Abstract

Thalamic deep brain stimulation (DBS) is an effective treatment for tremor, but the mechanisms of action remain unclear. Previous studies of human thalamic neurons to noted transient rebound bursting activity followed by prolonged inhibition after cessation of high frequency extracellular stimulation, and the present study sought to identify the mechanisms underlying this response. Recordings from 13 thalamic neurons exhibiting low threshold spike (LTS) bursting to brief periods of extracellular stimulation were made during surgeries to implant DBS leads in 6 subjects with Parkinson's disease. The response immediately after cessation of stimulation included a short epoch of burst activity, followed by a prolonged period of silence before a return to LTS bursting. A computational model of a population of thalamocortical relay neurons and presynaptic axons terminating on the neurons was used to identify cellular mechanisms of the observed responses. The model included the actions of neuromodulators through inhibition of a non-pertussis toxin sensitive K+ current (IKL), activation of a pertussis toxin sensitive K+ current (IKG), and a shift in the activation curve of the hyperpolarization-activated cation current (Ih). The model replicated well the measured responses, and the prolonged inhibition was associated most strongly with changes in IKG while modulation of IKL or Ih had minimal effects on post-stimulus inhibition suggesting that neuromodulators released in response to high frequency stimulation are responsible for mediating the post-stimulation bursting and subsequent long duration silence of thalamic neurons. The modeling also indicated that the axons of the model neurons responded robustly to suprathreshold stimulation despite the inhibitory effects on the soma. The findings suggest that during DBS the axons of thalamocortical neurons are activated while the cell bodies are inhibited thus blocking the transmission of pathological signals through the network and replacing them with high frequency regular firing.

Highlights

  • High frequency deep brain stimulation (HFS) in the ventralis intermedius (Vim) nucleus of the thalamus is an established therapy for the treatment of tremor in movement disorders, including essential tremor (ET) and Parkinson’s disease (PD)

  • Despite the effects of neuromodulators on the post-stimulus behavior of thalamic neurons, the axons of the model thalamocortical relay neurons responded robustly to suprathreshold stimulation in the period during stimulation, and activity in these axons was driven by the stimulation pulses during HFS. These results suggest that the effects of neuromodulators released in response to HFS are responsible for the post-stimulation bursting and subsequent long inhibition of firing of thalamic neurons

  • The predominant response of human thalamic neurons immediately after cessation of HFS included a short epoch of burst activity, followed by a prolonged period of silence

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Summary

Introduction

High frequency deep brain stimulation (HFS) in the ventralis intermedius (Vim) nucleus of the thalamus is an established therapy for the treatment of tremor in movement disorders, including essential tremor (ET) and Parkinson’s disease (PD). A hallmark of the effects of thalamic stimulation on tremor is the sensitivity to stimulation frequency (reviewed in [1]). Maximum tremor suppression is typically observed only when the frequency of stimulation is greater than 90 Hz, and lower frequencies are ineffective or may exacerbate symptoms [2,3,4]. To gain a better understanding of possible mechanisms that may underly neuronal responses to thalamic DBS, in the present study we recorded extracellularly the responses of human thalamic neurons in human subjects following brief periods of extracellular stimulation and subsequently used computer simulations in a biophysical model of thalamic stimulation to identify candidate cellular and ionic mechanisms that might explain the observed responses

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