Wang Y T, Bieger D, Neuman R S
Faculty of Medicine, Memorial University of Newfoundland, St. John's, Canada.
Brain Res. 1991 Dec 20;567(2):260-6. doi: 10.1016/0006-8993(91)90804-5.
The involvement of N-methyl-D-aspartate (NMDA) excitatory amino acid subtype receptors in synaptically driven excitatory responses of ambigual motoneurons was investigated in vivo and in vitro. In urethane-anaesthetized rats, fictive oesophageal peristalsis evoked by topical application of muscarine (0.05-0.5 nmol) to the dorsal surface of the solitarial complex (NTS) was reversibly blocked by ipsilateral intraambigual injection of DL-2-amino-7-phosphonoheptanoic acid (AP-7, 0.5-1.5 nM) and (+-)-3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP; 0.5-1.5 nM). In brainstem sagittal slices, post-synaptic potentials were recorded from neurons of the compact formation of the nucleus ambiguus (AMBc). Stimulation of presumptive NTS afferents elicited a complex excitatory postsynaptic potential (EPSP) which usually consisted of both a high-threshold fast (HTF) and a low-threshold slow (LTS) component. Bath perfusion with AP-7 (30-50 microM) and CPP (50 microM) selectively blocked the HTF without affecting the LTS component, while kynurenate (1 mM) and 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 5-10 microM) nonselectively suppressed both components. With sufficient stimulus strength, the EPSP generated a single spike arising from the HTF component. AP-7 (50 microM) either blocked the spike or increased the firing threshold. Furthermore, at the resting membrane potential, bath-applied NMDA induced a net inward current (269 +/- 189 pA) which had a negative slope in the range of -95 to -35 mV. In conclusion, NMDA receptors participate in solitario-ambigual synaptic transmission under physiological conditions and activation of these receptors is necessary for functional information transfer in this pathway.
在体内和体外研究了N-甲基-D-天冬氨酸(NMDA)兴奋性氨基酸亚型受体在疑核运动神经元突触驱动的兴奋性反应中的作用。在氨基甲酸乙酯麻醉的大鼠中,向孤束复合体(NTS)背表面局部应用毒蕈碱(0.05 - 0.5 nmol)诱发的虚构食管蠕动,被同侧疑核内注射DL-2-氨基-7-膦酰庚酸(AP-7,0.5 - 1.5 nM)和(±)-3-(2-羧基哌嗪-4-基)-丙基-1-膦酸(CPP;0.5 - 1.5 nM)可逆性阻断。在脑干矢状切片中,从疑核致密部(AMBc)的神经元记录突触后电位。刺激假定的NTS传入神经引发复杂的兴奋性突触后电位(EPSP),其通常由高阈值快速(HTF)和低阈值缓慢(LTS)成分组成。用AP-7(30 - 50 μM)和CPP(50 μM)进行浴灌流可选择性阻断HTF,而不影响LTS成分,而犬尿烯酸(1 mM)和6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX,5 - 10 μM)非选择性地抑制这两种成分。在足够的刺激强度下,EPSP产生一个由HTF成分引发的单个动作电位。AP-7(50 μM)要么阻断动作电位,要么提高放电阈值。此外,在静息膜电位下,浴灌流的NMDA诱导净内向电流(269±189 pA),其在 - 95至 - 35 mV范围内具有负斜率。总之,NMDA受体在生理条件下参与孤束-疑核突触传递,并且这些受体的激活对于该通路中的功能信息传递是必要的。