Evidence map›Paper›PMID 24425761›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2014

Effects of insulin resistance on skeletal muscle growth and exercise capacity in type 2 diabetic mouse models.

Joseph E Ostler, Santosh K Maurya, Justin Dials, Steve R Roof, Steven T Devor, Mark T Ziolo, Muthu Periasamy

Abstract readComparative Study
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Experimental models in diabetes research.Laboratory animal research · 2026
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  8. Sexual dimorphism in animal models of heart failure with preserved ejection fraction.Journal of applied physiology (Bethesda, Md. : 1985) · 2025
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  11. Single-Cell RNA Sequencing Shows Exercise ProtectsJournal of diabetes research · 2025
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  12. Mitigation of high-fat diet-induced sarcopenia byFood science and biotechnology · 2025
    Article
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  15. Article
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  17. Transplanting old organs promotes senescence in young recipients.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2024
    Article
  18. Article
  19. Ubiquitin Proteasome System Role in Diabetes-Induced Cardiomyopathy.International journal of molecular sciences · 2023
    Article
  20. Review

6 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Joseph E OstlerDepartment of Physiology and Cell Biology, The Ohio State University College of Medicine, Columbus, Ohio; and.
Santosh K Maurya
Justin Dials
Steve R Roof
Steven T Devor
Mark T Ziolo
Muthu Periasamy
The Ohio State University · US

Funding

Mechanisms regulating SR Ca2+ ATPase in the AtriaR01HL088555 · NHLBI · OHIO STATE UNIVERSITY · PI PERIASAMY, MUTHU · 2008 to 2012
$1.9M
NHLBI NIH HHS R01-HL-088555
6 · The paper itself

Abstract

Type 2 diabetes mellitus is associated with an accelerated muscle loss during aging, decreased muscle function, and increased disability. To better understand the mechanisms causing this muscle deterioration in type 2 diabetes, we assessed muscle weight, exercise capacity, and biochemistry in db/db and TallyHo mice at prediabetic and overtly diabetic ages. Maximum running speeds and muscle weights were already reduced in prediabetic db/db mice when compared with lean controls and more severely reduced in the overtly diabetic db/db mice. In contrast to db/db mice, TallyHo muscle size dramatically increased and maximum running speed was maintained during the progression from prediabetes to overt diabetes. Analysis of mechanisms that may contribute to decreased muscle weight in db/db mice demonstrated that insulin-dependent phosphorylation of enzymes that promote protein synthesis was severely blunted in db/db muscle. In addition, prediabetic (6-wk-old) and diabetic (12-wk-old) db/db muscle exhibited an increase in a marker of proteasomal protein degradation, the level of polyubiquitinated proteins. Chronic treadmill training of db/db mice improved glucose tolerance and exercise capacity, reduced markers of protein degradation, but only mildly increased muscle weight. The differences in muscle phenotype between these models of type 2 diabetes suggest that insulin resistance and chronic hyperglycemia alone are insufficient to rapidly decrease muscle size and function and that the effects of diabetes on muscle growth and function are animal model-dependent.

Indexed as

Disease Models, AnimalInsulin ResistanceMuscle DevelopmentAnimalsAnimals, Outbred StrainsDiabetes Mellitus, Type 2Hypoglycemic AgentsInsulinMaleMiceMice, Inbred C57BLMice, Mutant StrainsMotor ActivityMuscle, SkeletalPhosphorylationPhysical EnduranceHypoglycemic AgentsInsulinProteasome Endopeptidase Complexsarcopeniaubiquitin

Identifiers

PMID24425761
PMCPMC3948983
OpenAlexW2047831763

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.