Khakh B S, Henderson G
Department of Pharmacology, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, UK.
Mol Pharmacol. 1998 Aug;54(2):372-8. doi: 10.1124/mol.54.2.372.
ATP-gated cation channels (P2X receptors) exist on the soma of proprioceptive neurons in the trigeminal mesencephalic nucleus (MNV) in the brain stem. However, these pseudomonopolar neurons seem to receive no synaptic input to their soma; we therefore hypothesized that in MNV neurons, the P2X receptors of importance may be those located on their central terminal projections. Here, we show in trigeminal mesencephalic motor nucleus neurons, which receive their major input from the MNV, that both exogenous ATP (1 mM) and high frequency focal stimulation to evoke endogenous ATP release enhanced the frequency of spontaneous fast excitatory postsynaptic currents (EPSCs) with no change in their amplitude. The enhancement was reduced by the antagonists suramin (300 microM) and pyridoxal-phosphate-6-azophenyl-2',4'-disulfonic acid (30 microM) and persisted when action potential conduction was blocked with tetrodotoxin (1 microM). Thus, functional P2X receptors are expressed on nerve terminals in the brain stem, where they increase the spontaneous release of glutamate onto trigeminal mesencephalic motor nucleus neurons.
三磷酸腺苷门控阳离子通道(P2X受体)存在于脑干三叉神经中脑核(MNV)本体感觉神经元的胞体上。然而,这些假单极神经元的胞体似乎没有接受突触输入;因此我们推测,在MNV神经元中,重要的P2X受体可能位于其中枢终末投射上。在此,我们在三叉神经中脑运动核神经元中发现,这些神经元主要接收来自MNV的输入,外源性三磷酸腺苷(1 mM)以及用于诱发内源性三磷酸腺苷释放的高频局部刺激,均可增加自发快速兴奋性突触后电流(EPSC)的频率,而其幅度不变。拮抗剂苏拉明(300 microM)和磷酸吡哆醛 - 6 - 偶氮苯 - 2',4'-二磺酸(30 microM)可减弱这种增强作用,而当用河豚毒素(1 microM)阻断动作电位传导时,这种增强作用依然存在。因此,功能性P2X受体在脑干的神经末梢上表达,在那里它们增加谷氨酸向三叉神经中脑运动核神经元的自发释放。