Acupuncture plus low-frequency electrical stimulation (Acu-LFES) attenuates denervation-induced muscle atrophy

J Appl Physiol (1985). 2016 Feb 15;120(4):426-36. doi: 10.1152/japplphysiol.00175.2015. Epub 2015 Dec 17.

Abstract

Muscle wasting occurs in a variety of clinical situations, including denervation. There is no effective pharmacological treatment for muscle wasting. In this study, we used a tibial nerve denervation model to test acupuncture plus low-frequency electric stimulation (Acu-LFES) as a therapeutic strategy for muscle atrophy. Acupuncture needles were connected to an SDZ-II electronic acupuncture device delivering pulses at 20 Hz and 1 mA; the treatment was 15 min daily for 2 wk. Acu-LFES prevented soleus and plantaris muscle weight loss and increased muscle cross-sectional area in denervated mice. The abundances of Pax7, MyoD, myogenin, and embryonic myosin heavy chain were significantly increased by Acu-LFES in both normal and denervated muscle. The number of central nuclei was increased in Acu-LFES-treated muscle fibers. Phosphorylation of Akt was downregulated by denervation leading to a decline in muscle mass; however, Acu-LFES prevented the denervation-induced decline largely by upregulation of the IGF-1 signaling pathway. Acu-LFES reduced the abundance of muscle catabolic proteins forkhead O transcription factor and myostatin, contributing to the attenuated muscle atrophy. Acu-LFES stimulated the expression of macrophage markers (F4/80, IL-1b, and arginase-1) and inflammatory cytokines (IL-6, IFNγ, and TNFα) in normal and denervated muscle. Acu-LFES also stimulated production of the muscle-specific microRNAs miR-1 and miR-206. We conclude that Acu-LFES is effective in counteracting denervation-induced skeletal muscle atrophy and increasing muscle regeneration. Upregulation of IGF-1, downregulation of myostatin, and alteration of microRNAs contribute to the attenuation of muscle atrophy in denervated mice.

Keywords: Akt; FoxO; IGF-1; cytokines; macrophage; myostatin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acupuncture Therapy / methods*
  • Animals
  • Cytokines / metabolism
  • Down-Regulation / physiology
  • Electric Stimulation / methods*
  • Forkhead Transcription Factors / metabolism
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / metabolism
  • Muscle Denervation / adverse effects*
  • Muscle Fibers, Skeletal / metabolism*
  • Muscle Proteins / metabolism
  • Muscular Atrophy / metabolism
  • Muscular Atrophy / therapy*
  • Myosin Heavy Chains / metabolism
  • Myostatin / metabolism
  • Needles
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / physiology
  • Tibial Nerve / metabolism
  • Up-Regulation / physiology

Substances

  • Cytokines
  • Forkhead Transcription Factors
  • MicroRNAs
  • Muscle Proteins
  • Myostatin
  • Insulin-Like Growth Factor I
  • Proto-Oncogene Proteins c-akt
  • Myosin Heavy Chains