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作 者:曹君利[1] 丁海雷[2] 张励才[3] 段世明[3] 曾因明[3]
机构地区:[1]徐州医学院附属医院麻醉科 [2]Physiological Laboratory of Hypoxia,Health Science Center,Shanghai Institutes ofr biological Science,Chinese Academy of Sciences,Shanghai200031,China [3]江苏省麻醉学重点实验室
出 处:《Acta Pharmacologica Sinica》2002年第8期685-690,共6页中国药理学报(英文版)
摘 要:AIM: To investigate the roles of pretreatment with midazolam on morphine withdrawal in mice and rats. METHODS: Acute and chronic morphine dependence and naloxone-precipitated withdrawal models were em-ployed in the present study. Cyclic adenosine monophosphate (AMP) content and Fos protein expression were measured by radioimmunoassay and immunocytochemistry, respectively. RESULTS: Coadministration of midazolam (2 mg/kg, ip) and morphine prevented the development of both acute and chronic morphine dependence in mice. Compared to saline-morphine group (3.0, 95 % confidence limits: 1.9-4.3 mg/kg), ED50 of naloxone-precipiated withdrawal jumping increased significantly in midazolam-morphine group (10.4, 95 % confidence limits: 8.5-12.3 mg/kg) in acute morphine-dependent mice (P<0.01). Pretreatment with midazolam lowered the number and incidence of naloxone-precepiated withdrawal jumping and prevented loss in body weight in chronic mor-phine-dependent mice (P<0.01). Midazolam-pretreatment inhibited the increase of Fos protein expression, not cyclic AMP content, in rat spinal cord during morphine withdrawal. CONCLUSION: Midazolam suppresses morphine withdrawal response by inhibiting hypersensitization of the spinal cord neurons, and this effect may not be mediated by cAMP pathway.目的:研究咪哒唑仑对小鼠和大鼠吗啡戒断反应的影响.方法:实验中采用急性和慢性吗啡依赖和纳洛酮催促戒断模型.使用放免法测定cAMP含量,免疫组织化学方法观察Fos蛋白表达变化.结果:合用咪哒唑仑和吗啡可抑制小鼠急性和慢性吗啡依赖的发展.在急性吗啡依赖小鼠,咪哒唑仑-吗啡组纳络酮催促跳跃的ED_(50)(10.4,8.5-12.3 mg/kg)明显大于生理盐水-吗啡组(3.0,1.9-4.3 mg/kg)(P<0.01).在慢性吗啡依赖小鼠,咪哒唑仑-吗啡组纳络酮催促跳跃的发生率和跳跃次数明显低于生理盐水-吗啡组(P<0.01).预先使用咪哒唑仑抑制吗啡戒断大鼠脊髓Fos蛋白表达,但不能抑制脊髓cAMP含量的增加.结论:咪哒唑仑通过抑制脊髓神经元敏感化减轻吗啡戒断反应,cAMP信号转导通路不参与介导这一效应.
关 键 词:MIDAZOLAM MORPHINE substance withdrawal syndrome adenosine cyclic monophosphate GABA proto-oncogene proteins c-fos spinal cord
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