Evidence map›Paper›PMID 29269872›Full record

ArticleNutrition & diabetes2017

The monounsaturated fatty acid oleate is the major physiological toxic free fatty acid for human beta cells.

T Plötz, B Krümmel, A Laporte, A Pingitore, S J Persaud, A Jörns, M Elsner, I Mehmeti, S Lenzen

Open access · goldAbstract read
In one paragraph

Article in Nutrition & diabetes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 50 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 3 institutions in 2 countries.

T PlötzInstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany.
B KrümmelInstitute of Experimental Diabetes Research, Hannover Medical School, Hannover, Germany.ORCID 0000-0003-4600-9660
A LaporteInstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany.
A PingitoreDivision of Diabetes and Nutritional Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.ORCID 0000-0002-1194-4280
S J PersaudDivision of Diabetes and Nutritional Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
A JörnsInstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany.
M ElsnerInstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany.
I MehmetiInstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany.
S LenzenInstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany. lenzen.sigurd@mh-hannover.de.
Medizinische Hochschule Hannover · DEKing's College London · GBUniversitätsmedizin Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Free fatty acids (FFAs) can cause glucose intolerance and diabetes. Lipotoxicity to the pancreatic beta cells is considered to be a major underlying cause for this phenomenon. The aim of this study was to analyse the toxicity profile of FFAs in the human EndoC-βH1 beta-cell line and to compare the results with isolated rat and human islets with special reference to the physiologically most prevalent FFAs palmitic acid (PA) and oleic acid (OA). Toxicity after a 2-day incubation with the different FFAs was analysed by the caspase-3 assay and confirmed by the propidium iodide and annexin V staining tests. The long-chain saturated PA (C16:0) and the monounsaturated OA (C18:1) were both toxic to human EndoC-βH1 beta cells and pseudoislets, as well as to rat islets, and, as confirmed in a pilot experiment, also to human islets. Furthermore, OA provided no protection against the toxicity of PA. Likewise, elaidic acid (EA, the trans isomer of OA; trans-OA) was significantly toxic, in contrast to the non-metabolisable analogues methylated PA (MePA) and methylated OA (MeOA). Fatty acids with a chain length  < C16 were not toxic in EndoC-βH1 beta cells. Caspase-3 was also activated by linoleic acid (LA)(C18:2) but not by γ-linolenic acid (γ-LNA)(C18:3). Overall, only long-chain FFAs with chain lengths  > C14, which generate hydrogen peroxide in the peroxisomal beta-oxidation, were toxic. This conclusion is also supported by the toxicity of the branched-chain FFA pristanic acid, which is exclusively metabolised in the peroxisomal beta-oxidation. The lack of a protective effect of the monounsaturated fatty acid OA has important consequences for a beta-cell protective lipid composition of a diet. A cardioprotective diet with a high OA content does not fulfil this requirement.

Indexed as

AnimalsCaspase 3Cell LineFatty Acids, MonounsaturatedHumansInsulin-Secreting CellsOleic AcidPalmitic AcidRatsRats, Inbred LewCaspase 3Fatty Acids, MonounsaturatedOleic AcidPalmitic Acid

Identifiers

PMID29269872
PMCPMC5865546
OpenAlexW2773427144

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.