Dietzel I, Heinemann U, Lux H D
Department of Neurophysiology, Max-Planck-Institute for Psychiatry, Planegg-Martinsried, Federal Republic of Germany.
Glia. 1989;2(1):25-44. doi: 10.1002/glia.440020104.
The aim of this investigation is to estimate the contribution of spatial glial K+ buffer currents to extracellular K+ homeostasis during enhanced neuronal activity. Neuronal hyperactivity was induced by electrical stimulation of the cortical surface or the ventrobasal thalamic nuclei of cats (5-50 Hz, 0.1-0.2 ms, two to three times threshold stimulation intensity, 5-20 s). The accompanying slow field potential changes were recorded simultaneously across the grey matter with vertical assemblies of eight micropipettes glued 300 microns apart. Using the Poisson equation, the amplitudes of the underlying current sources and sinks were calculated. The current source densities depended on the depth of recording, frequency, strength, and duration of the stimulation. Current sinks, corresponding to a removal of 0.1-0.5 mmoles of monovalent cations per liter of brain tissue and second from the extracellular space, were observed in middle cortical layers, whereas sources appeared at superficial and deeper sites. These sinks and sources might represent K+ moved across glial membranes by spatial buffer currents. The consequences of glial buffer currents of this magnitude were investigated with model calculations. It turned out that measurements of electrolyte and volume changes of the extracellular space (Dietzel et al. Exp. Brain Res. 40:432-439, 1980; Exp. Brain Res. 46:73-84, 1982) could only partially be explained by spatial buffer currents of this magnitude. Comparison of the calculated values with intracellular measurements in neurons and glial cells (Coles et al. Ann. N.Y. Acad. Sci. 481:303-317, 1986; Ballanyi et al. J. Physiol. 382:159-174, 1987) suggests that spatial buffering combines with an approximately equimolar KCl transport and, depending on the preparation, also K+/Na+-exchange across glial membranes.
本研究的目的是评估在神经元活动增强期间,空间胶质细胞钾离子缓冲电流对细胞外钾离子稳态的贡献。通过电刺激猫的皮质表面或腹侧基底丘脑核来诱导神经元活动亢进(5 - 50赫兹,0.1 - 0.2毫秒,阈刺激强度的两到三倍,5 - 20秒)。同时,用八个间隔300微米粘贴在一起的微电极垂直阵列,在灰质上同步记录伴随的慢场电位变化。利用泊松方程,计算了潜在电流源和电流汇的幅度。电流源密度取决于记录深度、刺激频率、强度和持续时间。在皮质中间层观察到电流汇,相当于每升脑组织每秒从细胞外空间移除0.1 - 0.5毫摩尔单价阳离子,而电流源出现在表层和深层部位。这些电流汇和电流源可能代表通过空间缓冲电流跨胶质细胞膜移动的钾离子。通过模型计算研究了这种量级的胶质细胞缓冲电流的后果。结果表明,细胞外空间电解质和体积变化的测量结果(迪策尔等人,《实验脑研究》40:432 - 439,1980年;《实验脑研究》46:73 - 84,1982年)只能部分地由这种量级的空间缓冲电流来解释。将计算值与神经元和胶质细胞的细胞内测量值进行比较(科尔斯等人,《纽约科学院学报》481:303 - 317,1986年;巴兰伊等人,《生理学杂志》382:159 - 174,1987年)表明,空间缓冲与近似等摩尔的氯化钾转运相结合,并且根据实验准备情况,还包括跨胶质细胞膜的钾离子/钠离子交换。