The equilibration time course of [K+]0 in cat cortex

SummarySteady state and transient values of intracortical potassium were measured with K+ sensitive microelectrodes. Resting intracortical K+ activity is low and resembles that of cerebrospinal fluid. Elevation of intracortical K+ was brought about by electrophoretic injection of K+ by a constant current source from a KCl containing micropipette at fixed distances from the recording electrode. The intracortical K+ responses to electrophoretic K+ injection were compared with those in a medium of 150 mM/l NaCl plus 3 mM/l KCl. The dependence of intracortical K+ steady state levels on electrophoretic currents is nearly linear, but the K+ response in the cortex was about six times higher than in saline. Half times (T1/2) of the rising and falling phases of K+ during current steps were found to be prolonged by the same degree in the cortex. The distribution of [K+]0 appears to be dominated by free diffusion with an apparent diffusion coefficient of 1/6 that in the medium. Primarily diffusional redistribution may also apply to K+ which is released by direct cortical stimulation. K+ released by brief stimulation distributes faster than K+ during and after prolonged continuous stimulation with average T1/2 of 1.2 and 3.0 sec respectively in accordance with diffusion from instantaneous and continuous point sources. For small [K+]0 changes, deviations from diffusional kinetics were found to be about one-fifth of absolute [K+]0 values and became predominant at times longer than 10 T1/2. They can be ascribed to K+ uptake mechanisms. DC recorded cortical surface potentials reveal close relations to the slopes of intracortical potassium activity.

[1]  R. Grossman,et al.  The time course of evoked depolarization of cortical glial cells. , 1969, Brain research.

[2]  S. Goldring,et al.  Intracellular potentials from "idle" cells in cerebral cortex of cat. , 1966, Electroencephalography and clinical neurophysiology.

[3]  D. E. Goldman POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES , 1943, The Journal of general physiology.

[4]  D. B. Tower,et al.  VARIATION OF CEREBRAL CORTEX FLUID SPACES IN VIVO AS A FUNCTION OF SPECIES BRAIN SIZE. , 1965, The American journal of physiology.

[5]  John L. Walker Ion specific liquid ion exchanger microelectrodes , 1971 .

[6]  L. Rosenhead Conduction of Heat in Solids , 1947, Nature.

[7]  I. Tasaki,et al.  Morphological and physiological properties of neurons and glial cells in tissue culture. , 1962, Journal of neurophysiology.

[8]  D. R. Curtis,et al.  THE EXCITATION OF SPINAL NEURONES BY THE IONOPHORETIC APPLICATION OF AGENTS WHICH CHELATE CALCIUM , 1960, Journal of neurochemistry.

[9]  W. Zieglgänsberger,et al.  Microelectrophoretic studies concerning the spread of glutamic acid and GABA in brain tissue , 2004, Experimental Brain Research.

[10]  J. C. Jaeger,et al.  Conduction of Heat in Solids , 1952 .

[11]  J. Bureš,et al.  The minimum volume of depolarized neural tissue required for triggering cortical spreading depression in rat , 2004, Experimental Brain Research.

[12]  D. Baylor,et al.  After‐effects of nerve impulses on signalling in the central nervous system of the leech , 1969, The Journal of physiology.

[13]  S. W. Kuffler,et al.  GLIA IN THE LEECH CENTRAL NERVOUS SYSTEM: PHYSIOLOGICAL PROPERTIES AND NEURON-GLIA RELATIONSHIP. , 1964, Journal of neurophysiology.

[14]  E Neher,et al.  Measurement of extracellular potassium activity in cat cortex. , 1973, Brain research.

[15]  J. Bureš,et al.  Potassium-selective microelectrodes used for measuring the extracellular brain potassium during spreading depression and anoxic depolarization in rats. , 1972, Brain research.

[16]  A. van Harreveld,et al.  A STUDY OF EXTRACELLULAR SPACE IN CENTRAL NERVOUS TISSUE BY FREEZE-SUBSTITUTION , 1965, The Journal of cell biology.

[17]  E. Neher,et al.  Rapid Changes of Potassium Concentration at the Outer Surface of Exposed Single Neurons during Membrane Current Flow , 1973, The Journal of general physiology.

[18]  P. Dunham,et al.  Diphenylhydantoin (dilantin): stimulation of potassium inflex in lobster axons. , 1971, Brain Research.

[19]  S. W. Kuffler,et al.  Physiological properties of glial cells in the central nervous system of amphibia. , 1966, Journal of neurophysiology.

[20]  G. Sypert,et al.  Unidentified neuroglia potentials during propagated seizures in neocortex. , 1971, Experimental neurology.

[21]  R. Grossman,et al.  Intracellular potentials of inexcitable cells in epileptogenic cortex undergoing fibrillary gliosis after a local injury. , 1971, Brain research.

[22]  E. Ramon‐Moliner,et al.  The histology of the postcruciate gyrus in the cat . I. Quantitative studies , 1961, The Journal of comparative neurology.

[23]  M. Dennis,et al.  Some physiological properties of identified mammalian neuroglial cells , 1969, The Journal of physiology.

[24]  D. Prince Cortical cellular activities during cyclically occurring inter-ictal epileptiform discharges. , 1971, Electroencephalography and clinical neurophysiology.

[25]  A. Hodgkin,et al.  The after‐effects of impulses in the giant nerve fibres of Loligo , 1956, The Journal of physiology.

[26]  D. Pollen,et al.  Neuroglia: Biophysical Properties and Physiologic Function , 1970, Science.

[27]  O J Grüsser,et al.  [Membrane potentials and after dis charges of cortical cells, EEG and cortical DC-potentials in generalized convulsions]. , 1968, Archiv fur Psychiatrie und Nervenkrankheiten.

[28]  J. Buresˇ,et al.  Potassium-selective microelectrodes used for measuring the extracellular brain potassium during spreading depression and anoxic depolarization in rats , 1972 .