The muscle protein synthetic response to the combined ingestion of protein and carbohydrate is not impaired in healthy older men
Aging is associated with a progressive decline in skeletal muscle mass. It has been hypothesized that an attenuated muscle protein synthetic response to the main anabolic stimuli may contribute to the age-related loss of muscle tissue. The aim of the present study was to compare the muscle protein s...
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Veröffentlicht in: | AGE 2013-12, Vol.35 (6), p.2389-2398 |
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Sprache: | eng |
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Zusammenfassung: | Aging is associated with a progressive decline in skeletal muscle mass. It has been hypothesized that an attenuated muscle protein synthetic response to the main anabolic stimuli may contribute to the age-related loss of muscle tissue. The aim of the present study was to compare the muscle protein synthetic response following ingestion of a meal-like amount of dietary protein plus carbohydrate between healthy young and older men. Twelve young (21 ± 1 years) and 12 older (75 ± 1 years) men consumed 20 g of intrinsically
l
-[1-
13
C]phenylalanine-labeled protein with 40 g of carbohydrate. Ingestion of specifically produced intrinsically
l
-[1-
13
C]phenylalanine-labeled protein allowed us to assess the subsequent incorporation of casein-derived amino acids into muscle protein. Blood samples were collected at regular intervals, with muscle biopsies obtained prior to and 2 and 6 h after protein plus carbohydrate ingestion. The acute post-prandial rise in plasma glucose and insulin concentrations was significantly greater in the older compared with the younger males. Plasma amino acid concentrations increased rapidly following drink ingestion in both groups. However, plasma leucine concentrations were significantly lower at
t
= 90 min in the older when compared with the young group (
P
0.05). We conclude that the use of dietary protein-derived amino acids for muscle protein synthesis is not impaired in healthy older men following intake of protein plus carbohydrate. |
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ISSN: | 0161-9152 2509-2715 1574-4647 2509-2723 |
DOI: | 10.1007/s11357-013-9522-2 |