Involvement of spinal orexin A in the electroacupuncture analgesia in a rat model of post-laparotomy pain
Involvement of spinal orexin A in the electroacupuncture analgesia in a rat model of post-laparotomy pain
复制标题
脊髓食欲素A参与电针镇痛大鼠剖腹术后疼痛模型
DOI:
10.1186/1472-6882-12-225
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发表时间:
2012-11-22
影响因子:
--
通讯作者:
Wu, Gen-Cheng
中科院分区:
文献类型:
--
作者:
Feng, Xiao-Ming;Mi, Wen-Li;Wu, Gen-Cheng
BackgroundOrexin A (OXA, hypocretin/hcrt 1) is a newly discovered potential analgesic substance. However, whether OXA is involved in acupuncture analgesia remains unknown. The present study was designed to investigate the involvement of spinal OXA in electroacupuncture (EA) analgesia.MethodsA modified rat model of post-laparotomy pain was adopted and evaluated. Von Frey filaments were used to measure mechanical allodynia of the hind paw and abdomen. EA at 2/15 Hz or 2/100 Hz was performed once on the bilateral ST36 and SP6 for 30 min perioperatively. SB-334867, a selective orexin 1 receptor (OX1R) antagonist with a higher affinity for OXA than OXB, was intrathecally injected to observe its effect on EA analgesia.ResultsOXA at 0.3 nmol and EA at 2/15 Hz produced respective analgesic effects on the model (P<0.05). Pre-surgical intrathecal administered of SB-334867 30 nmol antagonized OXA analgesia and attenuated the analgesic effect of EA (P<0.05). However, SB-334867 did not block fentanyl-induced analgesia (P>0.05). In addition, naloxone, a selective opioid receptor antagonist, failed to antagonize OXA-induced analgesia (P>0.05).ConclusionsThe results of the present study indicate the involvement of OXA in EA analgesia via OX1R in an opioid-independent way.