Jørgensen H A, Andreassen O A, Hole K
Department of Psychiatry, Section Sandviken Hospital, University of Bergen, Sandviken, Norway.
Psychopharmacology (Berl). 1994 Sep;116(1):89-92. doi: 10.1007/BF02244876.
Tardive dyskinesia (TD) is a serious and sometimes irreversible side-effect to long-term neuroleptic treatment. In order to find predictors for development of TD, it would be of interest to known whether susceptibility to develop acute side-effects increases the risk of TD development. The study investigated in female Sprague-Dawley rats the relationship between haloperidol-induced acute motor effects, assessed by means of the grid test and the open field test, and the chronic motor effect assessed as vacuous chewing movements (VCM). The doses of haloperidol were 1.2, 2.4 and 4.8 mg/kg IP in the acute experiments and haloperidol decanoate 38 mg/kg per 4 weeks IM in the chronic experiment. The VCM obtained at different timepoints during the 24 weeks of chronic treatment were highly correlated. However, no correlation was found between the motor effects in the acute and the chronic experiments. The study does not indicate any connection between susceptibility to acute side-effects on neuroleptics and later development of TD.
迟发性运动障碍(TD)是长期使用抗精神病药物治疗产生的一种严重且有时不可逆的副作用。为了找到TD发生的预测因素,了解对急性副作用的易感性是否会增加TD发生的风险将是很有意义的。该研究在雌性斯普拉格-道利大鼠中调查了通过网格试验和旷场试验评估的氟哌啶醇诱导的急性运动效应与作为空嚼运动(VCM)评估的慢性运动效应之间的关系。在急性实验中,氟哌啶醇的剂量为1.2、2.4和4.8mg/kg腹腔注射,在慢性实验中,癸酸氟哌啶醇的剂量为每4周38mg/kg肌肉注射。在慢性治疗的24周内不同时间点获得的VCM高度相关。然而,在急性和慢性实验的运动效应之间未发现相关性。该研究未表明对抗精神病药物急性副作用的易感性与TD后期发生之间存在任何联系。