Herreras O, Largo C, Ibarz J M, Somjen G G, Martín del Río R
Departamento Investigación, Hospital Ramón y Cajal, Madrid, Spain.
J Neurosci. 1994 Nov;14(11 Pt 2):7087-98. doi: 10.1523/JNEUROSCI.14-11-07087.1994.
To detect what initiates spreading depression (SD), the early prodromal events were investigated in hippocampal CA1 of urethane-anesthetized rats. SD was provoked by microdialysis or focal microinjection of high-K+ solution. Extracellular DC potentials and extracellular potassium concentration ([K+]o) were recorded, and spontaneous and evoked potentials analyzed for current source-density (CSD). In the front of an approaching SD wave, several seconds before the onset of the typical sustained negative potential shift (delta Vo) and the increased [K+]o, fast electrical activity was detected. This consisted initially of small rhythmic (60-70 Hz) sawtooth wavelets, which then gave way to a shower of population spikes (PSs) of identical frequency. Prodromal wavelets and PSs were synchronized over considerable distances in the tissue. Sawtooth wavelets were identified as pacemakers of the prodromal PS burst. Simultaneous recording at three depths revealed that the spontaneous prodromal PSs occurred exactly in phase in dendrites and somata whereas synaptically transmitted PSs arose first in the proximal dendrites and were conducted from there into the soma membrane. During a spike burst, stratum (st.) pyramidale served as current sink, while in the proximal sublayer of st. radiatum spike-sinks gave way to spike sources that grew larger as the sinks in st. pyramidale began to subside. Blocking synaptic transmission did not abolish the prodromal spike burst, yet repetitive orthodromic activation inhibited it without altering the subsequent SD waveform. Complex changes in cell excitability were detected even before fast spontaneous activities. We concluded that, in the initial evolution of SD, changes in neuron function precede the regenerating depolarization by several seconds. We propose that the opening of normally closed electric junctions among neurons can best explain the long-distance synchronization and the flow current that occurs in the leading edge of a propagating wave of SD.
为了检测引发扩散性抑制(SD)的因素,我们在氨基甲酸乙酯麻醉的大鼠海马CA1区研究了早期前驱事件。通过微透析或局部微量注射高钾溶液诱发SD。记录细胞外直流电位和细胞外钾离子浓度([K+]o),并分析自发和诱发电位的电流源密度(CSD)。在即将到来的SD波前沿,在典型的持续负电位偏移(δVo)和[K+]o增加之前几秒,检测到快速电活动。这最初由小的节律性(60-70Hz)锯齿状小波组成,随后被相同频率的群体锋电位(PSs)阵雨所取代。前驱小波和PSs在组织中相当长的距离内同步。锯齿状小波被确定为前驱PS爆发的起搏器。在三个深度同时记录显示,自发前驱PSs在树突和胞体中精确地同相发生,而突触传递的PSs首先出现在近端树突中,并从那里传导到胞体膜。在锋电位爆发期间,锥体层(st.)作为电流汇,而在辐射层(st.)的近端亚层中,锋电位汇被锋电位源所取代,随着锥体层中的汇开始消退,锋电位源变得更大。阻断突触传递并没有消除前驱锋电位爆发,但重复性的顺向激活抑制了它,而不改变随后的SD波形。甚至在快速自发活动之前就检测到细胞兴奋性的复杂变化。我们得出结论,在SD的初始演变中,神经元功能的变化比再生性去极化提前几秒。我们提出,神经元之间正常关闭的电连接的开放最能解释在SD传播波前沿发生的长距离同步和电流流动。