Evidence map›Paper›PMID 30658644›Full record

ArticleLipids in health and disease2019

A specific combined long-chain polyunsaturated fatty acid supplementation reverses fatty acid profile alterations in a mouse model of chronic asthma.

D Fussbroich, K Zimmermann, A Göpel, O Eickmeier, J Trischler, S Zielen, R Schubert, C Beermann

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

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  8. Dihomo-International journal of molecular sciences · 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

8 authors at 2 institutions in 1 country.

D FussbroichDepartment of Food Technology, University of Applied Science Fulda, Leipziger Str. 123, 36039, Fulda, Germany. daniela.fussbroich@lt.hs-fulda.de.ORCID http://orcid.org/0000-0003-4503-8574
K ZimmermannDepartment of Food Technology, University of Applied Science Fulda, Leipziger Str. 123, 36039, Fulda, Germany.
A GöpelDepartment of Food Technology, University of Applied Science Fulda, Leipziger Str. 123, 36039, Fulda, Germany.
O EickmeierDivision for Allergy, Pneumology and Cystic Fibrosis, Department for Children and Adolescence, Goethe University, Theodor-Stern-Kai 7, Frankfurt/Main, Germany.
J TrischlerDivision for Allergy, Pneumology and Cystic Fibrosis, Department for Children and Adolescence, Goethe University, Theodor-Stern-Kai 7, Frankfurt/Main, Germany.
S ZielenDivision for Allergy, Pneumology and Cystic Fibrosis, Department for Children and Adolescence, Goethe University, Theodor-Stern-Kai 7, Frankfurt/Main, Germany.
R SchubertDivision for Allergy, Pneumology and Cystic Fibrosis, Department for Children and Adolescence, Goethe University, Theodor-Stern-Kai 7, Frankfurt/Main, Germany.
C BeermannDepartment of Food Technology, University of Applied Science Fulda, Leipziger Str. 123, 36039, Fulda, Germany.
Goethe University Frankfurt · DEFulda University of Applied Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe immune-modulating potential of long-chain polyunsaturated fatty acids (LCPUFAs) based on their conversion into lipid mediators in inflammatory situations has been proven by several studies. Respecting the immune-modulative role of lipid mediators in bronchoconstriction, airway inflammation and resolution of inflammatory processes, LCPUFAs play an important role in asthma. To design a disease-specific and most beneficial LCPUFA supplementation strategy, it is essential to understand how asthma alters LCPUFA profiles. Therefore, this study characterizes the alterations of LCPUFA profiles induced by allergic asthma. In addition, this study explores whether a simple eicosapentaenoic acid (EPA) alone or a specific combined LCPUFA supplementation could restore imbalanced LCPUFA profiles.

methodsMice were sensitized with a daily dose of 40 μg house dust mite (HDM)-extract in a recall model and fed with either normal diet, EPA or a specific combined (sc)-LCPUFA supplementation containing EPA, docosahexaenoic acid (DHA), γ -linolenic acid (GLA) and stearidonic acid (SDA) for 24 days. After recall with HDM, mice were sacrificed and blood and lung tissue were collected. Fatty acid profiles were determined in plasma, blood cells and lung cells of asthmatic mice by capillary gas-chromatography.

resultsIn lung cells of asthmatic mice, arachidonic acid (AA, p < 0.001) and DHA (p < 0.01) were increased while dihomo-γ-linolenic acid (DGLA, p < 0.05) was decreased. EPA supplementation increased only EPA (p < 0.001) and docosapentaenoic acid (DPA, p < 0.001), but neither DGLA nor DHA in lung cells of asthmatic mice. In contrast, a specific combined dietary supplementation containing n-3 and n-6 LCPUFAs could decrease AA (p < 0.001), increase EPA (p < 0.001), DPA (p < 0.001) and DHA (p < 0.01) and could reverse the lack of DGLA (p < 0.05).

conclusionsIn summary, allergic asthma alters LCPUFA profiles in blood and lung tissue. In contrast to the EPA supplementation, the distinct combination of n-3 and n-6 LCPUFAs restored the LCPUFA profiles in lung tissue of asthmatic mice completely. Subsequently, sc-LCPUFA supplementation is likely to be highly supportive in limiting and resolving the inflammatory process in asthma.

Indexed as

Dietary SupplementsAnimalsAsthmaChronic DiseaseDisease Models, AnimalEicosapentaenoic AcidFatty AcidsFatty Acids, UnsaturatedFemaleHypersensitivityLungMiceMice, Inbred C57BLEicosapentaenoic AcidFatty AcidsFatty Acids, UnsaturatedAsthmaFatty acid profilesGas-chromatographyLCPUFAOmega-3Omega-6

Identifiers

PMID30658644
PMCPMC6339374
OpenAlexW2912679880

What OpenQuestion holds

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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.