Article
Deep brain stimulation of the centromedian-parafascicular nucleus affects apomorphine-induced alteration of striatal fast and medium spiking interneurons in a rat model
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Published: | June 18, 2018 |
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Objective: Striatal dysfunction has been related to the pathophysiology of tics in Tourette’s syndrome (TS). Deep brain stimulation (DBS) of the centromedian-parafascicular (CM-Pf) nucleus, which projects to the striatum, is used clinically to alleviate tics in TS. Apomorphine-induced deficient sensorimotor gating in rats has been used to model TS in rats. We recently showed that DBS of the rat CM-Pf may alleviate this behavioral change.We here investigated the effect of CM-Pf stimulation on single neuronal activity and oscillatory activity of striatal fast and medium spiking interneurons in this model.
Methods: We recorded dorsomedial striatum (DS-Str) medium spiny neurons (MSNs) and fast-spiking interneurons (FSIs) single unit (SU) activity together with local field potentials (LFPs) and sensory motor electro-corticogram (SMCtx- ECoG)under urethane anesthesia (1.4 g/kg, i.p.) in rats before and after apomorphine injection (1mg/kg). Thereafter, 60 sec CM-Pf-DBS (130 Hz, 100 µA current, with 120 µs biphasic square wave pulses) was applied and the neuronal activity recorded.
Results: While apomorphine had little effect on striatal single unit activity, CM-Pf DBS significantly increased the firing rate of putative FSIs and decreased the percentage of spikes in burst in the DM-Str. Injection of apomorphine increased the theta (4-8Hz) frequency coherences of SMCtx- ECoG with DM-Str-LFPs and the spike phase-locking to theta oscillatory activity, which was both reduced by CM-Pf DBS.
Conclusion: Our findings suggest that CM-Pf DBS modulates neuronal activity in the striatum in the context of a rat model showing traits of TS. These neuronal interactions allow to better understand the mechanisms of CM-Pf DBS on the striatum in deficient sensorimotor gating.