Evidence map›Paper›PMID 27548151›Full record

ArticleInternational journal of molecular sciences2016

Dextran: Influence of Molecular Weight in Antioxidant Properties and Immunomodulatory Potential.

Vinicius C Soeiro, Karoline R T Melo, Monique G C F Alves, Mayara J C Medeiros, Maria L P M Grilo, Jailma Almeida-Lima, Daniel L Pontes, Leandro S Costa, Hugo A O Rocha

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 54 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

9 authors at 2 institutions in 1 country.

Vinicius C SoeiroDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. vihcampelo@gmail.com.
Karoline R T MeloDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. melo.krt@gmail.com.
Monique G C F AlvesDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. monique.gabi@gmail.com.
Mayara J C MedeirosInstituto de Química (IQ), Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. mayarajane20049@hotmail.com.
Maria L P M GriloDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. mlporpino@hotmail.com.
Jailma Almeida-LimaDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. biolottus23@yahoo.com.br.
Daniel L PontesInstituto de Química (IQ), Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. pontesdl@yahoo.com.
Leandro S CostaDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. leandro-silva-costa@hotmail.com.
Hugo A O RochaDepartamento de Bioquímica, Universidade Federal do Rio Grande do Norte (UFRN), Av. Salgado Filho 3000, Natal-RN 59078-970, Brazil. hugo@cb.ufrn.br.
Universidade Federal do Rio Grande do Norte · BRInstituto Federal do Rio Grande do Norte · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dextrans (α-d-glucans) extracted from Leuconostoc mesenteroides, with molecular weights (MW) of 10 (D10), 40 (D40) and 147 (D147) kDa, were evaluated as antioxidant, anticoagulant and immunomodulatory drugs for the first time. None presented anticoagulant activity. As for the antioxidant and immunomodulatory tests, a specific test showed an increase in the dextran activity that was proportional to the increase in molecular weight. In a different assay, however, activity decreased or showed no correlation to the MW. As an example, the reducing power assay showed that D147 was twice as potent as other dextrans. On the other hand, all three samples showed similar activity (50%) when it came to scavenging the OH radical, whereas only the D10 sample showed sharp activity (50%) when it came to scavenging the superoxide ion. D40 was the single dextran that presented with immunomodulatory features since it stimulated the proliferation (~50%) of murine macrophages (RAW 264.7) and decreased the release of nitric oxide (~40%) by the cells, both in the absence and presence of lipopolysaccharides (LPS). In addition, D40 showed a greater scavenging activity (50%) for the hydrogen peroxide, which caused it to also be the more potent dextran when it came to inhibiting lipid peroxidation (70%). These points toward dextrans with a 40 kDa weight as being ideal for antioxidant and immunomodulatory use. However, future studies with the D40 and other similarly 40 kDa dextrans are underway to confirm this hypothesis.

Indexed as

AnimalsAntioxidantsCell ProliferationDextransLeuconostoc mesenteroidesLipid PeroxidationLipopolysaccharidesMacrophagesMiceMolecular WeightNitric OxideRAW 264.7 CellsAntioxidantsDextransLipopolysaccharidesNitric Oxide40 kDa dextranantioxidant activity">d-glucansimmunomodulatory activityLeuconostoc mesenteroidesα-

Identifiers

PMID27548151
PMCPMC5000737
OpenAlexW2512552184

What OpenQuestion holds

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Registered trials

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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.