Evidence map›Paper›PMID 34506109›Full record

ArticleChemical research in toxicology2021

Characterization of Catecholaldehyde Adducts with Carnosine and l-Cysteine Reveals Their Potential as Biomarkers of Catecholaminergic Stress.

Rachel A Crawford, Ettore Gilardoni, T Blake Monroe, Luca Regazzoni, Ethan J Anderson, Jonathan A Doorn

Abstract read
In one paragraph

Article in Chemical research in toxicology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Role of cytokines and reactive oxygen species in brain aging.Mechanisms of ageing and development · 2023
    Review
  5. Article
  6. 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

6 authors.

Rachel A CrawfordDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, 180 South Grand Avenue, Iowa City, Iowa 52242, United States.
Ettore GilardoniDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, 180 South Grand Avenue, Iowa City, Iowa 52242, United States.
T Blake MonroeDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, 180 South Grand Avenue, Iowa City, Iowa 52242, United States.
Luca RegazzoniDepartment of Pharmaceutical Sciences, University of Milan, Via L. Mangiagalli 25, Milan 20133, Italy.ORCID 0000-0001-7199-7141
Ethan J AndersonDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, 180 South Grand Avenue, Iowa City, Iowa 52242, United States.
Jonathan A DoornDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, 180 South Grand Avenue, Iowa City, Iowa 52242, United States.ORCID 0000-0001-9646-9871

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
Predoctoral Training in the Pharmacological SciencesT32GM067795 · NIGMS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2004 to 2021
$3.4M
Myocardial redox status, catecholamine metabolism and post-operative arrhythmiaR01HL122863 · NHLBI · UNIVERSITY OF IOWA · PI ANDERSON, ETHAN JOHN · 2014 to 2018
$2.1M
Pesticide-Mediated Generation of a Toxic Neurotransmitter MetaboliteR01ES029035 · NIEHS · UNIVERSITY OF IOWA · PI DOORN, JONATHAN A · 2018 to 2022
$1.9M
Toxic neurotransmitter metabolites in aged and diabetic human myocardiumR21AG057006 · NIA · UNIVERSITY OF IOWA · PI ANDERSON, ETHAN JOHN, DOORN, JONATHAN A · 2017 to 2018
$419k
NHLBI NIH HHS R01 HL122863NIA NIH HHS R21 AG057006NIEHS NIH HHS P30 ES005605NIEHS NIH HHS R01 ES029035NIGMS NIH HHS T32 GM067795
6 · The paper itself

Abstract

Monoamine oxidase (MAO) catalyzes the oxidative deamination of dopamine and norepinephrine to produce 3,4-dihydroxyphenylacetaldehyde (DOPAL) and 3,4-dihydroxyphenylglycolaldehyde (DOPEGAL), respectively. Both of these aldehydes are potently cytotoxic and have been implicated in pathogenesis of neurodegenerative and cardiometabolic disorders. Previous work has demonstrated that both the catechol and aldehyde moieties of DOPAL are reactive and cytotoxic via their propensity to cause macromolecular cross-linking. With certain amines, DOPAL likely reacts via a Schiff base before oxidative activation of the catechol and rearrangement to a stable indole product. Our current work expands on this reactivity and includes the less-studied DOPEGAL. Although we confirmed that antioxidants mediated DOPAL's reactivity with carnosine and

Indexed as

3,4-Dihydroxyphenylacetic AcidAnimalsBiomarkersCarnosineCatecholsCell Line, TumorCysteineHumansMiceMice, Inbred C57BLMolecular StructureMonoamine Oxidase3,4-dihydroxyphenylacetaldehyde3,4-Dihydroxyphenylacetic AcidBiomarkersCarnosinecatecholCatecholsCysteineMonoamine Oxidase

Identifiers

PMID34506109
PMCPMC8527522

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.