Ion and transmitter movements during spreading cortical depression.

A reaction--diffusion system of equations whose components are the extracellular concentrations of K+, Ca++, Na+, Cl-, an excitatory neurotransmitter and an inhibitory neurotransmitter, is developed in order to model the movements of these substances through various kinds of membrane in brain structures. Expressions are derived from probabilistic arguments for the conductances induced in subsynaptic membrane by transmitter substances at various concentrations, for one-way active transport rates and for an exchange pump rate. These expressions are employed in the reaction terms of the system. The meaning of the many constants is explained and, with appropriate choices for their values, the model predicts subthreshold responses to small enough local elevations of KCl or glutamate and stable propagating SD waves if the local elevations of these chemicals is sufficient. The SD waves consist of elevated K+ and transmitter substances and diminished Ca++, Na+ and Cl-, the velocity of propagation in cortex being about 0.6 mm/min. This is in the experimental range, the K+-amplitude being 17 mM relative to a baseline of 3 mM, as the model developed ignores the effects of action potentials. There is no SD response to either NaCl or GABA. The effects of no K+ and no glutamate diffusion are investigated, both being manifest as a failure in propagation of the stable SD waves. The wave solutions are analysed in terms of phase portraits. The roles of various amino acid uptake and release processes by neurons and glia are discussed, as are the complications with regard to their incorporation in a model for SD. The roles of neurons and glia are analysed and the six basic fluxes of K+ are outlined. It is postulated that under some circumstances, in cortex treated with TTX, there may be practically no transmitter release, but SD may propagate if TTX does not completely abolish gNa for nonsynaptic membrane, a corresponding system of model equations being developed. The data and ideas of K+-based and glutamate-based SD of Van Harreveld are discussed and interpreted in terms of which reaction terms are operative in the K+ equation. An appendix contains the values of the parameters used in the numerical calculations.

[1]  R. Hollingsworth,et al.  A model of GABA transport by cortical synaptosomes from the long‐evans rat , 1979, Journal of neuroscience research.

[2]  B. Grafstein,et al.  Mechanism of spreading cortical depression. , 1956, Journal of neurophysiology.

[3]  A. van Harreveld,et al.  Glutamate release from the retina during spreading depression. , 1970, Journal of neurobiology.

[4]  A. van Harreveld,et al.  Glutamate and spreading depression. , 1974, Journal of Neurobiology.

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

[6]  L. Potter Synthesis, storage and release of [14C]acetylcholine in isolated rat diaphragm muscles , 1970, The Journal of physiology.

[7]  A. R. Gardner-Medwin,et al.  Diffusion from an iontophoretic point source in the brain: role of tortuosity and volume fraction , 1979, Brain Research.

[8]  J. Bureš SOME METABOLIC ASPECTS OF LEÃO'S SPREADING DEPRESSION , 1956, Journal of neurochemistry.

[9]  E. Kandel,et al.  Potassium outflux from rabbit cortex during spreading depression. , 1960, Journal of neurophysiology.

[10]  J. Blankenship Action of tetrodotoxin on spinal motoneurons of the cat. , 1968, Journal of neurophysiology.

[11]  C. Nicholson,et al.  Calcium and potassium changes in extracellular microenvironment of cat cerebellar cortex. , 1978, Journal of neurophysiology.

[12]  J. H. Schwartz,et al.  Metabolism of acetylcholine in the nervous system of Aplysia californica. IV. Studies of an identified cholinergic axon , 1977, The Journal of general physiology.

[13]  W. H. Miller,et al.  Müller cell function during spreading depression in frog retina. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[14]  C. Nicholson,et al.  Anion permeability in spreading depression investigated with ion-sensitive microelectrodes , 1979, Brain Research.

[15]  R. Llinás,et al.  Presynaptic calcium currents in squid giant synapse. , 1981, Biophysical journal.

[16]  C. Nicholson,et al.  Extracellular ionic variations during spreading depression , 1978, Neuroscience.

[17]  D. Fambrough Acetylcholine receptors. Revised estimates of extrajunctional receptor density in denervated rat diaphragm. , 1974 .

[18]  C. Nicholson,et al.  Chloride and potassium changes measured during spreading depression in catfish cerebellum , 1975, Brain Research.

[19]  A. Harreveld Two mechanisms for spreading depression in the chicken retina , 1978 .

[20]  A. A. Leão,et al.  SPREADING DEPRESSION OF ACTIVITY IN THE CEREBRAL CORTEX , 1944 .

[21]  H C Tuckwell,et al.  A mathematical model for spreading cortical depression. , 1978, Biophysical journal.

[22]  S. Ochs The Nature of Spreading Depression in Neural Networks , 1962 .

[23]  R. J. Carmo,et al.  On the relation of glutamic acid and some allied compounds to corticl spreading depression. , 1972, Brain research.

[24]  W. Zieglgänsberger,et al.  Tetrodotoxin interference of CNS excitation by glutamic acid. , 1972, Nature: New biology.

[25]  A. Hamberger,et al.  Potassium-stimulated γ-aminobutyric acid release from neurons and glia , 1977, Brain Research.

[26]  S. Ochs,et al.  Spreading depression of negative wave of direct cortical response and pyramidal tract responses. , 1970, Brain research.

[27]  Potassium-stimulated gamma-aminobutyric acid release from neurons and glia. , 1977, Brain research.

[28]  E Sugaya,et al.  Neuronal and glial activity during spreading depression in cerebral cortex of cat. , 1975, Journal of neurophysiology.

[29]  D. L. Martin,et al.  SODIUM‐DEPENDENT EFFLUX AND EXCHANGE OF GABA IN SYNAPTOSOMES , 1974, Journal of neurochemistry.

[30]  C. Campbell The Na+, K+, Cl− contents and derived membrane potentials of presynaptic nerve endings in vitro , 1976, Brain Research.

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

[32]  P. Gage,et al.  Dual Effect of Potassium on Transmitter Release , 1965, Nature.

[33]  K. Krnjević,et al.  Evidence for Ca2+-activated K+ conductance in cat spinal motoneurons from intracellular EGTA injections. , 1975, Canadian journal of physiology and pharmacology.

[34]  K. Krnjević,et al.  Chemical Nature of Synaptic Transmission in Vertebrates , 1974 .

[35]  R. Hollingsworth,et al.  A MODEL OF HIGH AFFINITY GLUTAMIC ACID TRANSPORT BY CORTICAL SYNAPTOSOMES FROM THE LONG‐EVANS RAT , 1978, Journal of neurochemistry.

[36]  H. Tuckwell Solitons in a Reaction-Diffusion System , 1979, Science.

[37]  O. Burešová,et al.  The mechanism and applications of Leão's spreading depression of electroencephalographic activity , 1974 .

[38]  A. Hodgkin,et al.  A quantitative description of membrane current and its application to conduction and excitation in nerve , 1952, The Journal of physiology.

[39]  A. Harreveld COMPOUNDS IN BRAIN EXTRACTS CAUSING SPREADING DEPRESSION OF CEREBRAL CORTICAL ACTIVITY AND CONTRACTION OF CRUSTACEAN MUSCLE , 1959 .

[40]  H. Tuckwell Evidence of Soliton-Like Behavior of Solitary Waves in a Nonlinear Reaction-Diffusion System , 1980 .

[41]  J. Schadé,et al.  Chloride movements in cerebral cortex after circulatory arrest and during spreading depression. , 1959, Journal of cellular and comparative physiology.

[42]  C. Nicholson,et al.  Sodium liquid ion exchanger microelectrode used to measure large extracellular sodium transients. , 1976, Science.

[43]  A. Vanharreveld,et al.  Ion and water movements in isolated chicken retinas during spreading depression. , 1972 .

[44]  T. Rasmussen,et al.  Amino acid content of epileptogenic human brain: focal versus surrounding regions. , 1972, Brain research.

[45]  V. P. Whittaker The application of subcellular fractionation techniques to the study of brain function. , 1988, Progress in biophysics and molecular biology.

[46]  K. Krnjević,et al.  Intracellular Mg2+ increases neuronal excitability. , 1976, Canadian journal of physiology and pharmacology.

[47]  A. van Harreveld Two mechanisms for spreading depression in the chicken retina. , 1978, Journal of neurobiology.

[48]  H. Grundfest,et al.  The Action of Tetrodotoxin on Electrogenic Components of Squid Giant Axons , 1965, The Journal of General Physiology.

[49]  A. Hodgkin,et al.  The effect of temperature on the electrical activity of the giant axon of the squid , 1949, The Journal of physiology.

[50]  An Extrapolated Crank-Nicolson Difference Scheme for Quasilinear Parabolic Equations† , 1967 .

[51]  B Katz,et al.  The binding of acetylcholine to receptors and its removal from the synaptic cleft , 1973, The Journal of physiology.

[52]  R. Llinás,et al.  Tetrodotoxin-resistant dendritic spikes in avian Purkinje cells. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[53]  C. Nicholson,et al.  Calcium modulation in brain extracellular microenvironment demonstrated with ion-selective micropipette. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[54]  A. van Harreveld Compounds in brain extracts causing spreading depression of cerebral cortical activity and contraction of crustacean muscle. , 1959, Journal of neurochemistry.

[55]  J. H. Quastel,et al.  FATE OF l‐GLUTAMATE IN THE BRAIN , 1974, Journal of neurochemistry.

[56]  F. Orrego Criteria for the identification of central neurotransmitters, and their application to studies with some nerve tissue preparations in vitro , 1979, Neuroscience.

[57]  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.

[58]  J. H. Schwartz,et al.  Synaptic release of radioactivity after intrasomatic injection of choline-3H into an identified cholinergic interneuron in abdominal ganglion of Aplysia californica. , 1974, Journal of neurophysiology.

[59]  W. H. Marshall,et al.  Spreading cortical depression of Leao. , 1959, Physiological reviews.

[60]  G. Fagg,et al.  The uptake and release of putative amino acid neurotransmitters , 1979, Neuroscience.

[61]  F. Fonnum,et al.  The concentration of GABA within inhibitory nerve terminals. , 1973, Brain research.

[62]  D. D. Wheeler,et al.  Effects of polarizing currents and repetitive stimulation on the uptake of amino acids by peripheral nerve , 1979, Journal of neuroscience research.

[63]  B. Katz,et al.  A study of the ‘desensitization’ produced by acetylcholine at the motor end‐plate , 1957, The Journal of physiology.

[64]  P. Roberts,et al.  [14C]GLUTAMATE UPTAKE AND COMPARTMENTATION IN GLIA OF RAT DORSAL SENSORY GANGLION , 1974, Journal of neurochemistry.

[65]  H C Tuckwell,et al.  Predictions and properties of a model of potassium and calcium ion movements during spreading cortical depression. , 1980, The International journal of neuroscience.

[66]  S. Snyder,et al.  Potassium-induced release of amino acids from cerebral cortex and spinal cord slices of the rat. , 1974, Brain research.

[67]  J. H. Schwartz,et al.  Metabolism of acetylcholine in the nervous system of Aplysia californica. III. Studies of an indentified cholinergic neuron , 1975, The Journal of general physiology.

[68]  C. Cotman,et al.  Evaluation of glutamate as a neurotransmitter of cerebellar parallel fibers , 1978, Neuroscience.