Evidence map›Paper›PMID 27493874›Full record

ArticleJournal of cachexia, sarcopenia and muscle2016

Diabetic mice exhibited a peculiar alteration in body composition with exaggerated ectopic fat deposition after muscle injury due to anomalous cell differentiation.

Masaki Mogi, Katsuhiko Kohara, Hirotomo Nakaoka, Harumi Kan-No, Kana Tsukuda, Xiao-Li Wang, Toshiyuki Chisaka, Hui-Yu Bai, Bao-Shuai Shan, Masayoshi Kukida and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

29 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Deletion of Tgf-β1 From CD206Journal of cachexia, sarcopenia and muscle · 2026
    Article
  3. Review
  4. Review
  5. Cellular and molecular mechanisms of fatty infiltration in paraspinal muscles in spine-specific sarcopenia.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  6. Article
  7. PdgfrαGenes & diseases · 2025
    Review
  8. Review
  9. Ucp1 Ablation Improves Skeletal Muscle Glycolytic Function in Aging Mice.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  10. FAPs orchestrate homeostasis of muscle physiology and pathophysiology.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    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

13 authors at 1 institution in 1 country.

Masaki MogiDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Katsuhiko KoharaDepartment of Neurology and Geriatric Medicine Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Hirotomo NakaokaDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Harumi Kan-NoDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Kana TsukudaDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Xiao-Li WangDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Toshiyuki ChisakaDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan; Department of Pediatrics Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Hui-Yu BaiDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Bao-Shuai ShanDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Masayoshi KukidaDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan; Department of Cardiology, Pulmonology, Hypertension and Nephrology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Jun IwanamiDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Tetsuro MikiDepartment of Neurology and Geriatric Medicine Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Masatsugu HoriuchiDepartment of Molecular Cardiovascular Biology and Pharmacology Ehime University, Graduate School of Medicine Tohon Ehime 791-0295 Japan.
Ehime University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSarcopenic obesity, age-related muscle loss, which is compensated by an increase in fat mass, impairs quality of life in elderly people. Although the increase in intramuscular fat is associated with decreased insulin sensitivity and increased metabolic risk factors, the origin of diabetes-associated intramuscular fat has not been elucidated. Here, we investigated intramuscular fat deposition using a muscle injury model in type 2 diabetic mice.

methodsMale 8-week-old C57BL/6 and 8-week-old and 26-week-old KKAy underwent intramuscular injection of cardiotoxin (Ctx) (100 μL/10 μM) into the tibialis anterior (TA) muscles. After 2 weeks, the muscles were removed and evaluated.

resultsKKAy exhibited impaired muscle regeneration and ectopic fat deposition. Such impairment was more marked in older KKAy. These changes were also observed in another diabetic mouse model, db/db and diet-induced obese mice but not in streptozocin-induced diabetic mice. Deposited fat was platelet-derived growth factor (PDGF) receptor alpha positive and its cytoskeleton was stained with Masson's trichrome, indicating it to be of fibro-adipocyte progenitor cell origin. Expression of a myogenic marker, myoD, was lower and that of PDGF receptor alpha and CCAAT/enhancer binding protein (CEBP) alpha was higher in Ctx-injured TA of KKAy compared with that of C57BL/6. Peroxisome proliferator-activated receptor γ (PPARγ) was highly expressed in fat-forming lesions in older KKAy. Treatment with all-trans retinoic acid prevented the formation of intramuscular fat; however, treatment with GW9662, a PPARγ antagonist, increased the fibrotic change in muscle.

conclusionsDiabetic mice showed impaired muscle regeneration with fat deposition, suggesting that diabetes may enhance sarcopenic obesity through a mechanism involving anomalous fibro-adipocyte progenitor cell differentiation.

Indexed as

Diabetes mellitusEctopic fat depositionFibro‐adipocyte progenitor cellMuscle regenerationSarcopenic obesity

Identifiers

PMID27493874
PMCPMC4864245
OpenAlexW1602327320

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.