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大鼠迟发性运动障碍假定模型中丘脑底核损伤的影响。

Effects of subthalamic nucleus lesions in a putative model of tardive dyskinesia in the rat.

作者信息

Stoessl A J, Rajakumar N

机构信息

Clinical Neurological Sciences, University of Western Ontario, London, Ontario, Canada.

出版信息

Synapse. 1996 Nov;24(3):256-61. doi: 10.1002/(SICI)1098-2396(199611)24:3<256::AID-SYN8>3.0.CO;2-D.

Abstract

The effects of bilateral excitotoxic lesions of the subthalamic nucleus on vacuous chewing movements induced by chronic neuroleptic therapy were examined in the rat. Fluphenazine decanoate (25 mg/kg i.m.q 3 weeks x 24 weeks) induced vacuous chewing movements, as previously described. This response was suppressed to control levels in animals tested 1-3 weeks following bilateral infusion of quinolinic acid (100 nmol/1 microliter per side) into the subthalamic nucleus. Subthalamic nucleus lesions resulted in increased locomotion and sniffing in neuroleptic-naive animals, but these responses were suppressed by concomitant neuroleptic treatment. As vacuous chewing movements induced by chronic neuroleptics are considered to be analogous to tardive dyskinesia in humans, our findings lend further support to the importance of the subthalamic nucleus in the regulation of orofacial movements and suggest that tardive dyskinesia may, in part, be related to altered activity in this structure. This, in turn, suggests that current models of basal ganglia function are inadequate to account for certain pathological states and require re-examination.

摘要

在大鼠中研究了双侧丘脑底核兴奋性毒性损伤对慢性抗精神病药物治疗诱发的空嚼运动的影响。癸酸氟奋乃静(25mg/kg,肌肉注射,每3周一次,共24周)如前所述诱发了空嚼运动。在双侧向丘脑底核注入喹啉酸(每侧100nmol/1微升)后1-3周进行测试的动物中,这种反应被抑制到对照水平。丘脑底核损伤导致未使用过抗精神病药物的动物运动和嗅探增加,但这些反应被同时进行的抗精神病药物治疗所抑制。由于慢性抗精神病药物诱发的空嚼运动被认为类似于人类的迟发性运动障碍,我们的研究结果进一步支持了丘脑底核在调节口面部运动中的重要性,并表明迟发性运动障碍可能部分与该结构的活动改变有关。这反过来又表明,目前的基底神经节功能模型不足以解释某些病理状态,需要重新审视。

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