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

被引:0
|
作者
Hong, En-si [1 ]
Yao, Hai-hua [2 ]
Min, You-jiang [1 ,2 ]
Sun, Jie [1 ]
Zhou, Xuan [1 ]
Zeng, Xue-bo [1 ]
Yu, Wan [1 ]
机构
[1] Jiangxi Univ Tradit Chinese Med, Affiliated Hosp, Nanchang 330006, Jiangxi, Peoples R China
[2] Shanghai Eighth Peoples Hosp, Shanghai 200235, Peoples R China
来源
JOURNAL OF SPINAL CORD MEDICINE | 2021年 / 44卷 / 03期
基金
中国国家自然科学基金;
关键词
RhoA; ROCKII; SCI; MLC; cPLA2; PGE(2); Y27632; Electroacupuncture; RHO-ASSOCIATED KINASE; PHOSPHOLIPASE A(2); OUTGROWTH; PROTEIN;
D O I
10.1080/10790268.2019.1665612
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 PGE(2) 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.
引用
收藏
页码:364 / 374
页数:11
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