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

被引:20
|
作者
Yang, DN
Gereau, RW
机构
[1] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
[2] Baylor Coll Med, Div Neurosci, Houston, TX 77030 USA
关键词
mGluR; forskolin; mGlu2; pain; nociception; inflammation; primary sensory neuron;
D O I
10.1016/j.neulet.2003.11.074
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:159 / 162
页数:4
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