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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Reviews on Biomembranes 988 (1989), S. 99-105 
    ISSN: 0304-4157
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 943 (1988), S. 1-12 
    ISSN: 0005-2736
    Keywords: (Frog) ; Arginine residue ; Myelinated nerve fiber ; Potassium current ; Sodium current
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 20 (1964), S. 31-33 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The effect of hypertonic solutions on the action potential of single myelinated nerve fibres is described. Hypertonicity mainly changes the duration of the action potential: Short action potentials obtained in normal Ringer's solution at room temperature are prolonged, long action potentials due to 0.1–1.0 mM NiCl2-Ringer's solution and low temperature are shortened by hypertonicity. The changes in action potential duration are accompanied by small changes in action potential amplitude. In addition, hypertonicity reduces the depolarization produced by 20 mM KCl; inactivation of the sodium-carrying system under cathodal polarization is enhanced.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 19 (1963), S. 377-383 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The recently developed ‘perfused nerve fibre technique’, which consists of perfusing the interior of a squid giant fibre with artificial solutions, is described. The experimental results obtained with various perfusion fluids are discussed in relation to the theory of nerve excitation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Progress in Biophysics and Molecular Biology 33 (1979), S. 207-230 
    ISSN: 0079-6107
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 402 (1984), S. 24-33 
    ISSN: 1432-2013
    Keywords: Myelinated nerve fibre ; Voltage clamp ; Scorpion toxin ; Sea anemone toxin ; KIO3
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 1. In voltage clamped nodes of Ranvier inactivation of the sodium permeability is slowed by toxin V from the scorpionCentruroides sculpturatus, by sea anemone toxin ATX II or by internally applied KIO3. The slow decay of the Na inward current is markedly accelerated if the test pulse is preceded by a depolarizing conditioning pulse followed by a 10–500 ms pause. This phenomenon was studied in detail, using conditioning pulses of varying amplitude and up to 15 s duration. 2. In nodes treated with toxin V a 20 ms conditioning pulse to positive potentials was sufficient to produce a clear acceleration of the decay of the Na current and a reduction of the inward current remaining at the end of a 50 ms test pulse, i.e. a weakening of the toxin effect. In nodes treated with ATX II or internal KIO3 longer conditioning pulses were required. A similar effect of conditioning pulses on the decaying phase of the Na current was also observed in untreated fibres. 3. To study the phenomenon quantitatively we fitted the decaying phase of the inward Na current with the equationI Na=A exp(-t/τ1)+B exp(-t/τ2)+C The effect of depolarizing conditioning pulses could be described as an increase of A, a decrease of B and C and a reduction of the time constants τ1 and τ1. 4. I 50/I peak, the normalised inward current remaining at the end of a 50 ms test pulse, decreased exponentially with increasing duration of the conditioning pulse to a steady-state value. The time constant τ and the steady-state value depended on the potential during the conditioning pulse. For nodes treated with toxin V, τ was 0.24 s at 0 mV and 12° C and half inhibition occurred at −42 mV. The time constant τ was larger for nodes treated with ATX II or internal KIO3. At positive potentials, I50 was reduced to 20% of the control value in toxin V-treated nodes, but only to 70% in KIO3-treated nodes. 5. Recovery from the effect of the conditioning pulse was studied by varying the pause between conditioning pulse and test pulse; recovery was 66–100% complete after 500 ms. 6. The results are interpreted by assuming that a sepolarizing conditioning pulse (a) accelerates inactivation of the sodium permeability and (b) causes dissociation of the toxin-receptor complex or transition into an inactive state. The latter effect occurs in toxin V-treated fibres but not in those treated with ATX II or KIO3.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 407 (1986), S. 18-26 
    ISSN: 1432-2013
    Keywords: Myelinated nerve fibre ; Voltage clamp ; Gating currents ; Chloramine-T
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 1. The experiments were done on voltage-clamped nodes of Ranvier of the frog. The aim was to study the kinetics of sodium currentI Na and gating currentI gat over a large potential range (−92 to −12 mV) and to compare the time constants for the turning-on ofI Na orI gat with those for the turning-off measured at the same potential. 2. Sodium tail currents were recorded at different postpulse potentials. Inactivation was inhibited by a few min treatment with 0.5 mM chloramine-T (Wang 1984). The sodium permeability was activated by a 0.4 ms pulse from holding potential (−92 mV) to about 0 mV. At the peak ofI Na the membrane was repolarized to postpulse potentials between −92 and −12 mV. AtE〉 −60 mV the tail currents decayed with two time constants, τ1 and τ2, reflecting presumably the turning-off and the inactivation of the sodium permeability. The relation between τ1 and postpulse potential was bellshaped with a maximum at −32 mV. 3. The tail currents could also be fitted by the Hodgkin-Huxley equation with the sodium activation variablem raised to the second or third power. AtE〈−50 mV τm off was equal to 2 τ1 or 3 τ1, respectively, whereas atE〉−25 mV τm off was equal to τ1. 4. In addition, the time constant of the turning-on of sodium activationm (τm on) was determined, assumingI Na ∼m 2 (with a small initial delay) orI Na ∼m 3 (without an initial delay). At −22 mV and −12 mV the ratio τm off/τm on was close to 1. At −42 mV and −32 mV it was larger than 1 (1.22 and 1.65 for them 2 andm 3 fit, respectively, at −32 mV). 5. A similar pulse program was used to measure the turning-on and turning-off ofI gat in the presence of 300 nM TTX. In the potential range −52 to −22 mV, no significant difference between τoff and τon (measured at the same potential) was found. This is in conflict with the findings of Dubois and Schneider (1982) who reported an inequality τoff 〈 τon. 6. Comparison between τoff of charge movement and τ1 of the tail current yielded τoff/τ1 = 2.8 at −92 mV. This agrees with previous measurements of Neumcke et al. (1976).
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2013
    Keywords: Myelinated nerve fibre ; Voltage clamp ; Scorpion toxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 1. In nodes of Ranvier treated with toxin III or IV from the scorptionCentruroides sculpturatus Ewing a strong positive pulse is followed by a transient shift of the descending branch of theI Na(E) curve to more negative values of membrane potential (cf. Meves et al. 1982). This effect was studied in more detail, using toxin concentrations between 0.8 and 3.3 μg/ml. 2. The change of theI Na(E) curve was accompanied by a shift of the kinetic parameters of both activation (time to peak, time constant τm) and inactivation (time constant τh1). The τm curve was shifted by the same amount as the descending branch of theI Na(E) curve while the shift of τh1 was somewhat smaller. The curve relating Na permeability to membrane potential became less steep and its lower part was shifted to more negative values of membrane potential. 3. The change of theI Na(E) curve was also accompanied by a change in the turning-on kinetics of the Na current. The normal signoidal time course was replaced by first-order kinetics. A strong hyperpolarizing prepulse restored the sigmoidal time course without abolishing the shift of the descending branch of theI Na(E) curve. 4. The transient change of theI Na(E) curve was not accompanied by a marked change in the ion selectivity of the Na channels: the equilibrium potential decreased only by 4–8 mV. 5. Ca slightly reduced the shift of the descending branch of theI Na(E) curve. The long-lasting inward Na current which follows a strong positive pulse in nodes treated with toxin III or IV was reduced by 7.8 mM Ca to 41% of the value measured in normal *1.8 mM) Ca. Mg was slightly less effective than Ca. 6. From the change of the Na permeability curve the percentage of Na channels transiently modified by a strong positive pulse was estimated as about 50%.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 268 (1958), S. 61-61 
    ISSN: 1432-2013
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 278 (1963), S. 3-3 
    ISSN: 1432-2013
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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