Evidence map›Paper›PMID 33147493›Full record

ArticleToxicology and applied pharmacology2020

Arsenic induced redox imbalance triggers the unfolded protein response in the liver of zebrafish.

Patrice Delaney, Anjana Ramdas Nair, Catherine Palmer, Nouf Khan, Kirsten C Sadler

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Effect of Gentianella acuta (Michx.) Hulten against the arsenic-induced development hindrance of mouse oocytes.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2024
    Article
  4. Article
  5. Methods to Study Liver Disease Using Zebrafish Larvae.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. Article
  7. 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

5 authors at 1 institution in 1 country.

Patrice DelaneyProgram in Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates.
Anjana Ramdas NairProgram in Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates.
Catherine PalmerProgram in Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates.
Nouf KhanProgram in Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates.
Kirsten C SadlerProgram in Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates. Electronic address: kirsten.edepli@nyu.edu.
New York University Abu Dhabi · AE

Funding

Understanding fatty liver disease using the zebrafish mutant, foie grasR01AA018886 · NIAAA · NEW YORK UNIVERSITY · PI SADLER EDEPLI, KIRSTEN C · 2009 to 2017
$2.4M
NIAAA NIH HHS R01 AA018886
6 · The paper itself

Abstract

Inorganic arsenic (iAs) is one of the most endemic toxicants worldwide and oxidative stress is a key cellular pathway underlying iAs toxicity. Other cellular stress response pathways, such as the unfolded protein response (UPR), are also impacted by iAs exposure, however it is not known how these pathways intersect to cause disease. We optimized the use of zebrafish larvae to identify the relationship between these cellular stress response pathways and arsenic toxicity. We found that the window of iAs susceptibility during zebrafish development corresponds with the development of the liver, and that even a 24-h exposure can cause lethality if administered to mature larvae, but not to early embryos. Acute exposure of larvae to iAs generates reactive oxygen species (ROS), an antioxidant response, endoplasmic reticulum (ER) stress and UPR activation in the liver. An in vivo assay using transgenic larvae expressing a GFP-tagged secreted glycoprotein in hepatocytes (Tg(fabp10a:Gc-EGFP)) revealed acute iAs exposure selectively decreased expression of Gc-EGFP, indicating that iAs impairs secretory protein folding in the liver. The transcriptional output of UPR activation is preceded by ROS production and activation of genes involved in the oxidative stress response. These studies implicate redox imbalance as the mechanism of iAs-induced ER stress and suggest that crosstalk between these pathways underlie iAs-induced hepatic toxicity.

Indexed as

AnimalsAnimals, Genetically ModifiedAntioxidantsArsenicEndoplasmic Reticulum StressHepatocytesLarvaLiverOxidation-ReductionOxidative StressReactive Oxygen SpeciesSignal TransductionUnfolded Protein ResponseZebrafishAntioxidantsArsenicReactive Oxygen SpeciesArsenicER stressLiverOxidative stressUnfolded protein responseZebrafish

Identifiers

PMID33147493
PMCPMC7725916
OpenAlexW3095042922

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.