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Exp Gerontol. 2012 Jun;47(6):417-24. doi: 10.1016/j.exger.2012.03.004. Epub 2012 Mar 17.

The effects of aging, physical training, and a single bout of exercise on mitochondrial protein expression in human skeletal muscle.

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1
Research Institute of Sport Science, Semmelweis University, Budapest, Hungary.

Abstract

Aging results in a significant decline in aerobic capacity and impaired mitochondrial function. We have tested the effects of moderate physical activity on aerobic capacity and a single bout of exercise on the expression profile of mitochondrial biogenesis, and fusion and fission related genes in skeletal muscle of human subjects. Physical activity attenuated the aging-associated decline in VO2 max (p<0.05). Aging increased and a single exercise bout decreased the expression of nuclear respiratory factor-1 (NRF1), while the transcription factor A (TFAM) expression showed a strong relationship with VO(2max) and increased significantly in the young physically active group. Mitochondrial fission representing FIS1 was induced by regular physical activity, while a bout of exercise decreased fusion-associated gene expression. The expression of polynucleotide phosphorylase (PNPase) changed inversely in young and old groups and decreased with aging. The A2 subunit of cyclic AMP-activated protein kinase (AMPK) was induced by a single bout of exercise in skeletal muscle samples of both young and old subjects (p<0.05). Our data suggest that moderate levels of regular physical activity increases a larger number of mitochondrial biogenesis-related gene expressions in young individuals than in aged subjects. Mitochondrial fission is impaired by aging and could be one of the most sensitive markers of the age-associated decline in the adaptive response to physical activity.

PMID:
22449457
PMCID:
PMC4915826
DOI:
10.1016/j.exger.2012.03.004
[Indexed for MEDLINE]
Free PMC Article
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