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• 基础研究 • 上一篇    下一篇

青龙木叶皂苷的镇痛作用及其机制

王丽华1,马颖哲1,杨成军1,张桂荣1*,唐玉环1,王 绍2,郭 超3   

  1. 1. 吉林大学基础医学院生物化学和分子生物学教研室,吉林 长春130021;2. 吉林大学基础医学院生理学教研室,吉林 长春130021;3.长春精优药业股份有限公司,吉林 长春130033
  • 收稿日期:2005-03-09 修回日期:1900-01-01 出版日期:2005-11-28 发布日期:2005-11-28
  • 通讯作者: 张桂荣

Analgesic action of total saponin of Pterocarpus Indicus and its mechanism

WANG Li-hua1,MA Ying-zhe1,YANG Cheng-jun1,ZHANG Gui-rong1*,TANG Yu-huan1,WANG Shao2,GUO Chao3   

  1. 1. Department of Biochemistry and Molecular Biology,School of Basic Medical Sciences,Jilin University,Changchun 130021,China;2.Department of Physiology, School of Medical Sciences,Jilin University,Changchun 130021,China;3.Changchun Extrawell Pharmaceutical Co.,Ltd, Changchun 130033,China
  • Received:2005-03-09 Revised:1900-01-01 Online:2005-11-28 Published:2005-11-28
  • Contact: ZHANG Gui-rong

摘要: 目的:探讨青龙木叶皂苷的镇痛效应及其机制。 方法:60只Wistar大鼠随机分为5组(每组12只):青龙木叶皂苷15、30、60 μg·kg-1组,青龙木叶皂苷加纳洛酮组及生理盐水对照组。通过预先手术埋置的脑室套管向侧脑室注射青龙木叶皂苷,用辐射热甩尾法测定大鼠痛阈。结果:侧脑室注射3种不同剂量青龙木叶皂苷组的痛阈在注射5 min后与生理盐水对照组比较有不同程度的提高。 15 μg·kg-1组的痛阈虽然有提高,但与对照组比较差异无显著性(P>0.05); 30 μg·kg-1组的痛阈提高持续50 min,60 μg·kg-1组的痛阈提高可持续60 min以上,与对照组比较差异有显著性(P<0.05或P<0.01)。对照组大鼠的痛阈在60 min内无明显变化(P>0.05)。且青龙木叶皂苷镇痛效应可被纳洛酮所翻转。结论:青龙木叶皂苷具有较强镇痛效应及剂量-镇痛效应关系,其镇痛作用(痛阈升高)是通过脑内μ阿片受体实现的。

关键词: 痛觉测定, 痛阈, 动物, 实验

Abstract: Objective To investigate the analgesic effect of saponin of Pterocarpus Indicus(SPI). Methods Sixty rats were divided randomly into 5 groups (n=12):SPI with doses of 15,30,60 μg·kg-1 groups,SPI plus naloxone group and control group. Through the cannula penetrated into lateral cerebral ventricle, SPI was injected into lateral cerebral ventricle. Then,the tail-flick latency after the injection of SPI naloxone and saline was measured. Results The tail-flick latency was increased significantly 5 min after the injection(i.c.v.) of SPI,the amplitudes were corresponding with their doses. The effect of increasing of pain threshold in 30 μg·kg-1 SPI group was maintained until 50 min after the injection of SPI, 60 μg·kg-1SPI group was maintained until 60 min after the injection of SPI(P<0.01 or P<0.01).The pain threshold in control group was unchanged in 60 min (P>0.05). Naloxone could effectively antagonize the enhancement of the pain thresho ld induced by SPI.Conclusion SPI has a strong analgesic action and shows an obvious dose-effect relationship. The analgesic action may be mediated by μ opioid receptor in brain.

Key words: pain measurement, pain threshold, animals, laboratory

中图分类号: 

  • R977.1