Evidence map›Paper›PMID 23283108›Full record

ArticleThe World Allergy Organization journal2012

In vitro effects of Beta-2 agonists on skeletal muscle differentiation, hypertrophy, and atrophy.

Francesca Wannenes, Loretta Magni, Matteo Bonini, Ivan Dimauro, Daniela Caporossi, Costanzo Moretti, Sergio Bonini

Open access · greenAbstract read
In one paragraph

Article in The World Allergy Organization journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. BetaThe Journal of physiology · 2018
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  4. The Effect ofAntioxidants (Basel, Switzerland) · 2024
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  7. Suppression of FoxO1 mRNA by βFEBS open bio · 2022
    Article
  8. Article
  9. Response of the porcineBiochemistry and biophysics reports · 2021
    Article
  10. Article
  11. Article
  12. βAnimal cells and systems · 2019
    Article
  13. Article
  14. α-Ketoglutarate prevents skeletal muscle protein degradation and muscle atrophy through PHD3/ADRB2 pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    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 at 1 institution in 1 country.

Francesca Wannenes1Institute of Translational Pharmacology, National Research Council, Rome, Italy 2Department of Medicine, "Sapienza" University, Rome, Italy 3Department of Health Science, University of Rome 'Foro Italico', Rome, Italy 4Department of Internal Medicine, Endocrinology Unit, University of Tor Vergata, Rome, Italy 5Department of Internal Medicine, Second University of Naples, Naples, Italy.
Loretta Magni
Matteo Bonini
Ivan Dimauro
Daniela Caporossi
Costanzo Moretti
Sergio Bonini
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background: Beta-2 agonists are widely used in the treatment of asthma and chronic obstructive pulmonary disease for their effect on airway smooth muscle relaxation. They also act on skeletal muscle, although their reported ergogenic effect is controversial.

aim: To evaluate the in vitro effects of short-acting and long-acting beta-2 agonists on adrenergic receptor (ADR) expression, hypertrophy, and atrophy markers, in a skeletal muscle cell line.

methods: The C2C12 cell line was used as a model of skeletal muscle differentiation. ADR messenger RNA expression was evaluated in proliferating myoblasts, committed cells, and differentiated myotubes, in basal conditions and after treatment with 10 M clenbuterol, salbutamol, salmeterol, and formoterol. Effect of beta-2 agonists on gene and protein expression of hypertrophy and atrophy markers was assessed in differentiated myotubes.

results: Our study shows that beta-2 ADR messenger RNA was expressed and progressively increased during cell differentiation. Beta-2 agonist treatment did not affect its expression. Skeletal muscle hypertrophy markers (fast and slow myosin, myogenin) were not modulated by any of the beta-2 agonists evaluated. However, clenbuterol induced a significant, dose-dependent downregulation of skeletal muscle atrophy genes (atrogin-1, MuRF-1, and cathepsin L).

conclusions: The reported ergogenic effect of beta-2 agonists, if any, should be considered as drug-specific and not class-specific and that of clenbuterol is mediated by the inhibition of the atrophic pathway.

Identifiers

PMID23283108
PMCPMC3651181
OpenAlexW1556393667

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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.