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Regulation of muscle atrophy: wasting away from the outside in: an introduction
1US Army Research Institute of Environmental Medicine, Natick, MA 01760, USA. maria.urso@us.army.mil
Abstract:
Whereas it is clear that periods of detraining, disuse, injury and aging are marked by losses in skeletal muscle mass and function, the emerging literature suggests that there are unique molecular signaling alterations depending on the perturbation. Understanding the phenotypical adaptations in skeletal muscle and factors that are thought to promote or inhibit genes involved in the atrophy program will elucidate how the muscular system responds to decreases in activity. Recent advances in the discipline have identified specific and innovative methods to promote skeletal muscle hypertrophy including gene therapy, pharmacological, and nutritional interventions. The same success has not been met concerning attenuating skeletal muscle atrophy. If novel approaches are to be implemented in humans to mitigate disuse- and age-related skeletal muscle loss, it is imperative that we evaluate critical regulators of skeletal muscle atrophy from a system to the cellular level. The symposium "Regulation of Muscle Atrophy: Wasting Away from the Outside In" was presented at the ACSM Annual Meeting in Indianapolis on May 29, 2008, to provide an overview of the skeletal muscle atrophy literature and our current understanding of the atrophy program from the whole system to the molecular level. In addition, this symposium addressed the feasibility of intervening with specific countermeasures to attenuate atrophy. This introduction identifies the scope of the symposium, which evaluates our current understanding of the atrophy program and how this information can facilitate the development of effective countermeasures.
Insights
Skeletal muscle loss during detraining, disuse, injury, and aging involves unique molecular changes. Developing effective countermeasures requires understanding regulators of muscle atrophy from system to cellular levels.
Area of Science:
- Muscle physiology and molecular biology.
- Cellular and systemic regulation of skeletal muscle mass.
Background:
- Periods of detraining, disuse, injury, and aging lead to skeletal muscle mass and function loss.
- Unique molecular signaling alterations occur depending on the perturbation causing muscle loss.
- Current interventions effectively promote muscle hypertrophy but not attenuate atrophy.
Purpose of the Study:
- To provide an overview of skeletal muscle atrophy literature.
- To elucidate the molecular mechanisms underlying muscle loss.
- To evaluate critical regulators of skeletal muscle atrophy and potential countermeasures.
Main Methods:
- Review of emerging literature on skeletal muscle atrophy.
- Discussion of phenotypic adaptations and regulatory factors.
- Evaluation of gene therapy, pharmacological, and nutritional interventions.
Main Results:
- Specific molecular signaling alterations are linked to different causes of muscle loss.
- Effective methods exist for promoting muscle hypertrophy.
- Attenuating skeletal muscle atrophy remains a challenge.
Conclusions:
- Understanding muscle atrophy at molecular and systemic levels is crucial.
- Developing effective countermeasures for disuse- and age-related muscle loss is imperative.
- Further research into critical regulators can facilitate intervention strategies.
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