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spelling paper:paper_00223077_v85_n2_p659_Cepeda2023-06-08T14:49:13Z Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice 4 aminopyridine bicuculline methiodide dopamine 2 receptor dopamine 4 receptor glutamate receptor quinpirole receptor subtype sulpiride animal tissue article controlled study corpus striatum dendritic spine depolarization immunocytochemistry mouse nerve cell stimulation neurotransmission nonhuman priority journal synapse voltage clamp 4-Aminopyridine Animals Corpus Striatum Dopamine Electrophysiology Glutamic Acid Immunohistochemistry Membranes Mice Mice, Inbred C57BL Mice, Knockout Neurons Receptors, Dopamine D2 Synapses Synaptic Transmission Dopamine (DA) receptors play an important role in the modulation of excitability and the responsiveness of neurons to activation of excitatory amino acid receptors in the striatum. In the present study, we utilized mice with genetic deletion of D2 or D4 DA receptors and their wild-type (WT) controls to examine if the absence of either receptor subtype affects striatal excitatory synaptic activity. Immunocytochemical analysis verified the absence of D2 or D4 protein expression in the striatum of receptor-deficient mutant animals. Sharp electrode current- and whole cell patch voltage-clamp recordings were obtained from slices of receptor-deficient and WT mice. Basic membrane properties were similar in D2 and D4 receptor-deficient mutants and their respective WT controls. In current-clamp recordings in WT animals, very little low-amplitude spontaneous synaptic activity was observed. The frequency of these spontaneous events was increased slightly in D2 receptor-deficient mice. In addition, large-amplitude depolarizations were observed in a subset of neurons from only the D2 receptor-deficient mutants. Bath application of the K+ channel blocker 4-aminopyridine (100 μM) and bicuculline methiodide (10 μM, to block synaptic activity due to activation of GABAA receptors) markedly increased spontaneous synaptic activity in receptor-deficient mutants and WTs. Under these conditions, D2 receptor-deficient mice displayed significantly more excitatory synaptic activity than their WT controls, while there was no difference between D4 receptor-deficient mice and their controls. In voltage-clamp recordings, there was an increase in frequency of spontaneous glutamate receptor-mediated inward currents without a change in mean amplitude in D2 receptor-deficient mutants. In WT mice, activation of D2 family receptors with quinpirole decreased spontaneous excitatory events and conversely sulpiride, a D2 receptor antagonist, increased activity. In D2 receptor-deficient mice, sulpiride had very little net effect. Morphologically, a subpopulation of medium-sized spiny neurons from D2 receptor-deficient mice displayed decreased dendritic spines compared with cells from WT mice. These results provide evidence that D2 receptors play an important role in the regulation of glutamate receptor-mediated activity in the corticostriatal or thalamostriatal pathway. These receptors may function as gatekeepers of glutamate release or of its subsequent effects and thus may protect striatal neurons from excessive excitation. 2001 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223077_v85_n2_p659_Cepeda http://hdl.handle.net/20.500.12110/paper_00223077_v85_n2_p659_Cepeda
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 4 aminopyridine
bicuculline methiodide
dopamine 2 receptor
dopamine 4 receptor
glutamate receptor
quinpirole
receptor subtype
sulpiride
animal tissue
article
controlled study
corpus striatum
dendritic spine
depolarization
immunocytochemistry
mouse
nerve cell stimulation
neurotransmission
nonhuman
priority journal
synapse
voltage clamp
4-Aminopyridine
Animals
Corpus Striatum
Dopamine
Electrophysiology
Glutamic Acid
Immunohistochemistry
Membranes
Mice
Mice, Inbred C57BL
Mice, Knockout
Neurons
Receptors, Dopamine D2
Synapses
Synaptic Transmission
spellingShingle 4 aminopyridine
bicuculline methiodide
dopamine 2 receptor
dopamine 4 receptor
glutamate receptor
quinpirole
receptor subtype
sulpiride
animal tissue
article
controlled study
corpus striatum
dendritic spine
depolarization
immunocytochemistry
mouse
nerve cell stimulation
neurotransmission
nonhuman
priority journal
synapse
voltage clamp
4-Aminopyridine
Animals
Corpus Striatum
Dopamine
Electrophysiology
Glutamic Acid
Immunohistochemistry
Membranes
Mice
Mice, Inbred C57BL
Mice, Knockout
Neurons
Receptors, Dopamine D2
Synapses
Synaptic Transmission
Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
topic_facet 4 aminopyridine
bicuculline methiodide
dopamine 2 receptor
dopamine 4 receptor
glutamate receptor
quinpirole
receptor subtype
sulpiride
animal tissue
article
controlled study
corpus striatum
dendritic spine
depolarization
immunocytochemistry
mouse
nerve cell stimulation
neurotransmission
nonhuman
priority journal
synapse
voltage clamp
4-Aminopyridine
Animals
Corpus Striatum
Dopamine
Electrophysiology
Glutamic Acid
Immunohistochemistry
Membranes
Mice
Mice, Inbred C57BL
Mice, Knockout
Neurons
Receptors, Dopamine D2
Synapses
Synaptic Transmission
description Dopamine (DA) receptors play an important role in the modulation of excitability and the responsiveness of neurons to activation of excitatory amino acid receptors in the striatum. In the present study, we utilized mice with genetic deletion of D2 or D4 DA receptors and their wild-type (WT) controls to examine if the absence of either receptor subtype affects striatal excitatory synaptic activity. Immunocytochemical analysis verified the absence of D2 or D4 protein expression in the striatum of receptor-deficient mutant animals. Sharp electrode current- and whole cell patch voltage-clamp recordings were obtained from slices of receptor-deficient and WT mice. Basic membrane properties were similar in D2 and D4 receptor-deficient mutants and their respective WT controls. In current-clamp recordings in WT animals, very little low-amplitude spontaneous synaptic activity was observed. The frequency of these spontaneous events was increased slightly in D2 receptor-deficient mice. In addition, large-amplitude depolarizations were observed in a subset of neurons from only the D2 receptor-deficient mutants. Bath application of the K+ channel blocker 4-aminopyridine (100 μM) and bicuculline methiodide (10 μM, to block synaptic activity due to activation of GABAA receptors) markedly increased spontaneous synaptic activity in receptor-deficient mutants and WTs. Under these conditions, D2 receptor-deficient mice displayed significantly more excitatory synaptic activity than their WT controls, while there was no difference between D4 receptor-deficient mice and their controls. In voltage-clamp recordings, there was an increase in frequency of spontaneous glutamate receptor-mediated inward currents without a change in mean amplitude in D2 receptor-deficient mutants. In WT mice, activation of D2 family receptors with quinpirole decreased spontaneous excitatory events and conversely sulpiride, a D2 receptor antagonist, increased activity. In D2 receptor-deficient mice, sulpiride had very little net effect. Morphologically, a subpopulation of medium-sized spiny neurons from D2 receptor-deficient mice displayed decreased dendritic spines compared with cells from WT mice. These results provide evidence that D2 receptors play an important role in the regulation of glutamate receptor-mediated activity in the corticostriatal or thalamostriatal pathway. These receptors may function as gatekeepers of glutamate release or of its subsequent effects and thus may protect striatal neurons from excessive excitation.
title Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
title_short Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
title_full Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
title_fullStr Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
title_full_unstemmed Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
title_sort facilitated glutamatergic transmission in the striatum of d2 dopamine receptor-deficient mice
publishDate 2001
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223077_v85_n2_p659_Cepeda
http://hdl.handle.net/20.500.12110/paper_00223077_v85_n2_p659_Cepeda
_version_ 1768543500902596608