Evidence map›Paper›PMID 35927269›Full record

Articlenpj aging2022

Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice.

Michel Bernier, Ignacio Navas Enamorado, Mari Carmen Gómez-Cabrera, Miguel Calvo-Rubio, Jose Antonio González-Reyes, Nathan L Price, Ana Belén Cortés-Rodríguez, Juan Carlos Rodríguez-Aguilera, Sandra Rodríguez-López, Sarah J Mitchell and 10 more

Open access · hybridAbstract read
In one paragraph

Article in npj aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

20 authors at 6 institutions in 2 countries.

Michel Bernier *Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Ignacio Navas Enamorado *Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.ORCID http://orcid.org/0000-0003-2197-2864
Mari Carmen Gómez-Cabrera *Freshage Research Group, Department of Physiology, Faculty of Medicine, University of Valencia, and CIBERFES, Fundación Investigación Hospital Clínico Universitario/INCLIVA, Valencia, Spain.ORCID http://orcid.org/0000-0003-4000-1684
Miguel Calvo-RubioTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Jose Antonio González-ReyesDepartamento de Biología Celular, Fisiología e Inmunología, Campus de Excelencia Internacional Agroalimentario, ceiA3, Universidad de Córdoba, Campus de Rabanales, Edificio Severo Ochoa, 3ª planta, 14014, Córdoba, Spain.ORCID http://orcid.org/0000-0003-1918-5490
Nathan L PriceTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Ana Belén Cortés-RodríguezServicio de Fisiopatología Celular y Bioenergética, Universidad Pablo de Olavide, Sevilla, 41013, Spain.
Juan Carlos Rodríguez-AguileraServicio de Fisiopatología Celular y Bioenergética, Universidad Pablo de Olavide, Sevilla, 41013, Spain.
Sandra Rodríguez-LópezDepartamento de Biología Celular, Fisiología e Inmunología, Campus de Excelencia Internacional Agroalimentario, ceiA3, Universidad de Córdoba, Campus de Rabanales, Edificio Severo Ochoa, 3ª planta, 14014, Córdoba, Spain.ORCID http://orcid.org/0000-0002-5088-6458
Sarah J MitchellTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Kelsey N MurtTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Krystle KalafutTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Katrina M WilliamsDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.ORCID http://orcid.org/0000-0003-3729-0630
Christopher W WardDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
Joseph P StainsDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
Gloria Brea-CalvoCentro Andaluz de Biología del Desarrollo and CIBERER, Instituto de Salud Carlos III, Universidad Pablo de Olavide - CSIC - JA, Sevilla, 41013, Spain.ORCID http://orcid.org/0000-0001-5536-6868
Jose M VillalbaDepartamento de Biología Celular, Fisiología e Inmunología, Campus de Excelencia Internacional Agroalimentario, ceiA3, Universidad de Córdoba, Campus de Rabanales, Edificio Severo Ochoa, 3ª planta, 14014, Córdoba, Spain.ORCID http://orcid.org/0000-0001-8554-3802
Sonia Cortassa *Laboratory of Cardiovascular Science, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.
Miguel A Aon *Translational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA.ORCID http://orcid.org/0000-0002-4355-5431
Rafael de CaboTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD, 21224, USA. deCaboRa@grc.nia.nih.gov.ORCID http://orcid.org/0000-0002-3354-2442
National Institute on Aging · USUniversity of Córdoba · ESUniversity of Maryland, Baltimore · USUniversidad Pablo de Olavide · ESInstituto de Salud Carlos III · ESUniversitat de València · ES

Funding

Chemo-mechanical signaling in atrial myocytesR01HL142290 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI LEDERER, WILLIAM JONATHAN, WARD, CHRISTOPHER WILLIAM · 2019 to 2022
$2.6M
Microtubule Regulated Mechanotransduction in Skeletal MuscleR01AR071618 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI WARD, CHRISTOPHER WILLIAM · 2017 to 2021
$2.6M
Osteocyte CaMKII as a Critical Regulator of Bone Physiology and AnabolismR01AR071614 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Joseph P. Stains · 2018 to 2026
$2.6M
NHLBI NIH HHS R01 HL142290NIAMS NIH HHS R01 AR071614NIAMS NIH HHS R01 AR071618
6 · The paper itself

Abstract

Skeletal muscle adapts to different exercise training modalities with age; however, the impact of both variables at the systemic and tissue levels is not fully understood. Here, adult and old C57BL/6 male mice were assigned to one of three groups: sedentary, daily high-intensity intermittent training (HIIT), or moderate intensity continuous training (MICT) for 4 weeks, compatible with the older group's exercise capacity. Improvements in body composition, fasting blood glucose, and muscle strength were mostly observed in the MICT old group, while effects of HIIT training in adult and old animals was less clear. Skeletal muscle exhibited structural and functional adaptations to exercise training, as revealed by electron microscopy, OXPHOS assays, respirometry, and muscle protein biomarkers. Transcriptomics analysis of gastrocnemius muscle combined with liver and serum metabolomics unveiled an age-dependent metabolic remodeling in response to exercise training. These results support a tailored exercise prescription approach aimed at improving health and ameliorating age-associated loss of muscle strength and function in the elderly.

Identifiers

PMID35927269
PMCPMC9237062
OpenAlexW4283574891

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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.