Deep brain stimulation of the subthalamic or entopeduncular nucleus attenuates vacuous chewing movements in a rodent model of tardive dyskinesia

被引:19
作者
Creed, Meaghan [1 ,2 ]
Hamani, Clement [1 ,5 ]
Nobrega, Jose N. [1 ,2 ,3 ,4 ]
机构
[1] Ctr Addict & Mental Hlth, Neuroimaging Res Sect, Toronto, ON M5T 1R8, Canada
[2] Univ Toronto, Dept Pharmacol & Toxicol, Toronto, ON, Canada
[3] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[4] Univ Toronto, Dept Psychol, Toronto, ON M5S 1A1, Canada
[5] Toronto Western Hosp, Div Neurosurg, Toronto, ON M5T 2S8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
DBS; Subthalamic nucleus; Entopeduncular nucleus; Globus pallidus; Tardive dyskinesias; Chronic haloperidol; Antipsychotic drugs; High-frequency stimulation; DOPAMINE-D-2 RECEPTOR OCCUPANCY; GLOBUS-PALLIDUS INTERNUS; PARKINSONS-DISEASE; ORAL DYSKINESIAS; PROXIMAL TREMOR; HALOPERIDOL; RATS; DISORDERS; DYSTONIA; PATHOPHYSIOLOGY;
D O I
10.1016/j.euroneuro.2010.06.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Deep brain stimulation (DBS) has recently emerged as a potential intervention for treatment-resistant tardive dyskinesia (TD). Despite promising case reports, no consensus exists as yet regarding optimal stimulation parameters or neuroanatomical target for DBS in TD. Here we report the use of DBS in an animal model of TD. We applied DBS (100 mu A) acutely to the entopeduncular nucleus (EPN) or subthalamic nucleus (STN) in rats with well established vacuous chewing movements (VCMs) induced by 12 weeks of haloperidol (HAL) treatment. Stimulation of the STN or EPN resulted in significant reductions in VCM counts at frequencies of 30, 60 or 130 Hz. In the STN DBS groups, effects were significantly more pronounced at 130 Hz than at lower frequencies, whereas at the EPN the three frequencies were equipotent. Unilateral stimulation at 130 Hz was also effective when applied to either nucleus. These results suggest that stimulation of either the EPN or STN significantly alleviates oral dyskinesias induced by chronic HAL. The chronic HAL VCM model preparation may be useful to explore mechanisms underlying DBS effects in drug-induced dyskinesias. (C) 2010 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:393 / 400
页数:8
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