Evidence map›Paper›PMID 31019294›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2019

Pirfenidone prevents and reverses hepatic insulin resistance and steatohepatitis by polarizing M2 macrophages.

Guanliang Chen, Yinhua Ni, Naoto Nagata, Liang Xu, Fen Zhuge, Mayumi Nagashimada, Shuichi Kaneko, Tsuguhito Ota

Abstract read
PubMed Publisher
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2019. 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
2.6field-weighted citation impact, top 11% 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, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Kynurenine-AhR-SLC39A10-ZnCell communication and signaling : CCS · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Pirfenidone use in fibrotic diseases: What do we know so far?Immunity, inflammation and disease · 2024
    Review
  9. Review
  10. Pirfenidone ameliorates liver steatosis by targeting the STAT3-SCD1 axis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Review
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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.

Guanliang Chen *Advanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.
Yinhua Ni *Advanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.
Naoto NagataAdvanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.ORCID http://orcid.org/0000-0002-2389-2334
Liang XuAdvanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.
Fen ZhugeAdvanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.
Mayumi NagashimadaAdvanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.
Shuichi KanekoAdvanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan.
Tsuguhito OtaAdvanced Preventive Medical Sciences Research Center, Kanazawa University Graduate School of Medical Science, Kanazawa, Ishikawa, 920-8640, Japan. ota@asahikawa-med.ac.jp.
Kanazawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic steatohepatitis (NASH) is associated with lipotoxic liver injury, leading to insulin resistance, inflammation, and fibrosis. Despite its increased global incidence, very few promising treatments for NASH are available. Pirfenidone is an antifibrotic agent used to treat pulmonary fibrosis; it suppresses the pulmonary influx of T cells and macrophages. Here, we investigated the effect of pirfenidone in a mouse model of lipotoxicity-induced NASH via a high-cholesterol and high-fat diet. After 12 weeks of feeding, pirfenidone administration attenuated excessive hepatic lipid accumulation and peroxidation by reducing the expression of genes related to lipogenesis and fatty acid synthesis and enhancing the expression of those related to fatty acid oxidation. Flow cytometry indicated that pirfenidone reduced the number of total hepatic macrophages, particularly CD11c

Indexed as

LiverAnimalsDiet, High-FatDisease Models, AnimalInsulin ResistanceLiver CirrhosisMacrophagesMaleMiceMice, Inbred C57BLNon-alcoholic Fatty Liver DiseaseProtective AgentsPyridonesRAW 264.7 CellspirfenidoneProtective AgentsPyridones

Identifiers

PMID31019294
OpenAlexW2942100664

What OpenQuestion holds

Textmetadata
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.