Evidence mapPaperPMID 38858657Full record

ArticleMolecular medicine (Cambridge, Mass.)2024

The analysis of the skeletal muscle metabolism is crucial for designing optimal exercise paradigms in type 2 diabetes mellitus.

Elias Abi Akar, Laure Weill, Mirella El Khoury, Cédric Caradeuc, Gildas Bertho, Suzan Boutary, Cynthia Bezier, Zoé Clerc, Delphine Sapaly, Sabrina Bendris and 5 more

Abstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

15 authors.

Elias Abi AkarFaculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Laure Weill *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Mirella El Khoury *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Cédric Caradeuc *Faculty of Basic and Biomedical Sciences, Université Paris Cité & UMR8601 CNRS, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Gildas Bertho *Faculty of Basic and Biomedical Sciences, Université Paris Cité & UMR8601 CNRS, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Suzan Boutary *Inserm U1195, Bâtiment Gregory Pincus, 80 rue du Général Leclerc, 94276, Le Kremlin Bicêtre, France.
Cynthia Bezier *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Zoé Clerc *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Delphine Sapaly *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Sabrina Bendris *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Flore Cheguillaume *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Nicolas Giraud *Faculty of Basic and Biomedical Sciences, Université Paris Cité & UMR8601 CNRS, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.
Assaad A EidDepartment of Anatomy, Cell Biology and Physiological Sciences, Faculty of Medicine and Medical Center, American University of Beirut, Bliss Street, 11-0236, Riad El-Solh, Beirut, 1107-2020, Lebanon. ae49@aub.edu.lb.
Frédéric CharbonnierFaculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France. frederic.charbonnier@u-paris.fr.ORCID http://orcid.org/0000-0003-4341-3246
Olivier Biondi *Faculty of Basic and Biomedical Sciences, Université Paris Cité & Inserm UMR_S1124, 45 rue des Saints-Pères, 75270, Paris Cedex 06, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 2 diabetes mellitus (T2DM) is a chronic metabolic disease that commonly results from a high-calorie diet and sedentary lifestyle, leading to insulin resistance and glucose homeostasis perturbation. Physical activity is recommended as one first-line treatment in T2DM, but it leads to contrasted results. We hypothesized that, instead of applying standard exercise protocols, the prescription of personalized exercise programs specifically designed to reverse the potential metabolic alterations in skeletal muscle could result in better results.

methodsTo test this hypothesis, we drew the metabolic signature of the fast-twitch quadriceps muscle, based on a combined unbiased NMR spectroscopy and RT-qPCR study, in several T2DM mouse models of different genetic background (129S1/SvImJ, C57Bl/6J), sex and aetiology (high-fat diet (HFD) or HFD/Streptozotocin (STZ) induction or transgenic MKR (FVB-Tg Ckm-IGF1R*K1003R)1Dlr/J) mice. Three selected mouse models with unique muscular metabolic signatures were submitted to three different swimming-based programs, designed to address each metabolic specificity.

resultsWe found that depending on the genetic background, the sex, and the mode of T2DM induction, specific muscular adaptations occurred, including depressed glycolysis associated with elevated PDK4 expression, shift to β-oxidation, or deregulation of amino-acid homeostasis. Interestingly, dedicated swimming-based exercises designed to restore specific metabolic alterations in muscle were found optimal in improving systemic T2DM hallmarks, including a significant reduction in insulin resistance, the improvement of glucose homeostasis, and a delay in sensorimotor function alterations.

conclusionThe muscle metabolism constitutes an important clue for the design of precision exercises with potential clinical implications for T2DM patients.

Indexed as

Diabetes Mellitus, Type 2Disease Models, AnimalMuscle, SkeletalPhysical Conditioning, AnimalAnimalsDiabetes Mellitus, ExperimentalDiet, High-FatFemaleInsulin ResistanceMaleMetabolomeMetabolomicsMiceMice, Inbred C57BLMice, TransgenicMouse modelsMuscle metabolismPrecision exerciseType 2 diabetes mellitus

Identifiers

PMID38858657
PMCPMC11165837

What Socratic holds

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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 Socratic graph.