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      Group II metabotropic glutamate receptors inhibit cAMP-dependent protein kinase-mediated enhancemednt of tetrodotoxin-resistant sodium currents in mouse dorsal root ganglion neurons.

      Neuroscience Letters
      Amino Acids, pharmacology, Analysis of Variance, Animals, Animals, Newborn, Cells, Cultured, Colforsin, Cyclic AMP-Dependent Protein Kinases, physiology, Dose-Response Relationship, Drug, Drug Interactions, Excitatory Amino Acid Agonists, Excitatory Amino Acid Antagonists, Ganglia, Spinal, cytology, drug effects, Membrane Potentials, Mice, NAV1.7 Voltage-Gated Sodium Channel, Neurons, Neuropeptides, Pyrrolidines, Receptors, Metabotropic Glutamate, Sodium Channels, Thiocarbamates, Time Factors, Xanthenes

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          Abstract

          Tetrodotoxin (TTX)-resistant sodium currents are important in nociception and nociceptive sensitization, which is partially due to their cAMP/protein kinase A (PKA)-mediated enhancement. Here we studied the effects of group II mGluR activation on TTX-resistant sodium currents in cultured mouse dorsal root ganglion (DRG) neurons. Activation of adenylyl cyclase with forskolin caused an increase in the amplitude of TTX-R currents and a leftward shift of the activation curve. When neurons were treated with ammonium pyrrolidinedithiocarbamate (APDC), a selective group II mGluR agonist, both the forskolin-induced increase in current amplitude and the shift of activation curve were blocked. LY341495, a group II mGluR antagonist, prevented these inhibitory effects of APDC. Our results suggest that group II mGluRs can negatively regulate TTX-R sodium currents in mouse DRG neurons.

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