摘要
目的:探讨士的宁敏感的甘氨酸受体(strychnine-sensitive glycine receptor,GlyR)与吸入麻醉药异氟烷、恩氟烷、七氟烷、乙醚镇痛作用的关系。方法:小鼠腹腔注射(i.p.)吸入麻醉药,以甩尾法和福尔马林法观察鞘内注射(i.t.)士的宁(strychnine,Stry)对吸入麻醉药镇痛作用的影响。结果:在甩尾实验中,Stry0.1μgi.t.能降低乙醚镇痛小鼠的甩尾潜伏期(tail flick latency,TFL)(P<0.05),但对异氟烷、恩氟烷、七氟烷镇痛小鼠的TFL无明显影响(P>0.05)。Stry0.2,0.4μg则使四种吸入麻醉药镇痛小鼠的TFL降低(P<0.05)。福尔马林实验中,腹腔注射吸入麻醉药能产生明显的镇痛作用,但Stry(0.1,0.2,0.4μg)i.t.对上述4种麻醉药的镇痛作用均无明显影响。结论:脊髓GlyR可能是吸入麻醉药抗热刺激伤害的重要靶位,但不影响吸入麻醉药对化学刺激的镇痛作用。
To investigate the relationship between strychnine-sensitive glycine receptor(GlyR) and the analgesic effects of aether, enflurane, isoflurane and sevoflurane. Methods: The mice model of analgesia was established by intraperitoneally injecting (i, p. ) appropriate doses of aether, enflurane, isoflurane or sevoflurane, different doses of strychnine (Stry) were intrathecally ( i. t. ) injected and then the effects on the pain threshold of the mice treated with inhalation anesthetics were obsered using tailwithdrawal test and formalin test. Results: In tail-withdrawal test, the increase of tail flick latency(TFL) induced by four inhalation anesthetics was abolished by strychnine (i. t. ). In formalin test, inhalation anesthetics ( i. p. ) significantly increased the pain threshold of mice, but Stry (0.1,0.2,0.4 μg) did not affect the pain threshold of mice treated with four inhalation anesthetics. Conclusion: Spinal GlyR mediates the analgesic effects of aether, enflurane, isoflurane, sevoflurane in tail-withdrawal test but not in formalin test,
出处
《中国疼痛医学杂志》
CAS
CSCD
北大核心
2007年第5期293-297,共5页
Chinese Journal of Pain Medicine
基金
国家自然科学基金资助项目(No30471657
39970715)
江苏省自然科学基金资助项目(NoBK2001143)
广西医疗卫生计划课题(Z2005199)
关键词
士的宁
甘氨酸受体
吸入麻醉药
镇痛
机制
Strychnine
Glycine receptor
Inhalation anesthetic
Analgesia
Mechanism