摘要
目的探讨白芷香豆素(Coumarin of Angelicae dahuricae,CAD)的镇痛作用机制.方法采用热板法,通过工具药观察CAD的镇痛作用与阿片受体和单胺类神经递质的关系;利用硝酸还原酶法检测CAD对甲醛所致伤害性疼痛模型小鼠血清一氧化氮(NitricOxide,NO)的含量.结果纳洛酮(5mg/kg)部分拮抗CAD(60mg/kg)的镇痛作用;利血平(4mg/kg)可以部分拮抗CAD(60mg/kg)的镇痛作用.CAD(30,60,120mg/kg)连续给药4d,使甲醛所致伤害性疼痛模型小鼠血清NO含量明显下降.结论CAD具有明显的镇痛,其镇痛作用与阿片受体和脑内单胺类神经递质有一定的关系.此外,明显减少NO的合成可能是其发挥镇痛作用的重要机制.
To observe the mechanism underlying analgesic effect of Coumarin of Angdicae dahuricae (CAD). Method The analgesic effect of CAD in mice was observed by using hot-plate, the relationship between analgesic effect of CAD and opioid receptor as well as monoamine neurotransmitter was observed through several agents;The concentration of nitric oxide(NO) in serum of analgesic mice induced by formaldehyde was measured with nitric reductase method. Results Naloxone (5 mg/kg)and reserpine (4 mg/kg) antagonized in part the analgesic effect of CAD (60 mg/kg) ;After four-day administration of CAD (30.60.120 mg/kg), the concentration of NO in serum of noeiceptive pain mice reduced Dy formaldehyde significantly decreased. Conclusion CAD has definite analgesic effect. There is a relationship between analgesic effect and opioid receptor as well as monoamine neurotransmitter. It is very important mechanism that CAD reduced production of NO.
出处
《北华大学学报(自然科学版)》
CAS
2009年第2期121-123,共3页
Journal of Beihua University(Natural Science)
基金
吉林省科技发展计划重点资助项目(20050913)
关键词
白芷香豆素
镇痛
阿片受体
NO
Coumarin of Angelicae dahuricae
Analgesic effect
Opioid receptor
NO