Transcutaneous neuromuscular electrical stimulation effect on the degree of microvascular perfusion in autonomically denervated rat skeletal muscle

1996 ◽  
Vol 77 (2) ◽  
pp. 155-160 ◽  
Author(s):  
F.Richard Clemente ◽  
Kirk W. Barron
2010 ◽  
Vol 12 (10) ◽  
pp. 900-908 ◽  
Author(s):  
E. A. Bradley ◽  
K. J. Willson ◽  
D. Choi-Lundberg ◽  
M. G. Clark ◽  
S. Rattigan

2021 ◽  
Vol 9 (9) ◽  
Author(s):  
Takaya Kotani ◽  
Junya Takegaki ◽  
Yuki Tamura ◽  
Karina Kouzaki ◽  
Koichi Nakazato ◽  
...  

2011 ◽  
Vol 110 (2) ◽  
pp. 433-450 ◽  
Author(s):  
Julien Gondin ◽  
Lorenza Brocca ◽  
Elena Bellinzona ◽  
Giuseppe D'Antona ◽  
Nicola A. Maffiuletti ◽  
...  

The aim of the present study was to define the chronic effects of neuromuscular electrical stimulation (NMES) on the neuromuscular properties of human skeletal muscle. Eight young healthy male subjects were subjected to 25 sessions of isometric NMES of the quadriceps muscle over an 8-wk period. Needle biopsies were taken from the vastus lateralis muscle before and after training. The training status, myosin heavy chain (MHC) isoform distribution, and global protein pattern, as assessed by proteomic analysis, widely varied among subjects at baseline and prompted the identification of two subgroups: an “active” (ACT) group, which performed regular exercise and had a slower MHC profile, and a sedentary (SED) group, which did not perform any exercise and had a faster MHC profile. Maximum voluntary force and neural activation significantly increased after NMES in both groups (+∼30% and +∼10%, respectively). Both type 1 and 2 fibers showed significant muscle hypertrophy. After NMES, both groups showed a significant shift from MHC-2X toward MHC-2A and MHC-1, i.e., a fast-to-slow transition. Proteomic maps showing ∼500 spots were obtained before and after training in both groups. Differentially expressed proteins were identified and grouped into functional categories. The most relevant changes regarded 1) myofibrillar proteins, whose changes were consistent with a fast-to-slow phenotype shift and with a strengthening of the cytoskeleton; 2) energy production systems, whose changes indicated a glycolytic-to-oxidative shift in the metabolic profile; and 3) antioxidant defense systems, whose changes indicated an enhancement of intracellular defenses against reactive oxygen species. The adaptations in the protein pattern of the ACT and SED groups were different but were, in both groups, typical of both resistance (i.e., strength gains and hypertrophy) and endurance (i.e., a fast-to-slow shift in MHC and metabolic profile) training. These training-induced adaptations can be ascribed to the peculiar motor unit recruitment pattern associated with NMES.


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