Evidence map›Paper›PMID 25031153›Full record

ArticleHeart and vessels2015

Oxidation-induced loss of the ability of HDL to counteract the inhibitory effect of oxidized LDL on vasorelaxation.

Laurence Perségol, Marie-Claude Brindisi, David Rageot, Jean-Paul Pais de Barros, Serge Monier, Bruno Vergès, Laurence Duvillard

Abstract read
PubMed Publisher
In one paragraph

Article in Heart and vessels, 2015. 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
0.6field-weighted citation impact, top 38% 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, 11 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Laurence PerségolFaculté de Médecine, INSERM U866-Université de Bourgogne, 21000, Dijon, France.
Marie-Claude BrindisiFaculté de Médecine, INSERM U866-Université de Bourgogne, 21000, Dijon, France.
David RageotPlateforme Lipidomique, Structure Fédérative de Recherche, 21000, Dijon, France.
Jean-Paul Pais de BarrosPlateforme Lipidomique, Structure Fédérative de Recherche, 21000, Dijon, France.
Serge MonierFaculté de Médecine, INSERM U866-Université de Bourgogne, 21000, Dijon, France.
Bruno VergèsFaculté de Médecine, INSERM U866-Université de Bourgogne, 21000, Dijon, France.
Laurence DuvillardFaculté de Médecine, INSERM U866-Université de Bourgogne, 21000, Dijon, France. laurence.duvillard@chu-dijon.fr.
Centre de recherche Translationnelle en Médecine moléculaire · FRInserm · FRUniversité de Bourgogne · FRCentre Hospitalier Universitaire Dijon Bourgogne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several current diseases are associated with an increase in the oxidation of HDL, which is likely to impair their functionality. Our aim was to identify whether oxidation could change the protective effect of HDL against the deleterious effect on vasoreactivity induced by oxidative stress. HDL from healthy subjects were oxidized in vitro by Cu(2+), and the ability of oxidized HDL to counteract the inhibitory effect of oxidized LDL on acetylcholine-induced vasodilation was tested on isolated rabbit aorta rings. Oxidation of HDL was evidenced by the increase in the 7-oxysterols/cholesterol ratio (3.20 ± 1.12 vs 0.02 ± 0.01 % in native HDL, p < 0.05). Oxidized LDL inhibited endothelium-dependent vasodilation (E max = 50.2 ± 5.0 vs 92.5 ± 1.7 % for incubation in Kreb's buffer, p < 0.05) and native HDL counteracted this inhibition (E max = 72.4 ± 4.8 vs 50.2 ± 5.0 % p < 0.05). At the opposite, oxidized HDL had no effect on oxidized LDL-induced inhibition on endothelium-dependent vasorelaxation (E max = 53.7 ± 4.8 vs 50.2 ± 5.0 %, NS). HDL oxidation is associated with a decreased ability of HDL to remove 7-oxysterols from oxidized LDL. In conclusion, these results show that oxidation of HDL induces the loss of their protective effect against endothelial dysfunction, which could promote atherosclerosis in diseases associated with increased oxidative stress.

Indexed as

AcetylcholineAnimalsAortaFemaleHumansIn Vitro TechniquesLipoproteins, HDLLipoproteins, LDLMaleMiddle AgedOxidative StressRabbitsVasodilationAcetylcholineLipoproteins, HDLLipoproteins, LDLoxidized low density lipoproteinOxidized HDLOxidized LDLRabbit aorta ringsVasorelaxation

Identifiers

PMID25031153
OpenAlexW2034802126

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.