Components of field potentials evoked by white matter stimulation in isolated slices of primary visual cortex: spatial distributions and synaptic order.

1. We have recorded profiles of the spatial distributions of extracellular field potentials in transverse slices of rat primary visual cortex. Responses were evoked by electrical stimulation near the white matter/layer VI border and sampled from layers I to V along the radial axis orthogonal to the laminae and intersecting the stimulation site ("on-beam" recording). To assess the activity of "horizontal" connections, we also recorded profiles along axes parallel to the cortical lamination ("off-beam" recording), usually in layer III. Overall, our goal was to extend understanding of the physiology and organization of neocortical circuitry and to provide a basis for comparisons of data from different experiments and experimenters when neocortical field potentials are used in studies of plasticity and pharmacology. 2. Responses were highly specific with respect to the cortical layers. We distinguish four major components: two kinds of population spike ("S1" and "S2") and two slower waveforms ("W1" and "W2"). The latter appear to represent flow of current in apical dendrites of the supragranular layers. Component W1, the earliest slow component, is a synaptically driven field potential dipole that is positive in layer I and negative in layer II. Based on estimates of current source densities (CSDs), we attribute this to entry of depolarizing current into dendrites and/or cell somata in layer II, ascending intradendritic current, and passive depolarization of inactive dendritic membrane in layer I. Component W1 rises during the 20 ms after stimulation and falls during the 50-100 ms thereafter. Component W2 is also positive in layer I but maximally negative in layer III. It rises for approximately 100 ms after stimulation and decays during the following 400-800 ms. 3. Component S1 does not depend on synaptic transmission because it persists during the application of glutamate receptor antagonists or medium that is low in Ca2+. This component is largest in layer III, radial to the site of stimulation. There, it is a negative deflection, typically 1-2 mV in amplitude and lasting roughly 2 ms, with a latency to peak between 2 and 4.5 ms. Component S1 is most likely a population spike due to synchronized firing of cell somata activated antidromically via unmyelinated efferent axons. 4. Component S2 is a short (less than 20 ms) burst of population spikes specifically in layer III. Individual S2 spikes closely resemble S1 spikes, and we propose that the same neuronal population generates both. However, S2 spikes require glutamatergic synaptic transmission.(ABSTRACT TRUNCATED AT 400 WORDS)

[1]  P. Andersen,et al.  Functional characteristics of unmyelinated fibres in the hippocampal cortex , 1978, Brain Research.

[2]  E. Harth,et al.  A Computerized Study of Golgi-Impregnated Axons in Rat Visual Cortex , 1977 .

[3]  N Yamamoto,et al.  Neural connections between the lateral geniculate nucleus and visual cortex in vitro. , 1989, Science.

[4]  D R Humphrey,et al.  Re-analysis of the antidromic cortical response. II. On the contribution of cell discharge and PSPs to the evoked potentials. , 1968, Electroencephalography and clinical neurophysiology.

[5]  B. Connors,et al.  Horizontal spread of synchronized activity in neocortex and its control by GABA-mediated inhibition. , 1989, Journal of neurophysiology.

[6]  Karl J. Zilles,et al.  The Cortex of the Rat: A Stereotaxic Atlas , 1985 .

[7]  G. Shepherd,et al.  Theoretical reconstruction of field potentials and dendrodendritic synaptic interactions in olfactory bulb. , 1968, Journal of neurophysiology.

[8]  T. Teyler,et al.  The neural circuitry of the neocortex examined in the in vitro brain slice preparation , 1982, Brain Research.

[9]  H. Swadlow,et al.  Efferent systems of the rabbit visual cortex: Laminar distribution of the cells of origin, axonal conduction velocities, and identification of axonal branches , 1981, The Journal of comparative neurology.

[10]  J. Schmidt,et al.  Effect of α-bungarotoxin on retinotectal synaptic transmission in the goldfish and the toad , 1980, Neuroscience.

[11]  B. Connors,et al.  Electrophysiological properties of neocortical neurons in vitro. , 1982, Journal of neurophysiology.

[12]  K. Toyama,et al.  Electrophysiological study of synaptic connections between a transplanted lateral geniculate nucleus and the visual cortex of the host rat , 1987, Brain Research.

[13]  M. Gutnick,et al.  Dye coupling and possible electrotonic coupling in the guinea pig neocortical slice. , 1981, Science.

[14]  B W Connors,et al.  Synchronized excitation and inhibition driven by intrinsically bursting neurons in neocortex. , 1989, Journal of neurophysiology.

[15]  P. Andersen,et al.  A comparison of distal and proximal dendritic synapses on CA1 pyramids in guinea‐pig hippocampal slices in vitro , 1980, The Journal of physiology.

[16]  W. Singer,et al.  Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties , 1989, Nature.

[17]  D. McCormick,et al.  Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex. , 1985, Journal of neurophysiology.

[18]  W Singer,et al.  Monocular activation of visual cortex in normal and monocularly deprived cats: an analysis of evoked potentials. , 1980, The Journal of physiology.

[19]  W. Singer,et al.  Long-term potentiation and NMDA receptors in rat visual cortex , 1987, Nature.

[20]  U. Mitzdorf Current source-density method and application in cat cerebral cortex: investigation of evoked potentials and EEG phenomena. , 1985, Physiological reviews.

[21]  T. Tsumoto,et al.  Long‐term potentiation and N‐methyl‐D‐aspartate receptors in the visual cortex of young rats. , 1989, The Journal of physiology.

[22]  Y. Kang,et al.  Excitatory synaptic actions between pairs of neighboring pyramidal tract cells in the motor cortex. , 1988, Journal of neurophysiology.

[23]  J. Hablitz,et al.  EPSPs in rat neocortical neurons in vitro. I. Electrophysiological evidence for two distinct EPSPs. , 1989, Journal of neurophysiology.

[24]  Alan Peters,et al.  Cellular components of the cerebral cortex , 1984 .

[25]  K Toyama,et al.  Long-term potentiation of synaptic transmission in kitten visual cortex. , 1988, Journal of neurophysiology.

[26]  G. Henry,et al.  Ordinal position of neurons in cat striate cortex. , 1979, Journal of neurophysiology.

[27]  G. Shepherd,et al.  Current-density analysis of summed evoked potentials in opossum prepyriform cortex. , 1973, Journal of neurophysiology.

[28]  R. B. Langdon,et al.  Pharmacology of retinotectal transmission in the goldfish: effects of nicotinic ligands, strychnine, and kynurenic acid , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  R Llinás,et al.  The action of antidromic impulses on the cerebellar Purkinje cells , 1966, The Journal of physiology.

[30]  R S Jacobs,et al.  An inexpensive frequency-modulated (FM) audio monitor of time-dependent analog parameters. , 1980, Journal of pharmacological methods.

[31]  A. Schleicher,et al.  The monocular and binocular subfields of the rat's primary visual cortex: A quantitative morphological approach , 1984, The Journal of comparative neurology.

[32]  Hsiang-Tung Chang,et al.  An analysis of primary response of visual cortex to optic nerve stimulation in cats. , 1950, Journal of neurophysiology.

[33]  R. Miles,et al.  Excitatory synaptic interactions between CA3 neurones in the guinea‐pig hippocampus. , 1986, The Journal of physiology.

[34]  C. Gilbert Microcircuitry of the visual cortex. , 1983, Annual review of neuroscience.

[35]  B. Connors,et al.  Periodicity and directionality in the propagation of epileptiform discharges across neocortex. , 1988, Journal of neurophysiology.

[36]  A. Burkhalter,et al.  Intrinsic connections of rat primary visual cortex: Laminar organization of axonal projections , 1989, The Journal of comparative neurology.

[37]  L. Swanson The Rat Brain in Stereotaxic Coordinates, George Paxinos, Charles Watson (Eds.). Academic Press, San Diego, CA (1982), vii + 153, $35.00, ISBN: 0 125 47620 5 , 1984 .

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

[39]  T. Teyler,et al.  A critical period for long-term potentiation in the developing rat visual cortex , 1988, Brain Research.

[40]  W. Rall Time constants and electrotonic length of membrane cylinders and neurons. , 1969, Biophysical journal.

[41]  J. T. Hackett Calcium dependency of excitatory chemical synaptic transmission in the frog cerebellum in vitro , 1976, Brain Research.

[42]  A. Thomson,et al.  Voltage-dependent currents prolong single-axon postsynaptic potentials in layer III pyramidal neurons in rat neocortical slices. , 1988, Journal of neurophysiology.

[43]  R. B. Langdon,et al.  Goldfish retinotectal transmission in vitro: component current sink-source pairs isolated by varying calcium and magnesium levels , 1988, Brain Research.

[44]  C. Nicholson,et al.  Theory of current source-density analysis and determination of conductivity tensor for anuran cerebellum. , 1975, Journal of neurophysiology.

[45]  R. Llinás,et al.  Antidromic invasion of Purkinje cells in frog cerebellum. , 1969, Journal of neurophysiology.

[46]  G. Somjen,et al.  Calcium dependance of synaptic transmission in the hippocampal slice , 1981, Brain Research.

[47]  R. Traub,et al.  Model of the origin of rhythmic population oscillations in the hippocampal slice. , 1989, Science.

[48]  L. Kruger,et al.  Multiple responses and excitability of cat's visual cortex. , 1956, Journal of neurophysiology.

[49]  Y. Frégnac,et al.  Development of neuronal selectivity in primary visual cortex of cat. , 1984, Physiological reviews.

[50]  S. Levay,et al.  Patchy intrinsic projections in visual cortex, area 18, of the cat: Morphological and immunocytochemical evidence for an excitatory function , 1988, The Journal of comparative neurology.

[51]  W. Singer,et al.  Stimulus-specific neuronal oscillations in orientation columns of cat visual cortex. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[52]  R. L. Nó,et al.  Action potential of the motoneurons of the hypoglossus nucleus. , 1947 .

[53]  Kevin S. Lee Sustained enhancement of evoked potentials following brief, high-frequency stimulation of the cerebral cortex in vitro , 1982, Brain Research.

[54]  A. Peters,et al.  The neuronal composition of area 17 of rat visual cortex. I. The pyramidal cells , 1985, The Journal of comparative neurology.

[55]  D. Hubel Evolution of ideas on the primary visual cortex, 1955–1978: A biased historical account , 1982, Bioscience reports.

[56]  W Rall,et al.  Computed potentials of cortically arranged populations of neurons. , 1977, Journal of neurophysiology.

[57]  S. W. Kuffler,et al.  NATURE OF THE "ENDPLATE POTENTIAL" IN CURARIZED MUSCLE , 1941 .

[58]  J. Taube,et al.  Mechanisms of long-term potentiation: a current-source density analysis , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[59]  C. D. Richards,et al.  Calcium, magnesium and the electrical activity of guinea‐pig olfactory cortex in vitro , 1970, The Journal of physiology.

[60]  J G Parnavelas,et al.  Organization of neurons in the visual cortex, area 17, of the rat. , 1977, Journal of anatomy.

[61]  B. Connors Initiation of synchronized neuronal bursting in neocortex , 1984, Nature.

[62]  S. Sherman,et al.  Organization of visual pathways in normal and visually deprived cats. , 1982, Physiological reviews.

[63]  F. Edward Dudek,et al.  Local synaptic circuits in rat hippocampus: interactions between pyramidal cells , 1980, Brain Research.

[64]  R. Llinás,et al.  Field potentials in the alligator cerebellum and theory of their relationship to Purkinje cell dendritic spikes. , 1971, Journal of neurophysiology.

[65]  D. Whitteridge,et al.  Form, function and intracortical projections of spiny neurones in the striate visual cortex of the cat. , 1984, The Journal of physiology.