Evidence map›Paper›PMID 27576485›Full record

ArticleJournal of the American Society for Mass Spectrometry2016

New Insights on Non-Enzymatic Oxidation of Ganglioside GM1 Using Mass Spectrometry.

Daniela Couto, Tânia Melo, Elisabete Maciel, Ana Campos, Eliana Alves, Sofia Guedes, M Rosário M Domingues, Pedro Domingues

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Biophysical characteristics of lipid-induced Aβ oligomers correlate to distinctive phenotypes in transgenic mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  2. 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

8 authors at 1 institution in 1 country.

Daniela CoutoMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
Tânia MeloMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
Elisabete MacielMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
Ana CamposMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
Eliana AlvesMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
Sofia GuedesMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
M Rosário M DominguesMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal.
Pedro DominguesMass Spectrometry Center, Department of Chemistry and QOPNA, University of Aveiro, 3810-193, Aveiro, Portugal. p.domingues@ua.pt.
University of Aveiro · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gangliosides are acidic glycosphingolipids that are present in cell membranes and lipid raft domains, being particularly abundant in central nervous systems. They participate in modulating cell membrane properties, cell-cell recognition, cell regulation, and signaling. Disturbance in ganglioside metabolism has been correlated with the development of diseases, such as neurodegenerative diseases, and in inflammation. Both conditions are associated with an increased production of reactive oxidation species (ROS) that can induce changes in the structure of biomolecules, including lipids, leading to the loss or modification of their function. Oxidized phospholipids are usually involved in chronic diseases and inflammation. However, knowledge regarding oxidation of gangliosides is scarce. In order to evaluate the effect of ROS in gangliosides, an in vitro biomimetic model system was used to study the susceptibility of GM1 (Neu5Acα2-3(Galβ1-3GalNAcβ1-4)Galβ1-4Glcβ1Cer) to undergo oxidative modifications. Oxidation of GM1 under Fenton reaction conditions was monitored using high resolution electrospray ionization-mass spectrometry (ESI-MS) and tandem mass spectrometry (ESI-MS/MS). Upon oxidation, GM1 underwent oxidative cleavages in the carbohydrate chain, leading to the formation of other gangliosides GM2 (GalNAcβ1-4Gal(Neu5Acα2-3)1-4Glcβ1Cer), GM3 (Neu5Acα2-3Galβ1-4Glcβ1Cer), asialo-GM1 (Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1Cer), asialo-GM2 (GalNAcβ1-4Galβ1-4Glcβ1Cer), of the small glycolipids lactosylceramide (LacCer), glucosylceramide (GlcCer), and of ceramide (Cer). In addition, oxygenated GM1 and GM2 (as keto and hydroxy derivatives), glycans, oxidized glycans, and oxidized ceramides were also identified. Nonenzymatic oxidation of GM1 under oxidative stress contributes to the generation of other gangliosides that may participate in the imbalance of gangliosides metabolism in vivo, through uncontrolled enzymatic pathways and, consequently, play some role in neurodegenerative processes. Graphical Abstract ᅟ.

Indexed as

Electrospray ionizationFenton reactionGM1InflammationNeurodegenerative diseasesReactive oxygen species

Identifiers

PMID27576485
OpenAlexW2518463553

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.