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  • 1
    ISSN: 1432-2013
    Keywords: Crayfish neuromuscular junction ; Veratridine ; Inhibitory synapse ; Spontaneous quantal release ; Extracellular calcium ; Noise analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Crayfish fibres of opener muscles were voltage clamped toE=−80 mV membrane potential (T=19–22°C), and veratridine (10–100 μmol/l) was added to the superfusate. Within 30–60 s this caused large fluctuations of the clamp current due to vigorous asynchronous quantal release from the inhibitory nerve terminals along the muscle fibre. Excitatory postsynaptic receptors were previously desensitized by application of 5 mmol/l glutamate. Current fluctuations were evaluated by means of the noise analysis technique. Typically, 100 μmol/l veratridine increased instantaneously the quantal release rate ñ from ñ〈1 quantum/s toñ≃10,000 quanta/s. Thereafter, ñ declined exponentially with a time constant of ≃ 70s. On average, about 500,000 inhibitory quanta could be liberated in this way from the terminals on a single muscle fibre of ≃ 1 mm length. Serotonin (1 μmol/l) facilitated the effect of lower veratridine concentrations (1–10 μmol/l). In opener muscles veratridine-induced asynchronous quantal release showed little dependence on the bath concentration of Ca2+. The opposite was found for fibres of the superficial abdominal extensor muscle. Beside postsynaptic current fluctuations, veratridine elicited slowly changing average postsynaptic DC-currents which could be explained partly by superposition of individual inhibitory quantal currents. These DC-currents suggest that beside inhibitory quantal release another factor activates inhibitory postsynaptic receptors after application of veratridine.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Inhibitory synapse ; Veratridine ; Lithium ; Quantal release ; Non-quantal release ; Noise analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Muscle fibres of small crayfish were voltage clamped and superfused for about 10 min with Li+ saline (Na+ replaced by Li+) which contained 5 mmol/l glutamate to desensitize excitatory postsynaptic receptors. Then 100 μmol/l veratridine were added to the superfusate which caused strong asynchronous quantal release of inhibitory transmitter. However, in the presence of Li+ strong inhibitory quantal release was only transient. It could be activated a second time by removal of Li+ and readministration of Na+. From the total of 0.7 to 1.1 million quanta released by veratridine only about 30–35% could be released in Li+ saline. The voltage clamp DC-currents recorded during veratridine-induced quantal release suggested that a nonquantal release component is additionally involved. This non-quantal release component was most prominent during the period of quantal release in Li+ superfusate while it was less obvious during the second enhancement of quantal release in normal saline. Together with previous results (Martin and Finger 1988) it may be concluded that quantal release, but not non-quantal release, is decreased by Li+ in the nerve terminals.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2013
    Keywords: Crayfish neuromuscular junction ; Veratridine ; Excitatory synapse ; Asynchronous quantal release ; Quantal store of transmitter ; Calcium ; Noise analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract At single voltage-clamped opener muscle fibres of crayfish claw, 10–100 μmol/l veratridine increased within a few seconds the rate of asynchronous quantal release, ñ, of excitatory transmitter from ñ〈1 quantum/s to ñ≃10,000 quanta/s. Thereafter ñ declined exponentially either with a single, τ(2)≃50 s, or with two time constants τ(1)≃19 s, τ(2)≃50 s. In total (t→∞), about 0.3 million quanta were released by veratridine in a single short fibre of about 1 mm length. These values were estimated by means of the noise analysis technique and they agreed with equivalent parameters of release when 100 mmol/l K+ were used as release stimulus. Strong quantal release could be elicited only once in a single muscle by veratridine. Furthermore, the effect of veratridine on quantal release could be completely prevented by pretreatment with tetrodotoxin. In another nerve-muscle preparation of crayfish, the abdominal superficial extensor muscle, up to 3 million excitatory quanta could be released by veratridine in a single fibre. In the latter muscle veratridine-induced asynchronous quantal release was strongly dependent on the extracellular concentration of Ca2+ whereas in the claw opener dependence of quantal release on extracellular Ca2+ was negligible.
    Type of Medium: Electronic Resource
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