High levels of physical activity in later life are associated with enhanced markers of mitochondrial metabolism
The age-associated reduction in muscle mass is well characterised, however less is known regarding the mechanisms responsible for the decline in oxidative capacity also observed with advancing age. The purpose of the current study was therefore to compare mitochondrial gene expression and protein content between young and old recreationally active, and older highly active individuals. Muscle biopsies were obtained from the vastus lateralis of young males (YG: 22+/-3 years) and older (OG: 67+/-2 years) males not previously engaged in formal exercise and older male master cyclists (OT: 65+/-5 years) who had undertaken cycling exercise for 32+/-17 yrs. Comparison of gene expression between YG, OG and OT groups revealed greater expression of mitochondrial-related genes, namely electron transport chain (ETC) complexes II, III, IV (p<.05) in OT compared to YG and OG. Gene expression of mitofusion (MFN)-1/2, mitochondrial fusion genes, were greater in OT compared to OG (p<.05). Similarly, protein content of ETC complexes I, II and IV were significantly greater in OT compared to both YG and OG (p<.001). Protein content of peroxisome proliferator-activated receptor gamma, coactivator 1 alpha (PGC-1alpha), was greater in OT compared to YG and OG (p<.001). Our results suggest that the aging process per se, is not associated with a decline in gene expression and protein content of ETC complexes. Mitochondrial-related gene expression and protein content is substantially greater in OT, suggesting that exercise-mediated increases in mitochondrial content can be maintained into later life.
|ISBN||1758-535X (Electronic) 1079-5006 (Linking)|
|Authors||Joanisse, S.; Ashcroft, S.; Wilkinson, D. J.; Pollock, R. D.; O'Brien, K. A.; Phillips, B. E.; Smith, K.; Lazarus, N. R.; Harridge, S.; Atherton, P. J.; Philp, A.|
|Responsible Garvan Author||Dr Andy Philp|
|Publisher Name||JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES|
|URL link to publisher's version||https://www.ncbi.nlm.nih.gov/pubmed/31942994|