[HTML][HTML] Sixty hertz neurostimulation amplifies subthalamic neural synchrony in Parkinson's disease

Z Blumenfeld, A Velisar, M Miller Koop, BC Hill… - PLoS …, 2015 - journals.plos.org
Z Blumenfeld, A Velisar, M Miller Koop, BC Hill, LA Shreve, EJ Quinn, C Kilbane, H Yu…
PLoS One, 2015journals.plos.org
High frequency subthalamic nucleus (STN) deep brain stimulation (DBS) improves the
cardinal motor signs of Parkinson's disease (PD) and attenuates STN alpha/beta band
neural synchrony in a voltage-dependent manner. While there is a growing interest in the
behavioral effects of lower frequency (60 Hz) DBS, little is known about its effect on STN
neural synchrony. Here we demonstrate for the first time that during intra-operative 60 Hz
STN DBS, one or more bands of resting state neural synchrony were amplified in the STN in …
High frequency subthalamic nucleus (STN) deep brain stimulation (DBS) improves the cardinal motor signs of Parkinson’s disease (PD) and attenuates STN alpha/beta band neural synchrony in a voltage-dependent manner. While there is a growing interest in the behavioral effects of lower frequency (60 Hz) DBS, little is known about its effect on STN neural synchrony. Here we demonstrate for the first time that during intra-operative 60 Hz STN DBS, one or more bands of resting state neural synchrony were amplified in the STN in PD. We recorded intra-operative STN resting state local field potentials (LFPs) from twenty-eight STNs in seventeen PD subjects after placement of the DBS lead (model 3389, Medtronic, Inc.) before and during three randomized neurostimulation sets (130 Hz/1.35V, 130 Hz/2V, 60 Hz/2V). During 130 Hz/2V DBS, baseline (no DBS) STN alpha (8 – 12 Hz) and beta (13 – 35 Hz) band power decreased (N=14, P < 0.001 for both), whereas during 60 Hz/2V DBS, alpha band and peak frequency power increased (P = 0.012, P = 0.007, respectively). The effect of 60 Hz/2V DBS opposed that of power-equivalent (130 Hz/1.35V) DBS (alpha: P < 0.001, beta: P = 0.006). These results show that intra-operative 60 Hz STN DBS amplified whereas 130 Hz STN DBS attenuated resting state neural synchrony in PD; the effects were frequency-specific. We demonstrate that neurostimulation may be useful as a tool to selectively modulate resting state resonant bands of neural synchrony and to investigate its influence on motor and non-motor behaviors in PD and other neuropsychiatric diseases.
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