Muscarinic presynaptic inhibition of neostriatal glutamatergic afferents is mediated by Q-type Ca2+ channels
Muscarinic presynaptic inhibition of neostriatal glutamatergic afferents is mediated by Q-type Ca2+ channels
复制标题
DOI：
10.1016/s0361-9230(99)00061-1
复制
发表时间：
1999-07-01
影响因子：
3.8
通讯作者：
Bargas, J
中科院分区：
文献类型：
--
作者：
Barral, J;Galarraga, E;Bargas, J
Cholinergic presynaptic inhibition was investigated on neostriatal glutamatergic transmission, Paired pulse facilitation (PPF) of orthodromic population spikes (PS) were used to construct a concentration-response relationship for muscarine on presynaptic inhibition, Muscarine had an effect proportional to its extracellular concentration with an EC50 (mean a standard estimation error) of: 2.5 +/- 1.5 nM, and a maximal effect (saturation) of 245 +/- 16%, Several peptidic toxins against some voltage-gated Ca2+-channels increased PPF indicating that the Ca2+-channels they block participate in transmitter release. However, neither 1 mu M omega-conotoxin GVIA, a specific blocker of N-type Ca2+-channels, nor 10-30 nM omega-agatoxinTK, a selective blocker of P-type Ca2+-channels, were able to occlude muscarine's effect on presynaptic inhibition. Nevertheless, 100-400 nM omega-agatoxinTK occluded muscarine's action on PPF in a dose-dependent manner. These results are consistent with Q-type Ca2+-channels mediating muscarinic presynaptic inhibition of neostriatal afferents, (C) 1999 Elsevier Science Inc.
