» Articles » PMID: 8498491

Myofibrillar Protein Synthesis in Young and Old Men

Overview
Journal Am J Physiol
Specialty Physiology
Date 1993 May 1
PMID 8498491
Citations 70
Authors
Affiliations
Soon will be listed here.
Abstract

We tested the hypothesis that healthy older men (> 60 yr old) have a slower rate of myofibrillar protein synthesis than young men (< 35 yr old). Myofibrillar protein synthesis was determined by the in vivo incorporation of L-[1-13C]leucine into myofibrillar proteins obtained by muscle biopsy. Subjects were eight young (21-31 yr) and eight older (62-81 yr) men, all healthy and moderately active. There was no significant difference in the mean height and weight of the two age groups, but the older group had 12% less lean body mass (determined by 40K counting) and 21% less muscle mass (estimated by urinary creatinine excretion). Upper leg strength was approximately one-third lower in the older subjects according to isokinetic dynamometry. The fractional rate of myofibrillar protein synthesis was 28% slower in the older group (0.039 +/- 0.009 vs. 0.054 +/- 0.010 %/h, mean +/- SD, P < 0.01). Total myofibrillar protein synthesis, estimated as total myofibrillar mass (from creatinine excretion) times the fractional synthesis rate, was 44% slower in the older group (1.4 vs. 2.5 g/h, P < 0.001). Whole body protein synthesis, assessed as the difference between leucine disappearance rate and leucine oxidation, was marginally slower (8%, P = 0.10) in the older group, but not when the data were adjusted for lean body mass. Myofibrillar protein synthesis was a smaller fraction of whole body protein synthesis in the older group (12 vs. 19%). Reduced myofibrillar protein synthesis may be an important mechanism of the muscle atrophy associated with aging.

Citing Articles

The Role of Branched Chain Ketoacid Dehydrogenase Kinase (BCKDK) in Skeletal Muscle Biology and Pathogenesis.

Fernicola J, Vyavahare S, Gupta S, Kalwaghe A, Kosmac K, Davis A Int J Mol Sci. 2024; 25(14).

PMID: 39062842 PMC: 11277350. DOI: 10.3390/ijms25147601.


Sexual dimorphisms in skeletal muscle: current concepts and research horizons.

Emmert M, Emmert A, Goh Q, Cornwall R J Appl Physiol (1985). 2024; 137(2):274-299.

PMID: 38779763 PMC: 11343095. DOI: 10.1152/japplphysiol.00529.2023.


Anabolic Resistance in the Pathogenesis of Sarcopenia in the Elderly: Role of Nutrition and Exercise in Young and Old People.

Tezze C, Sandri M, Tessari P Nutrients. 2023; 15(18).

PMID: 37764858 PMC: 10535169. DOI: 10.3390/nu15184073.


Evidence for inefficient contraction and abnormal mitochondrial activity in sarcopenia using magnetic resonance spectroscopy.

Stephenson M, Ho J, Migliavacca E, Kalimeri M, Karnani N, Banerji S J Cachexia Sarcopenia Muscle. 2023; 14(3):1482-1494.

PMID: 37143433 PMC: 10235891. DOI: 10.1002/jcsm.13220.


The contributory role of vascular health in age-related anabolic resistance.

Banks N, Rogers E, Church D, Ferrando A, Jenkins N J Cachexia Sarcopenia Muscle. 2021; 13(1):114-127.

PMID: 34951146 PMC: 8818606. DOI: 10.1002/jcsm.12898.