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多潘立酮在兔和人体中的前庭药理学

Vestibular pharmacology of domperidone in rabbits and man.

作者信息

Oosterveld W J

出版信息

ORL J Otorhinolaryngol Relat Spec. 1981;43(3):175-80. doi: 10.1159/000275537.

Abstract

Domperidone, administered to rabbits, is able t reduce the duration of a rotation-induced nystagmus. In human volunteers a similar effect was found in a double-blind study, in which single doses of 10, 20 and 40 mg were given orally. As electronystagmographic recordings were made during the rotation test at different time intervals after drug intake, the different dosages became comparable. The reduction of the nystagmus duration proved to be dose-dependent, whereas the peak velocity of the slow nystagmus component remained unchanged. The strongest effect of the drug appeared 60 min after intake, the effect lasted about 4 h. A mechanism of action different from that of cinnarizine and flunarizine is assumed because these drugs likewise influence the duration and the slow velocity component of nystagmus.

摘要

给兔子服用多潘立酮能够缩短旋转诱发的眼球震颤的持续时间。在一项双盲研究中,给人类志愿者口服10毫克、20毫克和40毫克的单剂量药物后,也发现了类似效果。由于在服药后的不同时间间隔进行旋转测试时进行了眼震电图记录,不同剂量具有了可比性。结果证明,眼球震颤持续时间的缩短具有剂量依赖性,而慢相眼球震颤成分的峰值速度保持不变。服药后60分钟药物效果最强,效果持续约4小时。假定其作用机制与桂利嗪和氟桂利嗪不同,因为这些药物同样会影响眼球震颤的持续时间和慢相速度成分。

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