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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:
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.
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页码:364 / 374
页数:11
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