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- W2899333822 abstract "Deep-brain stimulation (DBS) of the globus pallidus pars interna (GPi) is a highly effective therapy for movement disorders, yet its mechanism of action remains controversial. Inhibition of local neurons because of release of GABA from afferents to the GPi is a proposed mechanism in patients. Yet, high-frequency stimulation (HFS) produces prolonged membrane depolarization mediated by cholinergic neurotransmission in endopeduncular nucleus (EP, GPi equivalent in rodent) neurons. We applied HFS while recording neuronal firing from an adjacent electrode during microelectrode mapping of GPi in awake patients (both male and female) with Parkinson disease (PD) and dystonia. Aside from after-suppression and no change in neuronal firing, high-frequency microstimulation induced after-facilitation in 38% (26/69) of GPi neurons. In neurons displaying after-facilitation, 10 s HFS led to an immediate decrease of bursting in PD, but not dystonia patients. Moreover, the changes of bursting patterns in neurons with after-suppression or no change after HFS, were similar in both patient groups. To explore the mechanisms responsible, we applied HFS in EP brain slices from rats of either sex. As in humans, HFS in EP induced two subtypes of after-excitation: excitation or excitation with late inhibition. Pharmacological experiments determined that the excitation subtype, induced by lower charge density, was dependent on glutamatergic transmission. HFS with higher charge density induced excitation with late inhibition, which involved cholinergic modulation. Therefore HFS with different charge density may affect the local neurons through multiple synaptic mechanisms. The cholinergic system plays a role in mediating the after-facilitatory effects in GPi neurons, and because of their modulatory nature, may provide a basis for both the immediate and delayed effects of GPi-DBS. We propose a new model to explain the mechanisms of DBS in GPi.SIGNIFICANCE STATEMENT Deep-brain stimulation (DBS) in the globus pallidus pars interna (GPi) improves Parkinson disease (PD) and dystonia, yet its mechanisms in GPi remain controversial. Inhibition has been previously described and thought to indicate activation of GABAergic synaptic terminals, which dominate in GPi. Here we report that 10 s high-frequency microstimulation induced after-facilitation of neural firing in a substantial proportion of GPi neurons in humans. The neurons with after-facilitation, also immediately reduced their bursting activities after high-frequency stimulation in PD, but not dystonia patients. Based on these data and further animal experiments, a mechanistic hypothesis involving glutamatergic, GABAergic, and cholinergic synaptic transmission is proposed to explain both short- and longer-term therapeutic effects of DBS in GPi." @default.
- W2899333822 created "2018-11-09" @default.
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- W2899333822 date "2018-10-29" @default.
- W2899333822 modified "2023-10-14" @default.
- W2899333822 title "Long-Lasting Electrophysiological After-Effects of High-Frequency Stimulation in the Globus Pallidus: Human and Rodent Slice Studies" @default.
- W2899333822 cites W1489708744 @default.
- W2899333822 cites W1516023815 @default.
- W2899333822 cites W1565164110 @default.
- W2899333822 cites W1768450208 @default.
- W2899333822 cites W1779371161 @default.
- W2899333822 cites W1891730382 @default.
- W2899333822 cites W1905563481 @default.
- W2899333822 cites W1965302959 @default.
- W2899333822 cites W1970581037 @default.
- W2899333822 cites W1970985512 @default.
- W2899333822 cites W1982827121 @default.
- W2899333822 cites W1991106943 @default.
- W2899333822 cites W1991869255 @default.
- W2899333822 cites W1993938009 @default.
- W2899333822 cites W1995798947 @default.
- W2899333822 cites W1996679986 @default.
- W2899333822 cites W1996999362 @default.
- W2899333822 cites W1997979881 @default.
- W2899333822 cites W1998850305 @default.
- W2899333822 cites W2008686569 @default.
- W2899333822 cites W2017852553 @default.
- W2899333822 cites W2021380404 @default.
- W2899333822 cites W2023796931 @default.
- W2899333822 cites W2023922059 @default.
- W2899333822 cites W2029754211 @default.
- W2899333822 cites W2030033126 @default.
- W2899333822 cites W2033771777 @default.
- W2899333822 cites W2035946761 @default.
- W2899333822 cites W2043535426 @default.
- W2899333822 cites W2050688876 @default.
- W2899333822 cites W2051004303 @default.
- W2899333822 cites W2051101627 @default.
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- W2899333822 cites W2060756235 @default.
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- W2899333822 cites W2066016314 @default.
- W2899333822 cites W2071751312 @default.
- W2899333822 cites W2073383779 @default.
- W2899333822 cites W2075189228 @default.
- W2899333822 cites W2080760355 @default.
- W2899333822 cites W2091046222 @default.
- W2899333822 cites W2092420754 @default.
- W2899333822 cites W2095976264 @default.
- W2899333822 cites W2116153309 @default.
- W2899333822 cites W2117365703 @default.
- W2899333822 cites W2123208606 @default.
- W2899333822 cites W2125380728 @default.
- W2899333822 cites W2126454291 @default.
- W2899333822 cites W2131171101 @default.
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- W2899333822 cites W2144589096 @default.
- W2899333822 cites W2144869674 @default.
- W2899333822 cites W2166562076 @default.
- W2899333822 cites W2171090485 @default.
- W2899333822 cites W2174555113 @default.
- W2899333822 cites W21769058 @default.
- W2899333822 cites W2181278871 @default.
- W2899333822 cites W2305277766 @default.
- W2899333822 cites W2316653764 @default.
- W2899333822 cites W2345463283 @default.
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- W2899333822 doi "https://doi.org/10.1523/jneurosci.0785-18.2018" @default.
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