Evidence map›Paper›PMID 32292063›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2020

Peroxiredoxin 1 plays a primary role in protecting pancreatic β-cells from hydrogen peroxide and peroxynitrite.

Jennifer S Stancill, John T Happ, Katarzyna A Broniowska, Neil Hogg, John A Corbett

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.3field-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

32 citing papers in PubMed, 69 citations in OpenAlex.

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  15. Anti-Oxidative Therapy in Islet Cell Transplantation.Antioxidants (Basel, Switzerland) · 2022
    Review
  16. Article
  17. Review
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  19. Review
  20. Antioxidants-Related Superoxide Dismutase (Antioxidants (Basel, Switzerland) · 2021
    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

5 authors at 1 institution in 1 country.

Jennifer S StancillDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin.
John T HappDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin.
Katarzyna A BroniowskaDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin.
Neil HoggDepartment of Biophysics, Medical College of Wisconsin, Milwaukee, Wisconsin.
John A CorbettDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, Wisconsin.
Medical College of Wisconsin · US

Funding

ZONISMIDE IN THE TREATMENT OF SEIZURES IN PATIENTSM01RR000058 · NCRR · MEDICAL COLLEGE OF WISCONSIN · PI DUNN, MICHAEL J · 1985 to 2006
$19.9M
BIOCHEMICAL MECHANISM OF BETA-CELL DESTRUCTIONR01DK052194 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CORBETT, JOHN A · 1998 to 2025
$8.8M
MECHANISMS OF VIRAL INDUCED BETA CELL DAMAGER01AI044458 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CORBETT, JOHN A · 1998 to 2024
$7.5M
Training in Signature Transdisciplinary Cardiovascular SciencesT32HL134643 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Justin L Grobe, Jacquelyn P Kulinski · 2017 to 2026
$4.2M
NCRR NIH HHS M01 RR000058NHLBI NIH HHS T32 HL134643NIAID NIH HHS R01 AI044458NIDDK NIH HHS R01 DK052194
6 · The paper itself

Abstract

Both reactive nitrogen and oxygen species (RNS and ROS), such as nitric oxide, peroxynitrite, and hydrogen peroxide, have been implicated as mediators of pancreatic β-cell damage during the pathogenesis of autoimmune diabetes. While β-cells are thought to be vulnerable to oxidative damage due to reportedly low levels of antioxidant enzymes, such as catalase and glutathione peroxidase, we have shown that they use thioredoxin reductase to detoxify hydrogen peroxide. Thioredoxin reductase is an enzyme that participates in the peroxiredoxin antioxidant cycle. Peroxiredoxins are expressed in β-cells and, when overexpressed, protect against oxidative stress, but the endogenous roles of peroxiredoxins in the protection of β-cells from oxidative damage are unclear. Here, using either glucose oxidase or menadione to continuously deliver hydrogen peroxide, or the combination of dipropylenetriamine NONOate and menadione to continuously deliver peroxynitrite, we tested the hypothesis that β-cells use peroxiredoxins to detoxify both of these reactive species. Either pharmacological peroxiredoxin inhibition with conoidin A or specific depletion of cytoplasmic peroxiredoxin 1 (

Indexed as

DNA DamageAnimalsCell DeathCell Line, TumorCytoplasmCytoprotectionEnzyme InhibitorsHydrogen PeroxideInsulin-Secreting CellsMaleOxidative StressPeroxiredoxinsPeroxynitrous AcidQuinoxalinesRats, Sprague-DawleyRNA Interferenceconoidin AEnzyme InhibitorsHydrogen PeroxidePeroxiredoxinsPeroxynitrous AcidPrdx1 protein, ratQuinoxalinesRNA, Small InterferingThioredoxin Reductase 1Txnrd1 protein, rathydrogen peroxideoxidative stressperoxiredoxinperoxynitritereactive oxygen speciesβ-cell

Identifiers

PMID32292063
PMCPMC7272767
OpenAlexW3015443730

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.