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  • 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: 1432-0568
    Keywords: Muscle precursor cells ; Movement ; Allografts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Regeneration of mature skeletal muscle fibers involves the formation of new multinucleate muscle fibres by the fusion together of mononucleate muscle precursor cells. Such precursor cells appear to be largely or entirely derived from satellite cells, located between the basement membrane and the sarcolemma of the muscle fibre. We have previously presented evidence that precursor cells which contribute to regenerating muscle in a region of muscle damage are not all locally derived but that some migrate in from exogenous sources. The present study examines the possibility that a regenerating muscle might receive muscle precursor cells from neighbouring muscles. To do this we have made whole muscle allografts in the mouse and used the two murine isoenzyme allotypes of the dimeric enzyme Glucose-6-Phosphate Isomerase (GPI) as markers to demonstrate whether there is movement of muscle precursor cells between these allografts and adjacent host muscles. In host muscles adjacent to some allografts, a “hybrid” form of GPI was detected, each molecule consiting of one donor and one host GPI subunit. Such heterodimers can form only where host and donor nuclei share a common cytoplasm: in muscles this means that mosaic host/donor muscle fibres are present. The presence of such fibres implies that muscle precursor cells must have migrated into the host muscle from the neighbouring allograft.
    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
    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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