4.5 Article

Spatiotemporal visualization of deep brain stimulation-induced effects in the subthalamic nucleus

期刊

EUROPEAN JOURNAL OF NEUROSCIENCE
卷 36, 期 2, 页码 2252-2259

出版社

WILEY
DOI: 10.1111/j.1460-9568.2012.08086.x

关键词

computational modelling; finite element method; parameter settings; Parkinson's disease

资金

  1. BUPA foundation, UK
  2. BBSRC [BB/G006369/1] Funding Source: UKRI
  3. EPSRC [EP/D036364/1] Funding Source: UKRI
  4. MRC [G1100810, G0600168, G0701698, MC_U120036861] Funding Source: UKRI
  5. Biotechnology and Biological Sciences Research Council [BB/G006369/1] Funding Source: researchfish
  6. Engineering and Physical Sciences Research Council [EP/D036364/1] Funding Source: researchfish
  7. Medical Research Council [G0600168, MC_U120036861, G1100810, G0701698] Funding Source: researchfish

向作者/读者索取更多资源

Deep brain stimulation (DBS) is a successful surgical therapy used to treat the disabling symptoms of movement disorders such as Parkinsons disease. It involves the chronic stimulation of disorder-specific nuclei. However, the mechanisms that lead to clinical improvements remain unclear. Consequently, this slows the optimization of present-day DBS therapy and hinders its future development and application. We used a computational model to calculate the distribution of electric potential induced by DBS and study the effect of stimulation on the spiking activity of a subthalamic nucleus (STN) projection neuron. We previously showed that such a model can reveal detailed spatial effects of stimulation in the vicinity of the electrode. However, this multi-compartmental STN neuron model can fire in either a burst or tonic mode and, in this study, we hypothesized that the firing mode of the cell will have a major impact on the DBS-induced effects. Our simulations showed that the bursting model exhibits behaviour observed in studies of high-frequency stimulation of STN neurons, such as the presence of a silent period at stimulation offset and frequency-dependent stimulation effects. We validated the model by simulating the clinical parameter settings used for a Parkinsonian patient and showed, in a patient-specific anatomical model, that the region of affected tissue is consistent with clinical observations of the optimal DBS site. Our results demonstrated a method of quantitatively assessing neuronal changes induced by DBS, to maximize therapeutic benefit and minimize unwanted side effects.

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