Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice
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...
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todo:paper_00223077_v85_n2_p659_Cepeda2023-10-03T14:30:59Z Facilitated glutamatergic transmission in the striatum of D2 dopamine receptor-deficient mice Cepeda, C. Hurst, R.S. Altemus, K.L. Flores-Hernández, J. Calvert, C.R. Jokel, E.S. Grandy, D.K. Low, M.J. Rubinstein, M. Ariano, M.A. Levine, M.S. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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 Cepeda, C. Hurst, R.S. Altemus, K.L. Flores-Hernández, J. Calvert, C.R. Jokel, E.S. Grandy, D.K. Low, M.J. Rubinstein, M. Ariano, M.A. Levine, M.S. 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. |
| format |
JOUR |
| author |
Cepeda, C. Hurst, R.S. Altemus, K.L. Flores-Hernández, J. Calvert, C.R. Jokel, E.S. Grandy, D.K. Low, M.J. Rubinstein, M. Ariano, M.A. Levine, M.S. |
| author_facet |
Cepeda, C. Hurst, R.S. Altemus, K.L. Flores-Hernández, J. Calvert, C.R. Jokel, E.S. Grandy, D.K. Low, M.J. Rubinstein, M. Ariano, M.A. Levine, M.S. |
| author_sort |
Cepeda, C. |
| 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 |
| url |
http://hdl.handle.net/20.500.12110/paper_00223077_v85_n2_p659_Cepeda |
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