Evidence map›Paper›PMID 28611668›Full record

ArticleFrontiers in pharmacology2017

Selective Tissue Distribution Mediates Tissue-Dependent PPARγ Activation and Insulin Sensitization by INT131, a Selective PPARγ Modulator.

Xinni Xie, Wei Chen, Ning Zhang, Mei Yuan, Cheng Xu, Zhibing Zheng, Hua Li, Lili Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 12 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 2 institutions in 1 country.

Xinni XieBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Wei ChenBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Ning ZhangBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Mei YuanBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Cheng XuSchool of Pharmaceutical Engineering, Life Science and Biology Pharmacy College, Shenyang Pharmaceutical UniversityShenyang, China.
Zhibing ZhengBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Hua LiBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Lili WangBeijing Institute of Pharmacology and ToxicologyBeijing, China.
Chinese Academy of Sciences · CNShenyang Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanisms underlying the enhancement of insulin sensitivity by selective peroxisome proliferator-activated receptor γ modulators (sPPARγMs) are still not completely known. Here, the representative sPPARγM, INT131, was used as a probe to investigate the insulin-sensitizing mechanisms of sPPARγM in the context of tissue selective compound distribution and PPARγ regulation. First, 30 mg kg

Indexed as

insulin sensitivityINT131PPARγselective PPARγ modulatortissue distribution

Identifiers

PMID28611668
PMCPMC5447729
OpenAlexW2618503376

What OpenQuestion holds

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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.