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Acta Physiologica 2008; Volume 194, Supplement 665
The 59th National Congress of the Italian Physiological Society
9/17/2008-9/19/2008
Cagliari, Italy
DIFFERENT TRAININGS INDUCED SPECIFIC CELLULAR AND MOLECULAR MODIFICATIONS IN AGED HUMAN SKELETAL MUSCLE
Abstract number: P109
PIETRANGELO1 T, TONIOLO2 L, REGGIANI2 C, FANO'1 G, FULLE1 S
1Dept. Basic and Applied Medical Science, Interuniversity Institute of Myology, University G. dAnnunzio, Chieti
2Dept. Human Anatomy and Physiology, University of [email protected]
Aim:
Sarcopenia means the physiological reduction of skeletal muscle mass and strength in elderly individuals (Fulle et al, 2005). The purpose of our study was to study the effects of different trainings (endurance, resistance and local vibrational energy) in elderly.
Methods:
We enrolled healthy 6585 y-old subjects and randomly assigned them to a specific training of 12 weeks. Before and after the training, we made a biopsy of vastus lateralis and divided it in three fragments for: (i) the specific tension development of single fibers and the expression of myosin heavy chain proteins; (ii) the transcriptional profile and (iii) the regenerative capacity of satellite cells.
Results:
The single fiber strength development does not change with any training protocol. Considering the gene expression profiles, each physical activity share a stimulation of a specific metabolic pathway; both endurance and vibrational training up regulate genes involved in aerobic metabolism while the resistance training stimulates that of creatine pathway. All training, with different modalities, stimulate the expression of some sarcomeric and/or cytoskeletal proteins. In particular vibrational training stimulates proteins linked to Z-line while endurance induces the over expression of protein for neuronal chemotaxis.
Conclusion:
In conclusion, our results suggest that all training performed counteract Sarcopenia progression and each of them are able to stimulate specific molecular signalling which, in turn effects specific metabolic pathways.
To cite this abstract, please use the following information:
Acta Physiologica 2008; Volume 194, Supplement 665 :P109