Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/35151
Title: Optimizing electrical stimulation for promoting satellite cell proliferation in muscle disuse atrophy
Authors: Wan, Q
Yeung, S 
Cheung, KK 
Au, SW
Lam, WW
Li, YH
Dai, ZQ
Yeung, EW 
Keywords: Muscle atrophy
Electrical stimulation
Satellite cells
Hindlimb suspension
Issue Date: Jan-2016
Publisher: Lippincott Williams & Wilkins
Source: American journal of physical medicine and rehabilitation, Jan. 2016, v. 95, no. 1, p. 28-38 How to cite?
Journal: American journal of physical medicine and rehabilitation 
Abstract: Objective: The aim of this study was to investigate the optimal electrical stimulation (ES) protocol in attenuating disuse muscle atrophy by influencing satellite cell activity.
Design: This study used a pretest-posttest design. Six ES protocols of different duration (3 hrs day⁻¹ or 2 × 3 hrs day⁻¹) and frequencies (2, 10, or 20 Hz) were applied on the soleus muscle in mice (n = 8 in each group) that were hindlimb-suspended for 14 days. Muscle mass, cross-sectional area and fiber-type composition, and peak tetanic force of the muscles were measured. Immunohistochemical staining was used to evaluate satellite cell content, activation, proliferation, and differentiation. Cell apoptosis was detected by TdT-mediated dUTP nick end labeling (TUNEL) assay.
Results: ES at 2 Hz for 2 × 3 hrs day⁻¹ achieved the best effect in attenuating the loss of muscle fiber cross-sectional area and force. This stimulation parameter led to a 1.2-fold increase in satellite cell proliferation and was effective in rescuing cells from apoptosis. Besides, satellite cells in the atrophic muscles required different stimulation protocols for different cellular activities such as activation, proliferation, and myogenic differentiation.
Conclusions: This study showed that ES at 2 Hz for 2 × 3 hrs day⁻¹ is the optimal protocol for counteracting muscle disuse atrophy.
URI: http://hdl.handle.net/10397/35151
ISSN: 0894-9115
DOI: 10.1097/PHM.0000000000000307
Rights: Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved.
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