Evidence map›Paper›PMID 27832159›Full record

ArticlePloS one2016

A Novel Selective Inhibitor of Delta-5 Desaturase Lowers Insulin Resistance and Reduces Body Weight in Diet-Induced Obese C57BL/6J Mice.

Hiroaki Yashiro, Shuichi Takagahara, Yumiko Okano Tamura, Ikuo Miyahisa, Junji Matsui, Hideo Suzuki, Shota Ikeda, Masanori Watanabe

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 29 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

8 authors at 1 institution in 1 country.

Hiroaki YashiroPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Shuichi TakagaharaPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Yumiko Okano TamuraPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Ikuo MiyahisaPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Junji MatsuiPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Hideo SuzukiPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Shota IkedaPharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Masanori WatanabePharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa Japan.
Takeda (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is now recognized as a state of chronic low-grade inflammation and is called as metabolic inflammation. Delta-5 desaturase (D5D) is an enzyme that metabolizes dihomo-γ-linolenic acid (DGLA) to arachidonic acid (AA). Thus, D5D inhibition increases DGLA (precursor to anti-inflammatory eicosanoids) while decreasing AA (precursor to pro-inflammatory eicosanoids), and could result in synergistic improvement in the low-grade inflammatory state. Here, we demonstrate reduced insulin resistance and the anti-obesity effect of a D5D selective inhibitor (compound-326), an orally active small-molecule, in a high-fat diet-induced obese (DIO) mouse model. In vivo D5D inhibition was confirmed by determining changes in blood AA/DGLA profiles. In DIO mice, chronic treatment with compound-326 lowered insulin resistance and caused body weight loss without significant impact on cumulative calorie intake. Decreased macrophage infiltration into adipose tissue was expected from mRNA analysis. Increased daily energy expenditure was also observed following administration of compound-326, in line with sustained body weight loss. These data indicate that the novel D5D selective inhibitor, compound-326, will be a new class of drug for the treatment of obese and diabetic patients.

Indexed as

Insulin Resistance8,11,14-Eicosatrienoic AcidAdiponectinAdipose TissueAnimalsArachidonic AcidBody WeightDelta-5 Fatty Acid DesaturaseDiet, High-FatEnergy MetabolismEnzyme InhibitorsFatty Acid DesaturasesFluorocarbonsGene ExpressionHep G2 CellsHumans2-(2,2,3,3,3-pentafluoropropoxy)-3-(4-(2,2,2-trifluoroethoxy)phenyl)-5,7-dihydro-3H-pyrrolo(2,3-d)pyrimidine-4,6-dione8,11,14-Eicosatrienoic AcidAdiponectinArachidonic AcidDelta-5 Fatty Acid DesaturaseEnzyme InhibitorsFatty Acid DesaturasesFluorocarbonsLeptinPyrimidinonesPyrrolidinones

Identifiers

PMID27832159
PMCPMC5104425
OpenAlexW2554533390

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.