Coordinated reset stimulation in a large-scale model of the STN-GPe circuit

被引:50
|
作者
Ebert, Martin [1 ,2 ]
Hauptmann, Christian [1 ]
Tass, Peter A. [1 ,3 ,4 ]
机构
[1] Forschungszentrum Julich, Inst Neurosci & Med Neuromodulat, D-52425 Julich, Germany
[2] Univ Cologne, Inst Nucl Phys, Dept Phys, D-50931 Cologne, Germany
[3] Stanford Univ, Dept Neurosurg, Stanford, CA 94305 USA
[4] Univ Cologne, Dept Neuromodulat, D-50931 Cologne, Germany
关键词
deep brain stimulation; high-performance computing; coordinated reset stimulation; electrode design; DEEP-BRAIN-STIMULATION; HIGH-FREQUENCY STIMULATION; EXTERNAL GLOBUS-PALLIDUS; SUBTHALAMIC NUCLEUS; PARKINSONS-DISEASE; BASAL GANGLIA; STIMULUS PARAMETERS; CORRELATED ACTIVITY; BETA OSCILLATIONS; ACTIVITY PATTERNS;
D O I
10.3389/fncom.2014.00154
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Synchronization of populations of neurons is a hallmark of several brain diseases. Coordinated reset (CR) stimulation is a model-based stimulation technique which specifically counteracts abnormal synchrony by desynchronization. Electrical CR stimulation, e.g., for the treatment of Parkinson's disease (PD), is administered via depth electrodes. In order to get a deeper understanding of this technique, we extended the top-down approach of previous studies and constructed a large-scale computational model of the respective brain areas. Furthermore, we took into account the spatial anatomical properties of the simulated brain structures and incorporated a detailed numerical representation of 2 . 10(4) simulated neurons. We simulated the subthalamic nucleus (STN) and the globus pallidus externus (GPe). Connections within the STN were governed by spike-timing dependent plasticity (STDP). In this way, we modeled the physiological and pathological activity of the considered brain structures. In particular, we investigated how plasticity could be exploited and how the model could be shifted from strongly synchronized (pathological) activity to strongly desynchronized (healthy) activity of the neuronal populations via CR stimulation of the STN neurons. Furthermore, we investigated the impact of specific stimulation parameters especially the electrode position on the stimulation outcome. Our model provides a step forward toward a biophysically realistic model of the brain areas relevant to the emergence of pathological neuronal activity in PD. Furthermore, our model constitutes a test bench for the optimization of both stimulation parameters and novel electrode geometries for efficient CR stimulation.
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页数:20
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