Regulation of Neurotrophin-3 and Interleukin-1β and Inhibition of Spinal Glial Activation Contribute to the Analgesic Effect of Electroacupuncture in Chronic Neuropathic Pain States of Rats

被引:12
|
作者
Tu, Wenzhan [1 ,2 ]
Wang, Wansheng [3 ]
Xi, Haiyan [4 ]
He, Rong [1 ,2 ]
Gao, Liping [1 ,2 ]
Jiang, Songhe [1 ,2 ]
机构
[1] Wenzhou Med Univ, Dept Phys Med & Rehabil, Affiliated Hosp 2, Wenzhou 325027, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Zhejiang, Peoples R China
[3] Binzhou Med Univ, Affiliated Hosp, Dept Rehabil Med, Binzhou 256603, Shandong, Peoples R China
[4] Binzhou Med Univ, Affiliated Hosp, Dept Gynecol, Binzhou 256603, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
LONG-TERM POTENTIATION; CHRONIC CONSTRICTION; THERMAL HYPERALGESIA; LAMINA I; RECEPTOR; EXPRESSION; MICROGLIA; NEURONS; INJURY; INVOLVEMENT;
D O I
10.1155/2015/642081
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Growing evidence indicates that neurotrophin-3, interleukin-1 beta, and spinal glia are involved in neuropathic pain derived from dorsal root ganglia to spinal cord. Electroacupuncture is widely accepted to treat chronic pain, but the precise mechanism underlying the analgesic effect of EA has not been fully demonstrated. In this study, the mechanical withdrawal threshold and thermal withdrawal latency were recorded. We used immunofluorescence and western blots methods to investigate the effect of EA on the expression of NT-3 and IL-1 beta in DRG and spinal cord of CCI rats; we also examined the expression of spinal GFAP and OX-42 in spinal cord. In present study, the MWT and TWL of CCI group rats were lower than those in the Sham CCI group rats, but EA treatment increased the pain thresholds. Furtherly, we found that EA upregulates the expression of NT-3 in DRG and spinal cord of CCI rats, while EA downregulates the expression of IL-1 beta. Additionally, immunofluorescence exhibited that CCI-induced activation of microglia and astrocytes was inhibited significantly by EA treatment. These results demonstrated that the analgesic effect of EA may be achieved through promoting the neural protection of NT-3 as well as the inhibition of IL-1 beta production and spinal glial activity.
引用
收藏
页数:9
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