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  • Voltage clamp  (4)
  • Chromatography  (2)
  • (Human)  (1)
  • Aconitine  (1)
  • 1
    ISSN: 0196-9781
    Keywords: Chromatography ; Chromogranin A ; Endocrine cells ; Immunocytochemistry ; Pancreastatin ; Radioimmunoassay
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Regulatory Peptides 27 (1990), S. 307-315 
    ISSN: 0167-0115
    Keywords: Chromatography ; Flanking peptide ; Galanin ; Neuropeptide ; Prohormone ; Radioimmunoassay
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0014-5793
    Keywords: (Human) ; Glucagonoma ; Pancreastatin ; Sequence analysis
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    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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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 409 (1987), S. 381-393 
    ISSN: 1432-2013
    Keywords: Myelinated nerve fibre ; Voltage clamp ; Gating currents ; Scorpion toxins ; Aconitine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract (1) Gating currents were recorded from frog nodes of Ranvier treated either with toxins III or IV from the venom of the scorpionCentruroides sculpturatus or with the alkaloid toxin aconitine. (2) Toxins III or IV fromCentruroides sculpturatus (which drastically reduce the sodium permeabilityP Na and slightly shift its voltage dependence in the depolarizing direction) caused a small depolarizing shift of the relation between charge (Q on) and membrane potential (E) without affecting the maximum chargeQ on max. (3) On nodes treated with toxins III or IV fromCentruroides sculpturatus, a depolarizing conditioning pulse (which transiently shifts the descending branch of theI Na(E) curve by up to 60 mV in the hyperpolarizing direction) shifted the midpoint potential (Emid) of theQ on(E) curve by −17 mV and slightly increased the slope of the curve; it also decreasedQ on max markedly but had little effect onQ on measured with small depolarizing pulses. By contrast, massive treatment with aconitine (which irreversibly shifts sodium activation in the hyperpolarizing direction) irreversibly shifted the midpoint potential of theQ on(E) curve from −28.5 to −69 mV and significantly increasedQ on andQ off measured with small depolarizing pulses; concomitantly, the voltage dependence of the on time constant of the charge movement [τon(E)] was shifted by −44 mV. (4) The sodium currentI Na was exponential both in nodes treated with toxins III or IV ofCentruroides sculpturatus and subjected to a depolarizing conditioning pulse and in aconitine-treated nodes; in the latter,I Na started after a delay of 30–40 μs. The time constant of the sodium current, τon Na, was larger than the time constant of the charge movement, τon Q; the ratio τon Q/τon Na was 0.61 and 0.73 in the experiments withCentruroides sculpturatus toxins and aconitine, respectively. (5) The off time constant of the sodium current (τoff Na) was slightly increased in nodes treated withCentruroides sculpturatus toxins and subjected to a depolarizing conditioning pulse, whereas it was markedly increased in aconitine-treated nodes. With the former treatment, the off time constant of the charge movement (τoff Q) was unaffected but with aconitine treatment it was considerably increased although it remained smaller than τoff Na. Consequently, the ratio τoff Q/τoff Na (which is ≥1 in untreated nodes) became smaller than one, reaching values as low as 0.58 and 0.44 in the experiments withCentruroides sculpturatus toxins and aconitine, respectively. The small τoff Q/τoff Na ratio suggests that the channels remain open for an appreciable time after most of the gating charges have returned to their resting position. (6) The results obtained with aconitine resemble the findings on batrachotoxin-treated nodes (Dubois and Schneider 1985), except that in the latter the time constants τon Na and τoff Na of the sodium current are smaller than the corresponding time constants τon Q and τoff Q of the charge movement.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2013
    Keywords: Myelinated nerve fibre ; Voltage clamp ; Scorpion toxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 1. The effect of various toxin fractions isolated by Watt et al. (1978) from the venom of the scorpionCentruroides sculpturatus Ewing on the Na currents of the node of Ranvier has been studied with the voltage clamp method. 2. The toxin fractions were applied externally. The most potent fractions were toxins III, IV and V which were effective in concentrations of 0.33–3.33 μg/ml. The effect of toxins III and IV was quite different from that of toxin V. 3. In toxin III or IV — treated nodes a strong depolarizing pulse was followed by a transient shift of the negative resistance branch of theI Na (E) curve to more negative potentials. The amount of shift varied between −10 and −60 mV. A 500ms depolarizing pulse of small amplitude produced a slowly developing Na inward current which slowly decayed after the end of the pulse. Inactivation was incomplete, even with 500 ms pulses to 0 mV. 4. The transient shift of theI Na (E) curve was not seen in nodes treated with toxin V. This toxin merely caused slow and incomplete Na inactivation. The effect of toxin IV was not suppressed by a four times higher concentration of toxin V, suggesting that the two toxins act on different receptors. 5. Toxin I acted like toxin IV but was about 10 times less potent. The effect of high concentrations of variants 1, 2, 3, 5, 6 resembled that of toxin V. 6. All effects observed with toxin III or IV were also seen with the whole venom (cf. Cahalan 1975).
    Type of Medium: Electronic Resource
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