论文部分内容阅读
本实验利用大鼠甩尾测痛结合脊髓蛛网膜下腔注药的方法,观察了脊髓水平内源性阿片样物质(OLS)对5一羟色胺(5—HT)4痛作用的影响。实验结果显示;(1)脊髓蛛网膜下腔注射60nmol的5—HT可产生明显的镇痛作用,并可为同一途径注射阿片受体阻断剂纳络酮所完全阻断;(2)同一剂量的纳络酮也能阻断鞘内注射60nmol吗啡所引起的镇痛作用;(3)单独使用120nmol纳络酮对痛阈无明显影响。以上结果表明.在脊髓水平5—HL的镇痛作用是通过OLS介导的。
In this study, we investigated the effect of endogenous spinal opioid (OLS) on 5-hydroxytryptamine (5-HT) 4 pain by using the method of tail flicking and painful spinal subarachnoid injection in rats. The experimental results showed that: (1) Spinal subarachnoid injection of 60nmol of 5-HT can produce significant analgesic effect, and can be completely blocked by the same route of injection of opioid receptor blocker naloxone; (2) the same The dose of naloxone also blocked intrathecal injection of 60nmol morphine induced analgesic effect; (3) 120nmol naloxone alone had no significant effect on the pain threshold. The above result shows. The analgesic effect of 5-HL at spinal level is mediated by OLS.