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混沌去同步化作为深部脑刺激的治疗机制。

Chaotic desynchronization as the therapeutic mechanism of deep brain stimulation.

机构信息

Department of Biology, University of Texas at San Antonio San Antonio, TX, USA.

出版信息

Front Syst Neurosci. 2011 Jun 21;5:50. doi: 10.3389/fnsys.2011.00050. eCollection 2011.

DOI:10.3389/fnsys.2011.00050
PMID:21734868
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3122072/
Abstract

High frequency deep-brain stimulation of the subthalamic nucleus (deep brain stimulation, DBS) relieves many of the symptoms of Parkinson's disease in humans and animal models. Although the treatment has seen widespread use, its therapeutic mechanism remains paradoxical. The subthalamic nucleus is excitatory, so its stimulation at rates higher than its normal firing rate should worsen the disease by increasing subthalamic excitation of the globus pallidus. The therapeutic effectiveness of DBS is also frequency and intensity sensitive, and the stimulation must be periodic; aperiodic stimulation at the same mean rate is ineffective. These requirements are not adequately explained by existing models, whether based on firing rate changes or on reduced bursting. Here we report modeling studies suggesting that high frequency periodic excitation of the subthalamic nucleus may act by desynchronizing the firing of neurons in the globus pallidus, rather than by changing the firing rate or pattern of individual cells. Globus pallidus neurons are normally desynchronized, but their activity becomes correlated in Parkinson's disease. Periodic stimulation may induce chaotic desynchronization by interacting with the intrinsic oscillatory mechanism of globus pallidus neurons. Our modeling results suggest a mechanism of action of DBS and a pathophysiology of Parkinsonism in which synchrony, rather than firing rate, is the critical pathological feature.

摘要

高频深部脑刺激丘脑底核(深部脑刺激,DBS)可缓解人类和动物模型中许多帕金森病的症状。尽管该治疗方法已得到广泛应用,但其治疗机制仍存在矛盾。丘脑底核是兴奋性的,因此其刺激频率高于其正常放电频率,通过增加苍白球对丘脑底核的兴奋,应该会使疾病恶化。DBS 的治疗效果也与频率和强度有关,刺激必须是周期性的;相同平均速率的非周期性刺激无效。这些要求不能用现有的基于放电率变化或减少爆发的模型来充分解释。在这里,我们报告的建模研究表明,高频周期性刺激丘脑底核可能通过使苍白球神经元的放电去同步化而不是通过改变单个细胞的放电率或模式来发挥作用。苍白球神经元通常是去同步的,但在帕金森病中它们的活动变得相关。周期性刺激可能通过与苍白球神经元的内在振荡机制相互作用而诱导混沌去同步化。我们的建模结果表明 DBS 的作用机制和帕金森病的病理生理学,其中同步性而不是放电率是关键的病理特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/e754dac61ed1/fnsys-05-00050-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/9da78e0f2ccd/fnsys-05-00050-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/1292c2922ae7/fnsys-05-00050-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/fdaf6a16a07c/fnsys-05-00050-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/e754dac61ed1/fnsys-05-00050-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/9da78e0f2ccd/fnsys-05-00050-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/1292c2922ae7/fnsys-05-00050-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/fdaf6a16a07c/fnsys-05-00050-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796e/3122072/e754dac61ed1/fnsys-05-00050-g004.jpg

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