Evidence map›Paper›PMID 38892381›Full record

ArticleInternational journal of molecular sciences2024

Longitudinal Analysis of Mitochondrial Function in a Choline-Deficient L-Amino Acid-Defined High-Fat Diet-Induced Metabolic Dysfunction-Associated Steatohepatitis Mouse Model.

Akiko Yamada, Akira Watanabe, Atsushi Nara, Naozumi Ishimaru, Kosuke Maeda, Yusuke Ido, Kazumasa Kotake, Masatake Asano, Yasuo Shinohara, Takenori Yamamoto

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

10 authors.

Akiko YamadaDepartment of Pathology, Nihon University School of Dentistry, Chiyoda-ku, Tokyo 101-8310, Japan.
Akira WatanabeInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.
Atsushi NaraInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.
Naozumi IshimaruDepartment of Oral Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo 113-8549, Japan.ORCID 0000-0003-1087-8338
Kosuke MaedaInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.
Yusuke IdoInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.
Kazumasa KotakeInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.ORCID 0000-0001-9869-1177
Masatake AsanoDepartment of Pathology, Nihon University School of Dentistry, Chiyoda-ku, Tokyo 101-8310, Japan.
Yasuo ShinoharaInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.ORCID 0000-0002-5331-3508
Takenori YamamotoInstitute for Genome Research, Tokushima University, Kuramoto, Tokushima 770-8503, Japan.

Funding

Japan Society for the Promotion of Science 18H02971
6 · The paper itself

Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD) is one of the most common chronic liver diseases worldwide. Some patients with MAFLD develop metabolic dysfunction-associated steatohepatitis (MASH), which can lead to severe liver fibrosis. However, the molecular mechanisms underlying this progression remain unknown, and no effective treatment for MASH has been developed so far. In this study, we performed a longitudinal detailed analysis of mitochondria in the livers of choline-deficient, methionine-defined, high-fat-diet (CDAHFD)-fed mice, which exhibited a MASH-like pathology. We found that FoF

Indexed as

Choline DeficiencyDiet, High-FatDisease Models, AnimalFatty LiverAmino AcidsAnimalsCholineLiver CirrhosisMaleMethionineMiceMice, Inbred C57BLMitochondriaMitochondria, LiverMitochondrial Permeability Transition PoreAmino AcidsCholineMethionineMitochondrial Permeability Transition PoreFoF1–ATPaseliver fibrosismetabolic dysfunction-associated steatohepatitismitochondriapermeability transition

Identifiers

PMID38892381
PMCPMC11173319

What OpenQuestion holds

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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.