The mechanism of electroacupuncture for treating spinal cord injury rats by mediating Rho/Rho-associated kinase signaling pathway

J Spinal Cord Med. 2021 May;44(3):364-374. doi: 10.1080/10790268.2019.1665612. Epub 2019 Oct 9.

Abstract

Objective: To determine the changes of gene and protein expression through Rho/ROCK signaling pathway in EA treated spinal cord injury (SCI) rats and to unveil the possible underlying mechanism.Design: Animal study.Setting: Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine.Participants: Eighty Male Sprague Dawley rats.Interventions: Electroacupuncture at Yaoyangguan (GV3), Dazhui (GV14), Zusanli (ST36) and Ciliao (BL32) and/or blocking agent Y27632 treatment.Outcome Measures: Protein expression was detected by ELISA and Western blotting, mRNA expression was detected by quantitative PCR and in situ hybridization. Morphological changes in spinal cord were evaluated by HE-staining and Nissl staining. Hindlimb motor function in the rats was evaluated by Basso-Beattie-Bresnahan (BBB) assessment methods.Results: Compared with injured rats in SCI group, EA, blocking agent Y27632 and EA + blocking agent Y27632 treatment had significantly reduced mRNA and protein expression levels of RhoA and ROCKII, decreased p-MLC protein expression and p-MLC/MLC ratio, suppressed cPLA2 activity and PGE2 level, improved spinal cord tissue morphology and BBB score of lower limb movement function at 7 days and at 14 days (P < 0.01 or <0.05).Conclusion: Similar to the blocking agent Y27632, EA may have a notable inhibitory effect on the Rho/ROCK signaling pathway after SCI, therefore reducing the inhibition of axonal growth and inflammatory reaction may be a key mechanism of EA treatment for SCI.

Keywords: Electroacupuncture; MLC; PGE2; ROCKII; RhoA; SCI; Y27632; cPLA2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Electroacupuncture*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction*
  • Spinal Cord
  • Spinal Cord Injuries* / therapy
  • rho GTP-Binding Proteins / metabolism*
  • rho-Associated Kinases / metabolism*

Substances

  • rho-Associated Kinases
  • rho GTP-Binding Proteins

Grants and funding

This work was supported by the National Natural Science Foundation of China (CN) (No. 81360562, 81904289).