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右美沙芬可减轻体内新皮质缺血性神经元损伤。

Dextromethorphan reduces neocortical ischemic neuronal damage in vivo.

作者信息

George C P, Goldberg M P, Choi D W, Steinberg G K

机构信息

Division of Neurosurgery, Stanford University Medical Center, CA 94305-5327.

出版信息

Brain Res. 1988 Feb 9;440(2):375-9. doi: 10.1016/0006-8993(88)91011-6.

Abstract

The dextrorotatory morphinan dextromethorphan (DM), a clinically tested antagonist of the N-methyl-D-aspartate (NMDA) receptor-channel complex, was tested in an in vivo model of acute transient focal cerebral ischemia. Rabbits were randomly assigned to pretreatment with a 20 mg/kg i.v. bolus followed by 10 mg/kg/h of 0.4% DM in normal saline (NS), or with an equivalent volume of NS alone. They then underwent 1 h occlusion of the left internal carotid artery an anterior cerebral artery followed by 4 h of reperfusion. DM-treated animals showed a significant decrease in the percentage of severe neocortical ischemic neuronal damage (10.5%), as compared to NS-treated animals (49.6%).

摘要

右旋吗啡喃右美沙芬(DM)是一种经临床测试的N-甲基-D-天冬氨酸(NMDA)受体通道复合物拮抗剂,在急性短暂性局灶性脑缺血的体内模型中进行了测试。将兔子随机分为两组,一组预先静脉注射20mg/kg的负荷剂量,随后以10mg/kg/h的速度静脉输注0.4%的DM生理盐水溶液(NS),另一组仅给予等量的NS。然后对兔子进行1小时的左侧颈内动脉和大脑前动脉闭塞,随后再灌注4小时。与接受NS治疗的动物(49.6%)相比,接受DM治疗的动物严重新皮质缺血性神经元损伤的百分比显著降低(10.5%)。

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