The pedunculopontine nucleus as an additional target for deep brain stimulation
The pedunculopontine nucleus has been suggested as a target for DBS. In this paper we propose a single compartment computational model for a PPN Type I cell and compare its dynamic behavior with experimental data. The model shows bursts after a period of hyperpolarization and spontaneous firing at 8...
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Veröffentlicht in: | Neural networks 2011-08, Vol.24 (6), p.617-630 |
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Sprache: | eng |
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Zusammenfassung: | The pedunculopontine nucleus has been suggested as a target for DBS. In this paper we propose a single compartment computational model for a PPN Type I cell and compare its dynamic behavior with experimental data. The model shows bursts after a period of hyperpolarization and spontaneous firing at 8 Hz. Bifurcation analysis of the single PPN cell shows bistability of fast and slow spiking solutions for a range of applied currents. A network model for STN, GPe and GPi produces basal ganglia output that is used as input for the PPN cell. The conductances for projections from the STN and the GPi to the PPN are determined from experimental data. The resulting behavior of the PPN cell is studied under normal and Parkinsonian conditions of the basal ganglia network. The effect of high frequency stimulation of the STN is considered as well as the effect of combined high frequency stimulation of the STN and the PPN at various frequencies. The relay properties of the PPN cell demonstrate that the combined high frequency stimulation of STN and low frequency (10 Hz, 25 Hz, 40 Hz) stimulation of PPN hardly improves the effect of exclusive STN stimulation. Moreover, PPN–DBS at low stimulation amplitude has a better effect than at higher stimulation amplitude. The effect of PPN output on the basal ganglia is investigated, in particular the effect of STN–DBS and/or PPN–DBS on the pathological firing pattern of STN and GPe cells. PPN–DBS eliminates the pathological firing pattern of STN and GPe cells, whereas STN–DBS and combined STN–DBS and PPN–DBS eliminate the pathological firing pattern only from STN cells. |
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ISSN: | 0893-6080 1879-2782 |
DOI: | 10.1016/j.neunet.2011.03.007 |