Tian J H, Xu W, Zhang W, Fang Y, Grisel J E, Mogil J S, Grandy D K, Han J S
Neuroscience Research Center, Beijing Medical University, PR China.
Neuroreport. 1997 Jan 20;8(2):497-500. doi: 10.1097/00001756-199701200-00024.
Recent studies suggest that the novel opioid peptide orphanin FQ (OFQ) is involved in pain modulation. We found that intracerebroventricular (i.c.v.) administration of OFQ in the rat produced a dose-dependent antagonism of the analgesia induced by 100 Hz electroacupuncture (EA) stimulation as measured in the radiant heat tail-flick assay. Antisense oligonucleotides injected i.c.v. potentiated EA analgesia, presumably by interfering with the expression of the OFQ receptor in brain. These results suggest that endogenous OFQ exerts a tonic antagonistic effect on EA-induced analgesia. No such antagonism was observed when OFQ was injected intrathecally (i.t.). Rather, it appears that spinal OFQ produced a marked analgesic effect and enhanced EA-induced analgesia. These findings are consistent with the experimental results obtained in rats where morphine-induced analgesia is antagonized by i.c.v. OFQ and potentiated by i.t. OFQ.
最近的研究表明,新型阿片样肽孤啡肽(OFQ)参与疼痛调节。我们发现,在大鼠脑室内(i.c.v.)注射OFQ,在辐射热甩尾试验中可产生剂量依赖性地拮抗100Hz电针(EA)刺激诱导的镇痛作用。脑室内注射反义寡核苷酸可增强EA镇痛作用,推测是通过干扰脑中OFQ受体的表达。这些结果表明,内源性OFQ对EA诱导的镇痛作用具有紧张性拮抗作用。当鞘内(i.t.)注射OFQ时未观察到这种拮抗作用。相反,脊髓OFQ似乎产生了显著的镇痛作用并增强了EA诱导的镇痛作用。这些发现与在大鼠中获得的实验结果一致,在大鼠中,脑室内注射OFQ可拮抗吗啡诱导的镇痛作用,而鞘内注射OFQ可增强该作用。