Low-intensity microcurrent therapy promotes regeneration of atrophied calf muscles in immobilized rabbits

Gi Young Park, Dong Rak Kwon, Yong Suk Moon

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Journal of Biomedical Research ›› 2019, Vol. 33 ›› Issue (1) : 30-37. DOI: 10.7555/JBR.32.20180056
Original Article
Original Article

Low-intensity microcurrent therapy promotes regeneration of atrophied calf muscles in immobilized rabbits

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Abstract

The purpose of this study was to investigate the intensity-specific regenerative effects of microcurrent therapy on gastrocnemius muscle atrophy induced by cast-immobilization in rabbits. Fifteen rabbits were randomly allocated to 3 groups after cast removal: cast-immobilization and sham microcurrent therapy for 2 weeks (group 1); cast-immobilization and microcurrent therapy (25 mA) for 2 weeks (group 2); cast-immobilization and microcurrent therapy (5,000 mA) for 2 weeks (group 3). Clinical parameters [calf circumference, compound muscle action potential (CMAP) of the tibial nerve, thickness of gastrocnemius muscle], cross sectional area of gastrocnemius muscle fibres, and immunohistochemistry was evaluated. The clinical parameters representing mean atrophic changes in group 2 were significantly lower than those in group 3. The cross sectional area of the gastrocnemius muscle fibres and immunohistochemical parameters in group 2 were significantly greater than those in group 3. The results showed that low-intensity microcurrent therapy can more effectively promote regeneration in atrophied gastrocnemius muscle than high-intensity microcurrent therapy.

Keywords

microcurrent / intensity / atrophy / muscle / cast

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Gi Young Park, Dong Rak Kwon, Yong Suk Moon. Low-intensity microcurrent therapy promotes regeneration of atrophied calf muscles in immobilized rabbits. Journal of Biomedical Research, 2019, 33(1): 30‒37 https://doi.org/10.7555/JBR.32.20180056

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Acknowledgment

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) and funded by the Ministry of Education (NRF-2016R1D1A1B01014260).

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2018 2018 by the Journal of Biomedical Research.
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