Electroacupuncture exerts an anti-migraine effect via modulation of the 5-HT7 receptor in the conscious rat

电针 医学 中缝大核 针灸科 刺激 偏头痛 麻醉 方差分析 痛觉超敏 内科学 内分泌学 受体 痛觉过敏 5-羟色胺能 伤害 血清素 病理 替代医学
作者
Pei Pei,Lu Liu,Luopeng Zhao,Zhengyang Qu,Chu-ying Tang,Linpeng Wang,Wenming Yang
出处
期刊:Acupuncture in Medicine [SAGE Publishing]
卷期号:37 (1): 47-54 被引量:25
标识
DOI:10.1136/acupmed-2017-011410
摘要

Acupuncture has been recommended as an alternative therapy for migraine. Emerging evidence suggests that the 5-HT7 receptor (5-HT7R) plays a significant facilitatory role in descending modulation in migraine pathophysiology, and that activation of 5-HT7R in the descending pathway is involved in migraine central sensitisation.To investigate the ability of electroacupuncture (EA) to ameliorate central sensitisation via modulation of 5-HT7R in the descending pain pathways using a rat model of migraine induced by repetitive dural electrical stimulation (DES).64 male Sprague-Dawley rats were randomly divided into four groups: Normal group; DES group (receiving dural electrical stimulation only); DES+GB20 group (DES model group treated with EA at GB20); and DES+Sham group (DES model group treated with EA at a non-traditional (sham) acupuncture point). The presence of cutaneous allodynia was determined by measuring facial and hind-paw withdrawal latencies to electronic von-Frey. The expression of 5-HT7R in the descending pathways (periaqueductal grey, raphe magnus nucleus, and trigeminal nucleus caudalis) was assessed using immunofluorescence and Western blotting.Facial and hind-paw withdrawal thresholds were significantly increased in the DES+GB20 group compared with the untreated DES group. The expression of 5-HT7R was significantly decreased in the DES+GB20 group compared with the DES group (one-way analysis of variance (ANOVA), P<0.05). No significant differences in behaviour or expression were found between the rats in the DES+Sham group and the untreated DES group (one-way ANOVA, P>0.05).EA at GB20 may ameliorate central sensitisation in migraine by inhibiting the activation of 5-HT7 receptors in the descending pain pathway in a rat model of migraine.
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