Cercós Montserrat G, De-Miguel Francisco F, Trueta Citlali
Departamento de Neurofisiología, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Universidad Nacional Autónoma de México, Col. San Lorenzo Huipulco, Deleg. Tlalpan, C.P. 14370 México, Distrito Federal, México.
J Neurophysiol. 2009 Aug;102(2):1075-85. doi: 10.1152/jn.00107.2009. Epub 2009 Jun 17.
We studied autoinhibition produced immediately after synaptic serotonin (5-HT) release in identified leech Retzius neurons, cultured singly or forming synapses onto pressure-sensitive neurons. Cultured Retzius neurons are isopotential, thus allowing accurate recordings of synaptic events using intracellular microelectrodes. The effects of autoinhibition on distant neuropilar presynaptic endings were predicted from model simulations. Following action potentials (APs), cultured neurons produced a slow hyperpolarization with a rise time of 85.4 +/- 5.2 ms and a half-decay time of 252 +/- 17.4 ms. These inhibitory postpotentials were reproduced by the iontophoretic application of 5-HT and became depolarizing after inverting the transmembranal chloride gradient by using microelectrodes filled with potassium chloride. The inhibitory postpotentials were reversibly abolished in the absence of extracellular calcium and absent in reserpine-treated neurons, suggesting an autoinhibition due to 5-HT acting on autoreceptors coupled to chloride channels. The autoinhibitory responses increased the membrane conductance and decreased subsequent excitability. Increasing 5-HT release by stimulating with trains of ten pulses at 10 or 30 Hz produced 23 +/- 6 and 47 +/- 2% of AP failures, respectively. These failures were reversibly abolished by the serotonergic antagonist methysergide (140 muM). Moreover, reserpine-treated neurons had only 5 +/- 4% of failures during trains at 10 Hz. This percentage was increased to 35 +/- 4% by iontophoretic application of 5-HT. Increases in AP failures correlated with smaller postsynaptic currents. Model simulations predicted that the autoinhibitory chloride conductance reduces the amplitude of APs arriving at neuropilar presynaptic endings. Altogether, our results suggest that 5-HT autoinhibits its subsequent release by decreasing the excitability of presynaptic endings within the same neuron.
我们研究了在单个培养或与压敏神经元形成突触的已鉴定水蛭Retzius神经元中,突触5-羟色胺(5-HT)释放后立即产生的自身抑制作用。培养的Retzius神经元是等电位的,因此可以使用细胞内微电极准确记录突触事件。通过模型模拟预测了自身抑制对远处神经纤维网突触前末梢的影响。动作电位(APs)之后,培养的神经元产生缓慢的超极化,上升时间为85.4±5.2毫秒,半衰减时间为252±17.4毫秒。这些抑制性突触后电位通过5-HT的离子电泳施加得以重现,并且在使用充满氯化钾的微电极反转跨膜氯离子梯度后变为去极化。在无细胞外钙的情况下,抑制性突触后电位可逆地消失,在利血平处理的神经元中则不存在,这表明5-HT作用于与氯离子通道偶联的自身受体导致了自身抑制。自身抑制性反应增加了膜电导并降低了随后的兴奋性。以10或30赫兹的频率施加十次脉冲串刺激来增加5-HT释放,分别产生了23±6%和47±2%的AP失败率。这些失败被5-羟色胺能拮抗剂麦角新碱(140微摩尔)可逆地消除。此外,利血平处理的神经元在10赫兹的脉冲串刺激期间只有5±4%的失败率。通过5-HT的离子电泳施加,这个百分比增加到了35±4%。AP失败率的增加与较小的突触后电流相关。模型模拟预测,自身抑制性氯离子电导会降低到达神经纤维网突触前末梢的APs的幅度。总之,我们的结果表明,5-HT通过降低同一神经元内突触前末梢的兴奋性来自身抑制其随后的释放。