MeHg-induced developmental and DA neuron pathologies.

Indexed as

AnimalsAnimal Testing AlternativesCaenorhabditis elegansCaenorhabditis elegans ProteinsDisease Models, AnimalDNA-Binding ProteinsDopamineEmbryo, NonmammalianLarvaLongevityMercury Poisoning, Nervous SystemMethylmercury CompoundsNerve DegenerationNeuronsNF-E2-Related Factor 2ReproductionCaenorhabditis elegans ProteinsDNA-Binding ProteinsDopaminemethylmercuric chlorideMethylmercury CompoundsNF-E2-Related Factor 2skn-1 protein, C elegansTranscription FactorsWater Pollutants, Chemical

Identifiers

PMID20855423
PMCPMC3003544
OpenAlexW2114802579

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.