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  • 1990-1994  (1)
  • 1980-1984  (2)
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  • 1
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Response properties of single units in the mouse barrel cortex were studied to determine the sequence in which the neurons that form a cortical column become activated by a single‘natural’stimulus. Mice (n= 11) were anaesthetized with urethane. For a total of 153 cells, grouped by cortical layer, responses to a standardized deflection of a single whisker were characterized using poststimulus time and latency histograms. Usually, for each unit, data were collected for stimulation of its principal whisker (PW; the whiskers corresponding to the barrel column in which the cell was located) and of the four whiskers surrounding the PW. In all layers, PW stimulation evoked responses at shorter latency than surround whisker stimulation. In layers II – III and IV a bimodal distribution of cells according to latency to PW stimulation was found. Statistical analysis indicated the presence of two classes of cells in each of these layers:‘fast’units (latency 〈 15 ms) and 'slow’units (latency 〉15 ms). The great majority of cells in layers I, V and VI fired at latencies of 〉20 ms to PW stimulation. In general, stimulation of surround whiskers evoked a smaller response than PW stimulation. The fast cells of layer IV showed the greatest response to PW stimulation (mean = 1.78 spikes/100 ms poststimulus). Their firing was maximal during the 10–20 ms poststimulus epoch, while the slow layer IV cells fired maximally during the 20 – 30 ms poststimulus epoch. Surround inhibition occurred in all layers within the first 10 ms after stimulus onset, during which period the fast cells are the most active ones, and are thus likely to be responsible for the surround inhibition. This notion is supported by an analysis of spike duration that showed that eight of the ten cells with a thin spike (supposed to be GABAergic; McCormick et al., J. Neurophysiol., 54, 782 – 806, 1985), had PW latencies of 〈15 ms. We conclude that the activation of a barrel column is initially inhibitory in nature.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 288 (1980), S. 181-183 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The high-speed polarographic technique was developed from systems being used for evaluating catecholamine levels in the central nervous system9'10. Our system differs principally in that it is some hundreds of times faster, is carried out at the single-cell, rather than macrocellular, level, and ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 39 (1980), S. 327-340 
    ISSN: 1432-1106
    Keywords: Slow waves ; Unitary activity ; Cuneate nucleus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Depth profiles of averaged evoked potentials (AEPs) and simultaneously generated unitary activity have been recorded from the cuneate nucleus of the rat in response to controlled tactile stimulation of the ipsilateral forepaw. Four separate components of the AEPs were isolated, N1, N2, P, and N3. N1corresponds to the classical N wave previously described by other workers; four fractions of N1 are described. The classical P wave which follows N1 reverses at 150–350 μm depth to become a negative wave of identical time course, the N2 wave, at deeper locations. N2 peaks deeper than N1 within the non-relay portion of the cuneate nucleus, or below in the subnuclear reticular førmation where it is the only significant evoked component. Its strong susceptibility to high Mg++ C.S.F. superperfusion suggests a polysynaptic origin. It is argued that the depth distribution and time course of N2 does not support its function relating to depolarisation of primary afferents (PAD) in the vicinity of synaptically driven cuneate cells. Alternative possibilities for its origin are discussed. An additional sustained component of the AEP, the N3 component, is described and evaluated. N3 is co-extensive with N1, has a long time course and simple exponential decay, and is the component most resistant to high Mg++ C.S.F. superperfusion. A similar component to N3 has been described by previous workers in the spinal cord, where it has been shown to arise from glia depolarised by K+ effluxing from discharging afferents and cells. A similar origin for N3 is suggested, and its possible involvement with PAD discussed.
    Type of Medium: Electronic Resource
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