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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 20 (1991), S. 165-176 
    ISSN: 1432-1017
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Using a very low noise voltage clamp technique it has been possible to record from the squid giant axon a slow component of gating current (I g ) during the inactivation phase of the macroscopic sodium current (I Na ) which was hitherto buried in the baseline noise. In order to examine whether this slowI g contains gating charge that originates from transitions between the open (O) and the inactivated (I) states, which would indicate a true voltage dependence of inactivation, or whether other transitions contribute charge to slowI g , a new model independent analysis termed isochronic plot analysis has been developed. From a direct correlation ofI g and the time derivative of the sodium conductance dg Na/d the condition when only O-I transitions occur is detected. Then the ratio of the two signals is constant and a straight line appears in an isochronic plot ofI g vs. dg Na/d . Its slope does not depend on voltage or time and corresponds to the quantal gating charge of the O-I transition (q h ) divided by the single channel ionic conductance (γ). This condition was found at voltages above − 10 mV up to + 40 mV and a figure of 1.21e − was obtained forq h at temperatures of 5 and 15°C. At lower voltages additional charge from other transitions, e.g. closed to open, is displaced during macroscopic inactivation. This means that conventional Eyring rate analysis of the inactivation time constant τ h is only valid above − 10 mV and here the figure forq h was confirmed also from this analysis. It is further shown that most of the present controversies surrounding the voltage dependence of inactivation can be clarified. The validity of the isochronic plot analysis has been confirmed using simulated gating and ionic currents.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurocytology 17 (1988), S. 145-159 
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In order to investigate the transglial pathways in the Schwann sheath of squid giant axons, an electron microscopic study of thin sections and freeze-fracture replicas was carried out. Hitherto the mesaxonal clefts between Schwann cells were regarded as the only pathway between the extracellular space and the periaxonal space which, like the clefts, is about 10 nm in width. The clefts were now found to be obstructed by a putative single-stranded tight junction between neighbouring Schwann cells along the entire border near the axon. The Schwann cells were found to be penetrated like a sponge by a three-dimensional tubular transglial lattice that is confluent with the periaxonal space, the mesaxonal clefts and the extracellular space. The transglial channel system (TGCS) would, therefore, serve as an alternative diffusional pathway, provided that the tubular lumen was permeable. The diameter of the tubules is about 40 nm. In freeze-fracture replicas the density of tubular openings towards the axon was estimated to be 3.3 ± 0.72 per µm2. In relation to the periaxonal cell surface, this constitutes a relative opening area of 0.42% as compared to the 0.15% of the mesaxonal clefts (neglecting their tight junctions). Therefore, the TGCS would provide a ubiquitous access for ionic flow between axolemma and extracellular space. The fact that the TGCS has only recently been observed in squid, but has been described for some time in the giant nerve fibres of crayfish and lobster, can be explained by the use of different fixation methods. The TGCS system is preserved in aldehyde fixation as used in the present study, whereas osmium tetroxide was applied in earlier work on squid. The comparison with the results obtained in other species suggests strongly that the TGCS is permeable and constitutes a transglial pathway for rapid ionic flow.
    Type of Medium: Electronic Resource
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