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作 者:周文华[1,2] 朱波[1,2] 谢小虎[1,2] 张亚海[1,2] 刘惠芬[1,2] 杨国栋[1,2]
机构地区:[1]宁波市微循环与莨菪类药研究所 [2]宁波戒毒研究中心
出 处:《中国药物依赖性杂志》1999年第2期95-97,共3页Chinese Journal of Drug Dependence
基 金:浙江省卫生厅青年人才基金;宁波市青年基金
摘 要:本文检测了吗啡依赖大鼠脊髓和脑干一氧化氮合酶(NOs)活力,一氧化氮(NO)以及cGMP含量。结果显示吗啡依赖大鼠脊髓NOs活力,NO和cGMP含量较正常对照组降低,脑干中NOs活力轻度降低,而NO和cGMP含量降低。纳洛酮激发戒断症状后大鼠脊髓和脑干NOs活力,NO以及cGMP含量急剧升高。NOs抑制剂L-N-硝基精氨酸甲酯(L-NAME)处理可以抑制大鼠吗啡戒断反应,同时减少脊髓和脑干NO含量。结果表明吗啡戒断反应与脊髓和脑干的NO-cGMP途径的兴奋有关。The present results showed that the activities of nitric oxide synthase (NOs) in morphine dependent rats were 1.3 nmolmin-1g-1s 0.27 nmolmin-1g-1 tissue in spinal cord which was lower than that of the activities of NOs (2.9 nmolmin-1g-1s 0.51 nmolmin-1g-1,n=5,P<0.05) in control animals, and the activities of NOs in stem were decreased slightly in morphine dependent rats,while the activities of NOs in spinal cord and stem in morphine withdrawal rats precipitated by naloxone were both increased significantly compared with morphine dependent rats. The NO2-/NO3-(the end products of NO) levels and cGMP contents in spinal cord and stem in morphine dependent rats were decreased compared with the control animals,and during morphine withdrawal the NO levels and cGMP contents were increased over those of morphine dependent rats. L-N-nitroarginine methyl-ester(L-NAME),a competitive inhibitor of NOs, was administered as a single injection (10 mgkg-1,ip) 1 hour before the injection of naloxone in morphine dependent rats, it was revealed that L-NAME reduced the total ratings of withdrawal signs, and also decreased the NO production in spinal cord and stem. The data indicated that the excitement of NO-cGMP pathway in spinal cord and stem may play an important role in mediating the process of morphine withdrawal.
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