Metabotropic glutamate receptor subtype 1 regulates sodium currents in rat neocortical pyramidal neurons
Autor: | Edmond Carlier, Dominique Debanne, Laure Fronzaroli-Molinieres, Patrice Déglise, Sami Boudkkazi, Valérie Sourdet, Norbert Ankri |
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Rok vydání: | 2006 |
Předmět: |
Agonist
0303 health sciences Physiology Chemistry medicine.drug_class Sodium channel Metabotropic glutamate receptor 6 Glutamate receptor 03 medical and health sciences chemistry.chemical_compound Glutamatergic 0302 clinical medicine Metabotropic glutamate receptor medicine Metabotropic glutamate receptor 1 Neurotransmitter Neuroscience 030217 neurology & neurosurgery 030304 developmental biology |
Zdroj: | The Journal of Physiology. 577:141-154 |
ISSN: | 0022-3751 |
Popis: | Brain sodium channels (NaChs) are regulated by various neurotransmitters such as acetylcholine, serotonin and dopamine. However, it is not known whether NaCh activity is regulated by glutamate, the principal brain neurotransmitter. We show here that activation of metabotropic glutamate receptor (mGluR) subtype 1 regulates fast transient (INaT) and persistent Na+ currents (INaP) in cortical pyramidal neurons. A selective agonist of group I mGluR, (S)-3,5-dihydroxyphenylglycine (DHPG), reduced action potential amplitude and decreased INaT. This reduction was blocked when DHPG was applied in the presence of selective mGluR1 antagonists. The DHPG-induced reduction of the current was accompanied by a shift of both the inactivation curve of INaT and the activation curve of INaP. These effects were dependent on the activation of PKC. The respective role of these two regulatory processes on neuronal excitability was determined by simulating transient and persistent Na+ conductances (GNaT and GNaP) with fast dynamic-clamp techniques. The facilitated activation of GNaP increased excitability near the threshold, but, when combined with the down-regulation of GNaT, repetitive firing was strongly decreased. Consistent with this finding, the mGluR1 antagonist LY367385 increased neuronal excitability when glutamatergic synaptic activity was stimulated with high external K+. We conclude that mGluR1-dependent regulation of Na+ current depresses neuronal excitability, which thus might constitute a novel mechanism of homeostatic regulation acting during intense glutamatergic synaptic activity. |
Databáze: | OpenAIRE |
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