Evidence map›Paper›PMID 25087485›Full record

ArticleScientific reports2014

Excited singlet molecular O₂(¹Δg) is generated enzymatically from excited carbonyls in the dark.

Camila M Mano, Fernanda M Prado, Júlio Massari, Graziella E Ronsein, Glaucia R Martinez, Sayuri Miyamoto, Jean Cadet, Helmut Sies, Marisa H G Medeiros, Etelvino J H Bechara and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 64 citations in OpenAlex.

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  10. Chemiexcitation: Mammalian Photochemistry in the DarkPhotochemistry and photobiology · 2023
    Review
  11. Review
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  13. Regulation of Ion Channel Function by Gas Molecules.Advances in experimental medicine and biology · 2021
    Review
  14. Findings in redox biology: From HThe Journal of biological chemistry · 2020
    Article
  15. Review
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  17. Article
  18. Synthesis of meso-tetra-(4-sulfonatophenyl) porphyrin (TPPSInternational journal of nanomedicine · 2019
    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

11 authors at 3 institutions in 2 countries.

Camila M ManoDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Fernanda M PradoDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Júlio MassariDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Graziella E RonseinDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Glaucia R MartinezDepartamento de Bioquímica e Biologia Molecular, Setor de Ciências Biológicas, Universidade Federal do Paraná, Curitiba, PR, Brazil.
Sayuri MiyamotoDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Jean CadetInstitut Nanosciences et Cryogénie, CEA/Grenoble, F-38054 Grenoble Cedex 9, France.
Helmut SiesInstitute of Biochemistry and Molecular Biology I, and Leibniz Research Institute for Environmental Medicine, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Marisa H G MedeirosDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Etelvino J H Bechara1] Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil [2] Departamento de Ciências Exatas e da Terra, Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, SP, Brazil.
Paolo Di MascioDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, CEP 05513-970, CP 26077, São Paulo, SP, Brazil.
Universidade de São Paulo · BRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRUniversidade Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In mammalian tissues, ultraweak chemiluminescence arising from biomolecule oxidation has been attributed to the radiative deactivation of singlet molecular oxygen [O2 ((1)Δg)] and electronically excited triplet carbonyl products involving dioxetane intermediates. Herein, we describe evidence of the generation of O2 ((1)Δg) in aqueous solution via energy transfer from excited triplet acetone. This involves thermolysis of 3,3,4,4-tetramethyl-1,2-dioxetane, a chemical source, and horseradish peroxidase-catalyzed oxidation of 2-methylpropanal, as an enzymatic source. Both sources of excited carbonyls showed characteristic light emission at 1,270 nm, directly indicative of the monomolecular decay of O2 ((1)Δg). Indirect analysis of O2 ((1)Δg) by electron paramagnetic resonance using the chemical trap 2,2,6,6-tetramethylpiperidine showed the formation of 2,2,6,6-tetramethylpiperidine-1-oxyl. Using [(18)O]-labeled triplet, ground state molecular oxygen [(18)O2 ((3)Σg(-))], chemical trapping of (18)O2 ((1)Δg) with disodium salt of anthracene-9,10-diyldiethane-2,1-diyl disulfate yielding the corresponding double-[(18)O]-labeled 9,10-endoperoxide, was detected through mass spectrometry. This corroborates formation of O2 ((1)Δg). Altogether, photoemission and chemical trapping studies clearly demonstrate that chemically and enzymatically nascent excited carbonyl generates (18)O2 ((1)Δg) by triplet-triplet energy transfer to ground state oxygen O2 ((3)Σg(-)), and supports the long formulated hypothesis of O2 ((1)Δg) involvement in physiological and pathophysiological events that might take place in tissues in the absence of light.

Indexed as

AcetoneAldehydesDarknessElectron Spin Resonance SpectroscopyHeterocyclic CompoundsHeterocyclic Compounds, 1-RingHorseradish PeroxidaseOxidation-ReductionOxygenSinglet OxygenSolutionsSpin LabelsSpin TrappingWater1,2-dioxetaneAcetoneAldehydesHeterocyclic CompoundsHeterocyclic Compounds, 1-RingHorseradish PeroxidaseisobutyraldehydeOxygenSinglet OxygenSolutionsSpin LabelsWater

Identifiers

PMID25087485
PMCPMC4120373
OpenAlexW2048493057

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.