Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors

The flow of cortical information through the basal ganglia is a complex spatiotemporal pattern of increased and decreased firing. The striatum is the biggest input nucleus to the basal ganglia and the aim of this study was to assess the role of inhibitory GABAA and glycine receptors in regulating sy...

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Main Authors: Louise eAdermark, Rhona B Clarke, Mia eEricson, Bo eSöderpalm
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-10-01
Series:Frontiers in Systems Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnsys.2011.00085/full
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author Louise eAdermark
Rhona B Clarke
Mia eEricson
Bo eSöderpalm
author_facet Louise eAdermark
Rhona B Clarke
Mia eEricson
Bo eSöderpalm
author_sort Louise eAdermark
collection DOAJ
description The flow of cortical information through the basal ganglia is a complex spatiotemporal pattern of increased and decreased firing. The striatum is the biggest input nucleus to the basal ganglia and the aim of this study was to assess the role of inhibitory GABAA and glycine receptors in regulating synaptic activity in the dorsolateral (DLS) and ventral striatum (nucleus accumbens, nAc). Local field potential recordings from coronal brain slices of juvenile and adult Wistar rats showed that GABAA receptors and strychnine-sensitive glycine receptors are tonically activated and inhibit excitatory input to the DLS and to the nAc. Strychnine-induced disinhibition of glutamatergic transmission was insensitive to the muscarinic receptor inhibitor scopolamine (10 µM), inhibited by the nicotinic acetylcholine receptor antagonist mecamylamine (10 µM) and blocked by GABAA receptor inhibitors, suggesting that tonically activated glycine receptors depress excitatory input to the striatum through modulation of cholinergic and GABAergic neurotransmission. As an end-product example of striatal GABAergic output in vivo we measured dopamine release in the DLS and nAc by microdialysis in the awake and freely moving rat. Reversed dialysis of bicuculline (50 μM in perfusate) only increased extrasynaptic dopamine levels in the nAc, while strychnine administered locally (200 μM in perfusate) decreased dopamine output by 60% in both the DLS and nAc. Our data suggest that GABAA and glycine receptors are tonically activated and modulate striatal transmission in a partially sub-region specific manner.
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spelling doaj.art-daf3cdb9c7a543cfa6fc6447b015c75d2022-12-21T22:40:42ZengFrontiers Media S.A.Frontiers in Systems Neuroscience1662-51372011-10-01510.3389/fnsys.2011.0008513753Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptorsLouise eAdermark0Rhona B Clarke1Mia eEricson2Bo eSöderpalm3University of GothenburgUniversity of GothenburgUniversity of GothenburgUniversity of GothenburgThe flow of cortical information through the basal ganglia is a complex spatiotemporal pattern of increased and decreased firing. The striatum is the biggest input nucleus to the basal ganglia and the aim of this study was to assess the role of inhibitory GABAA and glycine receptors in regulating synaptic activity in the dorsolateral (DLS) and ventral striatum (nucleus accumbens, nAc). Local field potential recordings from coronal brain slices of juvenile and adult Wistar rats showed that GABAA receptors and strychnine-sensitive glycine receptors are tonically activated and inhibit excitatory input to the DLS and to the nAc. Strychnine-induced disinhibition of glutamatergic transmission was insensitive to the muscarinic receptor inhibitor scopolamine (10 µM), inhibited by the nicotinic acetylcholine receptor antagonist mecamylamine (10 µM) and blocked by GABAA receptor inhibitors, suggesting that tonically activated glycine receptors depress excitatory input to the striatum through modulation of cholinergic and GABAergic neurotransmission. As an end-product example of striatal GABAergic output in vivo we measured dopamine release in the DLS and nAc by microdialysis in the awake and freely moving rat. Reversed dialysis of bicuculline (50 μM in perfusate) only increased extrasynaptic dopamine levels in the nAc, while strychnine administered locally (200 μM in perfusate) decreased dopamine output by 60% in both the DLS and nAc. Our data suggest that GABAA and glycine receptors are tonically activated and modulate striatal transmission in a partially sub-region specific manner.http://journal.frontiersin.org/Journal/10.3389/fnsys.2011.00085/fullBasal GangliaBicucullineNucleus AccumbensStrychnineratdorsolateral striatum
spellingShingle Louise eAdermark
Rhona B Clarke
Mia eEricson
Bo eSöderpalm
Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors
Frontiers in Systems Neuroscience
Basal Ganglia
Bicuculline
Nucleus Accumbens
Strychnine
rat
dorsolateral striatum
title Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors
title_full Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors
title_fullStr Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors
title_full_unstemmed Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors
title_short Subregion-specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and GABAA receptors
title_sort subregion specific modulation of excitatory input and dopaminergic output in the striatum by tonically activated glycine and gabaa receptors
topic Basal Ganglia
Bicuculline
Nucleus Accumbens
Strychnine
rat
dorsolateral striatum
url http://journal.frontiersin.org/Journal/10.3389/fnsys.2011.00085/full
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