Weiss B, Santelli S
Science. 1978 May 19;200(4343):799-801. doi: 10.1126/science.417399.
In two cebus (Cebus albifrons) monkeys given weekly oral doses of 0.25 milligram of haloperidol per kilogram, movement disorders appeared 1 to 8 hours after drug administration following the tenth weekly dose. These disorders included oral movements, peculiar postures, writhing, and stretching. Such reactions faded in intensity after the next two doses. Increasing the dose to 0.5 milligram per kilogram has elicited the disorders reliably after each weekly dose for almost 2 years. Similar reactions also developed in a squirrel monkey (Saimiri sciurea) treated weekly with haloperidol and in a third cebus monkey previously maintained for a year on a regimen of 0.25 milligram of haloperidol per kilogram on 5 days per week. These findings suggest an experimental model for determining the etiology of drug-induced movement disorders. They also suggest an unrecognized clinical problem.
给两只白额卷尾猴(Cebus albifrons)每周口服每千克0.25毫克氟哌啶醇,在第十次每周给药后,给药后1至8小时出现运动障碍。这些障碍包括口腔运动、奇特姿势、扭动和伸展。在接下来的两次给药后,这种反应的强度逐渐减弱。将剂量增加到每千克0.5毫克后,在近2年的每次每周给药后都可靠地引发了这些障碍。在每周接受氟哌啶醇治疗的松鼠猴(Saimiri sciurea)以及之前每周5天、以每千克0.25毫克氟哌啶醇的方案维持了一年的第三只白额卷尾猴中也出现了类似反应。这些发现提示了一种用于确定药物性运动障碍病因的实验模型。它们还提示了一个未被认识到的临床问题。