Neuromuscular electrical stimulation prevents muscle disuse atrophy during leg immobilization in humans

被引:191
作者
Dirks, M. L. [1 ]
Wall, B. T. [1 ]
Snijders, T. [1 ]
Ottenbros, C. L. P. [2 ]
Verdijk, L. B. [1 ]
van Loon, L. J. C. [1 ]
机构
[1] Maastricht Univ, NUTRIM Sch Nutr Toxicol & Metab, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Med Ctr, Dept Surg, NL-6200 MD Maastricht, Netherlands
关键词
disuse atrophy; immobilization; neuromuscular electrical stimulation; skeletal muscle; HUMAN SKELETAL-MUSCLE; CHRONIC HEART-FAILURE; HUMAN QUADRICEPS MUSCLE; BED-REST; PROTEIN-SYNTHESIS; RESISTANCE EXERCISE; SATELLITE CELL; OLDER-ADULTS; ANABOLIC RESISTANCE; NEGATIVE REGULATOR;
D O I
10.1111/apha.12200
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
AimShort periods of muscle disuse, due to illness or injury, result in substantial skeletal muscle atrophy. Recently, we have shown that a single session of neuromuscular electrical stimulation (NMES) increases muscle protein synthesis rates. The aim was to investigate the capacity for daily NMES to attenuate muscle atrophy during short-term muscle disuse. MethodsTwenty-four healthy, young (231year) males participated in the present study. Volunteers were subjected to 5days of one-legged knee immobilization with (NMES; n=12) or without (CON; n=12) supervised NMES sessions (40-min sessions, twice daily). Two days prior to and immediately after the immobilization period, CT scans and single-leg one-repetition maximum (1RM) strength tests were performed to assess quadriceps muscle cross-sectional area (CSA) and leg muscle strength respectively. Furthermore, muscle biopsies were taken to assess muscle fibre CSA, satellite cell content and mRNA and protein expression of selected genes. ResultsIn CON, immobilization reduced quadriceps CSA by 3.5 +/- 0.5% (P<0.0001) and muscle strength by 9 +/- 2% (P<0.05). In contrast, no significant muscle loss was detected following immobilization in NMES although strength declined by 7 +/- 3% (P<0.05). Muscle MAFbx and MuRF1 mRNA expression increased following immobilization in CON (P<0.001 and P=0.07 respectively), whereas levels either declined (P<0.01) or did not change in NMES, respectively. Immobilization led to an increase in muscle myostatin mRNA expression in CON (P<0.05), but remained unchanged in NMES. ConclusionDuring short-term disuse, NMES represents an effective interventional strategy to prevent the loss of muscle mass, but it does not allow preservation of muscle strength. NMES during disuse may be of important clinical relevance in both health and disease.
引用
收藏
页码:628 / 641
页数:14
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