Evidence map›Paper›PMID 35013417›Full record

ArticleScientific reports2022

Different sites of actions make different responses to thiazolidinediones between mouse and rat models of fatty liver.

Chihiro Ebihara, Megumi Aizawa-Abe, Mingming Zhao, Valentino Gumbilai, Ken Ebihara

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
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

5 authors at 2 institutions in 1 country.

Chihiro EbiharaDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Megumi Aizawa-AbeDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mingming ZhaoDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Valentino GumbilaiDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Ken EbiharaDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto, Japan. kebihara@jichi.ac.jp.
Kyoto University · JPJichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic approach for NAFLD is limited and there are no approved drugs. Pioglitazone (PGZ), a thiazolidinedione (TZD) that acts via peroxisome proliferator activated receptor gamma (PPARγ) is the only agent that has shown consistent benefit and efficacy in clinical trials. However, the mechanism of its therapeutic effect on NAFLD remains unclear. The poor understanding may be due to problems with mouse, a species most used for animal experiments. TZDs exacerbate fatty liver in mouse models while they improve it in rat models like in human patients. Therefore, we compared the effects of TZDs including PGZ and rosiglitazone (RGZ) in ob/ob mice and Lep

Indexed as

AnimalsDisease Models, AnimalDrug Evaluation, PreclinicalFatty LiverLeptinLipid MetabolismLipodystrophyMaleMiceMice, Inbred C57BLObesityPioglitazonePPAR gammaRatsRats, TransgenicThiazolidinedionesLeptinPioglitazonePPAR gammaPparg protein, mouseThiazolidinediones

Identifiers

PMID35013417
PMCPMC8748829
OpenAlexW4205851705

What Socratic 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 Socratic graph.