Evidence map›Paper›PMID 27348201›Full record

ArticleNutrition & diabetes2016

Eicosapentaenoic acid ameliorates hyperglycemia in high-fat diet-sensitive diabetes mice in conjunction with restoration of hypoadiponectinemia.

M Morimoto, E-Y Lee, X Zhang, Y Inaba, H Inoue, M Ogawa, T Shirasawa, O Yokosuka, T Miki

Open access · goldAbstract read
In one paragraph

Article in Nutrition & diabetes, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 9 citations in OpenAlex.

  1. Bioactive lipids and vascular disease.European journal of clinical nutrition · 2021
    Article
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.

M MorimotoDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.
E-Y LeeDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.
X ZhangDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.
Y InabaMetabolism and Nutrition Research Unit, Innovative Integrated Bio-Research Core, Institute for Frontier Science Initiative, Kanazawa University, Kanazawa, Japan.
H InoueMetabolism and Nutrition Research Unit, Innovative Integrated Bio-Research Core, Institute for Frontier Science Initiative, Kanazawa University, Kanazawa, Japan.
M OgawaDepartment of Gastroenterology and Nephrology, Chiba University, Graduate School of Medicine, Chiba, Japan.
T ShirasawaDepartment of Neurology, University of Michigan, Ann Arbor, MI, USA.
O YokosukaDepartment of Gastroenterology and Nephrology, Chiba University, Graduate School of Medicine, Chiba, Japan.
T MikiDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.
Chiba University · JPKanazawa University · JPUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectiveEicosapentaenoic acid (EPA) exerts pleiotropic effects on metabolic disorders such as atherosclerosis and dyslipidemia, but its effectiveness in the treatment of type 2 diabetes mellitus remains controversial.

methodsWe examined the antidiabetic effect of EPA in insulin receptor mutant (Insr(P1195L/+)) mice that exhibit high-fat diet (HFD)-dependent hyperglycemia.

resultsEPA supplementation was found to alleviate hyperglycemia of Insr(P1195L/+) mice fed HFD (Insr(P1195L/+)/HFD mice), which was accompanied by amelioration of increased gluconeogenesis and impaired insulin signaling, as assessed by glucose-6-phosphatase (G6pc) expression on refeeding and insulin-induced phosphorylation of Akt in the liver, respectively. We found that serum levels of adiponectin, the antidiabetic adipokine, were decreased by HFD along with the body weight gain in Insr(P1195L/+) mice but not in wild-type mice, suggesting that Insr(P1195L/+) mice are prone to hypoadiponectinemia in response to obesity. Interestingly, the blood glucose levels of Insr(P1195L/+) mice were in reverse proportion to their serum adiponectin levels and EPA supplementation ameliorated their hyperglycemia in conjunction with the restoration of hypoadiponectinemia.

conclusionsEPA exerts an antidiabetic effect in Insr(P1195L/+)/HFD mice, an HFD-sensitive, insulin-resistant animal model, possibly through its action against hypoadiponectinemia.

Indexed as

Dietary SupplementsDiet, High-FatAdiponectinAnimalsDiabetes Mellitus, Type 2Disease Models, AnimalEicosapentaenoic AcidHyperglycemiaMaleMetabolism, Inborn ErrorsMicePhosphorylationAdiponectinEicosapentaenoic Acid

Identifiers

PMID27348201
PMCPMC4931313
OpenAlexW2470707497

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.