Evidence map›Paper›PMID 31354530›Full record

ArticleFrontiers in physiology2019

Metabolic Reprogramming Promotes Myogenesis During Aging.

Roberta Belli, Agnese Bonato, Luciana De Angelis, Simone Mirabilii, Maria Rosaria Ricciardi, Agostino Tafuri, Alessio Molfino, Stefania Gorini, Massimiliano Leigheb, Paola Costelli and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

25 citing papers in PubMed, 30 citations in OpenAlex.

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  17. Effect of Pinoresinol and Vanillic Acid Isolated fromMolecules (Basel, Switzerland) · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

Roberta BelliDepartment of Translational and Precision Medicine (Formerly Department of Clinical Medicine), Sapienza University of Rome, Rome, Italy.
Agnese BonatoInstitute of Cell Biology and Neurobiology, National Research Council (CNR), Rome, Italy.
Luciana De AngelisSAIMLAL, Histology Department, Sapienza University of Rome, Rome, Italy.
Simone MirabiliiHematology, Sant'Andrea University Hospital, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Maria Rosaria RicciardiHematology, Sant'Andrea University Hospital, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Agostino TafuriHematology, Sant'Andrea University Hospital, Department of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Alessio MolfinoDepartment of Translational and Precision Medicine (Formerly Department of Clinical Medicine), Sapienza University of Rome, Rome, Italy.
Stefania GoriniDepartment of Orthopaedics and Traumatology, Hospital "Maggiore della Carità", Università del Piemonte Orientale (UPO), Novara, Italy.
Massimiliano LeighebDepartment of Orthopaedics and Traumatology, Hospital "Maggiore della Carità", Università del Piemonte Orientale (UPO), Novara, Italy.
Paola CostelliDepartment of Clinical and Biological Sciences, University of Turin, Turin, Italy.
Maurizia CarusoInstitute of Cell Biology and Neurobiology, National Research Council (CNR), Rome, Italy.
Maurizio MuscaritoliDepartment of Translational and Precision Medicine (Formerly Department of Clinical Medicine), Sapienza University of Rome, Rome, Italy.
Elisabetta FerraroDepartment of Orthopaedics and Traumatology, Hospital "Maggiore della Carità", Università del Piemonte Orientale (UPO), Novara, Italy.
Sapienza University of Rome · ITInstitute of Cell Biology and Neurobiology · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITIstituto di Ricovero e Cura a Carattere Scientifico San RaffaeleUniversity of Turin · IT

Funding

Ricerca Finalizzata Grant RF-2010-231-8508
6 · The paper itself

Abstract

Sarcopenia is the age-related progressive loss of skeletal muscle mass and strength finally leading to poor physical performance. Impaired myogenesis contributes to the pathogenesis of sarcopenia, while mitochondrial dysfunctions are thought to play a primary role in skeletal muscle loss during aging. Here we studied the link between myogenesis and metabolism. In particular, we analyzed the effect of the metabolic modulator trimetazidine (TMZ) on myogenesis in aging. We show that reprogramming the metabolism by TMZ treatment for 12 consecutive days stimulates myogenic gene expression in skeletal muscle of 22-month-old mice. Our data also reveal that TMZ increases the levels of mitochondrial proteins and stimulates the oxidative metabolism in aged muscles, this finding being in line with our previous observations in cachectic mice. Moreover, we show that, besides TMZ also other types of metabolic modulators (i.e., 5-Aminoimidazole-4-Carboxamide Ribofuranoside-AICAR) can stimulate differentiation of skeletal muscle progenitors

Indexed as

agingmetabolic reprogrammingmetabolismmitochondriamyogenesisneuromuscular activitysarcopeniatrimetazidine

Identifiers

PMID31354530
PMCPMC6636331
OpenAlexW2960144268

What OpenQuestion holds

Textmetadata
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.