Evidence mapPaperPMID 39334732Full record

ArticleAntioxidants (Basel, Switzerland)2024

Challenging Sarcopenia: Exploring AdipoRon in Aging Skeletal Muscle as a Healthspan-Extending Shield.

Camille M Selvais, Maria A Davis-López de Carrizosa, Romain Versele, Nicolas Dubuisson, Laurence Noel, Sonia M Brichard, Michel Abou-Samra

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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.

Camille M SelvaisEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.
Maria A Davis-López de CarrizosaEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0002-2551-3115
Romain VerseleEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0001-6096-3122
Nicolas DubuissonEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0003-4258-0579
Laurence NoelEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.
Sonia M BrichardEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.
Michel Abou-SamraEndocrinology, Diabetes and Nutrition Unit, Institute of Experimental and Clinical Research, UCLouvain, 1200 Brussels, Belgium.

Funding

from Société Francophone du Diabète/Abott Diabetes Care 2020 N/AFund for Scientific Research- FNRS 35275437
6 · The paper itself

Abstract

Sarcopenia, characterized by loss of muscle mass, quality, and function, poses significant risks in aging. We previously demonstrated that long-term treatment with AdipoRon (AR), an adiponectin receptor agonist, alleviated myosteatosis and muscle degeneration in middle-aged obese mice. This study aimed to determine if a shorter AR treatment could effectively offset sarcopenia in older mice. Two groups of old mice (20-23 months) were studied, one untreated (O) and one orally-treated with AR (O-AR) at 50 mg/kg/day for three months, compared with control 3-month-old young mice (Y) or 10-month-old young-adult mice (C-10). Results showed that AR remarkably inversed the loss of muscle mass by restoring the sarcopenia index and fiber count, which were greatly diminished with age. Additionally, AR successfully saved muscle quality of O mice by halving the accumulation of tubular aggregates and aberrant mitochondria, through AMPK pathway activation and enhanced autophagy. AR also bolstered muscle function by rescuing mitochondrial activity and improving exercise endurance. Finally, AR markedly curbed muscle fibrosis and mitigated local/systemic inflammation. Thus, a late three-month AR treatment successfully opposed sarcopenia and counteracted various hallmarks of aging, suggesting AR as a promising anti-aging therapy for skeletal muscles, potentially extending healthspan.

Indexed as

abnormal mitochondriaadiponectinadiponectin agonistAMPKautophagysarcopeniatubular aggregates

Identifiers

PMID39334732
PMCPMC11428238

What Socratic 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 Socratic graph.