Evidence map›Paper›PMID 25962124›Full record

ArticleMarine drugs2015

Astaxanthin from Haematococcus pluvialis Prevents Oxidative Stress on Human Endothelial Cells without Toxicity.

Philippe Régnier, Jorge Bastias, Violeta Rodriguez-Ruiz, Noelia Caballero-Casero, Carmen Caballo, Dolores Sicilia, Axelle Fuentes, Murielle Maire, Michel Crepin, Didier Letourneur and 3 more

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.2field-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

50 citing papers in PubMed, 146 citations in OpenAlex.

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  10. Cells · 2023
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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

13 authors at 6 institutions in 2 countries.

Philippe RégnierINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. philregnier@hotmail.fr.
Jorge BastiasCORDUNAP IBT, Avenida Playa Brava 3256, 1100000 Iquique, Chile. jorge.bastias@cordunap.cl.
Violeta Rodriguez-RuizINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. violeta.rodriguezruiz@univ-paris13.fr.
Noelia Caballero-CaseroDepartment of Analytical Chemistry, Institute of Fine Chemistry and Nanochemistry, Campus of Rabanales, University of Córdoba, 14071 Córdoba, Spain. noelia.caballero.c@gmail.com.
Carmen CaballoDepartment of Analytical Chemistry, Institute of Fine Chemistry and Nanochemistry, Campus of Rabanales, University of Córdoba, 14071 Córdoba, Spain. calic_amb@hotmail.es.
Dolores SiciliaDepartment of Analytical Chemistry, Institute of Fine Chemistry and Nanochemistry, Campus of Rabanales, University of Córdoba, 14071 Córdoba, Spain. qa1sicrm@uco.es.
Axelle FuentesINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. axelle.fuentes@gmail.com.
Murielle MaireINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. murielle.maire@univ-paris13.fr.
Michel CrepinINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. michel.crepin@inserm.fr.
Didier LetourneurINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. didier.letourneur@inserm.fr.
Virginie GueguenINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. virginie.gueguen@univ-paris13.fr.
Soledad RubioDepartment of Analytical Chemistry, Institute of Fine Chemistry and Nanochemistry, Campus of Rabanales, University of Córdoba, 14071 Córdoba, Spain. qa1rubrs@uco.es.
Graciela Pavon-DjavidINSERM U1148, Laboratory for Vascular Translational Science; University Paris 13, PRES Sorbonne Paris Cité 99, Av. Jean-Baptiste Clément, 93430 Villetaneuse, France. graciela.pavon@univ-paris13.fr.
University of Córdoba · ESUniversité Paris Cité · FRLaboratoire de Recherche Vasculaire Translationnelle · FRInserm · FRSorbonne Paris Cité · FRUniversité Sorbonne Paris Nord · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Astaxanthin, a powerful antioxidant, is a good candidate for the prevention of intracellular oxidative stress. The aim of the study was to compare the antioxidant activity of astaxanthin present in two natural extracts from Haematococcus pluvialis, a microalgae strain, with that of synthetic astaxanthin. Natural extracts were obtained either by solvent or supercritical extraction methods. UV, HPLC-DAD and (HPLC-(atmospheric pressure chemical ionization (APCI)+)/ion trap-MS) characterizations of both natural extracts showed similar compositions of carotenoids, but different percentages in free astaxanthin and its ester derivatives. The Trolox equivalent antioxidant capacity (TEAC) assay showed that natural extracts containing esters displayed stronger antioxidant activities than free astaxanthin. Their antioxidant capacities to inhibit intracellular oxidative stress were then evaluated on HUVEC cells. The intracellular antioxidant activity in natural extracts was approximately 90-times higher than synthetic astaxanthin (5 µM). No modification, neither in the morphology nor in the viability, of vascular human cells was observed by in vitro biocompatibility study up to 10 µM astaxanthin concentrations. Therefore, these results revealed the therapeutic potential of the natural extracts in vascular human cell protection against oxidative stress without toxicity, which could be exploited in prevention and/or treatment of cardiovascular diseases.

Indexed as

AntioxidantsCarotenoidsCells, CulturedEndothelial CellsHumansHuman Umbilical Vein Endothelial CellsMicroalgaeOxidative StressXanthophyllsAntioxidantsastaxanthineCarotenoidsXanthophylls

Identifiers

PMID25962124
PMCPMC4446609
OpenAlexW1512929108

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.