Fortin G, Champagnat J
Institut Alfred Fessard, CNRS, Gif sur Yvette, France.
Brain Res. 1993 Dec 10;630(1-2):125-35. doi: 10.1016/0006-8993(93)90650-c.
The pattern of synaptic interactions between neurons of the nucleus tractus solitarius (NTS) has been analyzed using whole cell recording in rat brainstem slices. Following tractus solitarius (TS) stimulation 15/55 neurons presented a prolonged (up to 300 ms) increased excitability (PIE neurons) and 40/55 neurons presented a prolonged (up to 200 ms) reduced excitability (PRE neurons). In the absence of afferent sensory input all neurons showed spontaneous synaptic activity. Ongoing synaptic activity in PIE cells was glutamatergic and characterized by the absence of detectable inhibitory potentials while in PRE cells it was 90% GABAergic and 10% glutamatergic. Glutamatergic synaptic currents in PIE cells and GABAergic synaptic currents in PRE were studied using probability density and intensity functions. Distribution of time intervals between synaptic events indicated the latter were generated, in both PIE and PRE cells, by two simultaneous processes: (1) a close to Poisson process generating independent events; and (2) a subsidiary re-excitatory process generating synaptic events separated by intervals shorter than 20 ms. Blockade of glutamatergic transmission by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX; 10 microM) or blockade of action potentials by tetrodotoxin (TTX; 1 microM) suppressed the subsidiary process. In conclusion, we propose that PIE cells (1) form a re-excitatory network contributing to generation of excitatory activity in the NTS and (2) are located presynaptically with respect to PRE cells.
利用大鼠脑干切片的全细胞记录技术,对孤束核(NTS)神经元之间的突触相互作用模式进行了分析。在刺激孤束(TS)后,55个神经元中有15个呈现出兴奋性延长(长达300毫秒)增强(PIE神经元),55个神经元中有40个呈现出兴奋性延长(长达200毫秒)降低(PRE神经元)。在没有传入感觉输入的情况下,所有神经元均表现出自发性突触活动。PIE细胞中的持续突触活动是谷氨酸能的,其特征是未检测到抑制性电位,而PRE细胞中的持续突触活动90%是GABA能的,10%是谷氨酸能的。使用概率密度和强度函数研究了PIE细胞中的谷氨酸能突触电流和PRE细胞中的GABA能突触电流。突触事件之间的时间间隔分布表明,在PIE细胞和PRE细胞中,突触事件都是由两个同时发生的过程产生的:(1)一个接近泊松过程产生独立事件;(2)一个辅助的再兴奋过程产生间隔短于20毫秒的突触事件。用6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX;10微摩尔)阻断谷氨酸能传递或用河豚毒素(TTX;1微摩尔)阻断动作电位可抑制辅助过程。总之,我们提出PIE细胞(1)形成一个再兴奋网络,有助于在NTS中产生兴奋性活动;(2)相对于PRE细胞位于突触前。