1980
DOI: 10.1002/neu.480110612
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Excitatory neuromuscular transmission in crayfish: Calcium dependence is unaffected by picrotoxin

Abstract: Picrotoxin, 1 X 10(-5)M to 1.6 X 10(-3)M, had little or no effect on the amplitude of intracellularly recorded excitatory junctional potentials (EJPs) at extracellular calcium concentrations [Ca2+]0 ranging from 0.5 to 15 mM. The slope of the log EJP vs. log[Ca2+]0 relationship was approximately 1 with or without picrotoxin. The reduction EJP amplitude resulting from the addition of 5 X 10(-5)M GABA was largely reversed by 10(-5)M picrotoxin.

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Cited by 7 publications
(5 citation statements)
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“…In regard to the second assumption implicit in our model, it has often been reported that the relation between external calcium concentration and transmitter release is linear in crayfish (Bracho and Orkand, 1970;Ortiz and Bracho, 1972;Zucker, 1974;Staggs et al ., 1980), although it has been pointed 36 9 out that saturation of calcium entry could mask a nonlinearity between active calcium and transmitter release (Parnas and Segel, 1981) . Recently, more careful measurements of the relation between transmitter release and external calcium indicate that the relation is nonlinear (Dudel, 1981) and that it is in fact consistent with a fourthor higher-power dependence of transmitter release on intracellular active calcium (Parnas et al ., 1982) .…”
Section: Assumptions and Limitations In Our Modelmentioning
confidence: 99%
“…In regard to the second assumption implicit in our model, it has often been reported that the relation between external calcium concentration and transmitter release is linear in crayfish (Bracho and Orkand, 1970;Ortiz and Bracho, 1972;Zucker, 1974;Staggs et al ., 1980), although it has been pointed 36 9 out that saturation of calcium entry could mask a nonlinearity between active calcium and transmitter release (Parnas and Segel, 1981) . Recently, more careful measurements of the relation between transmitter release and external calcium indicate that the relation is nonlinear (Dudel, 1981) and that it is in fact consistent with a fourthor higher-power dependence of transmitter release on intracellular active calcium (Parnas et al ., 1982) .…”
Section: Assumptions and Limitations In Our Modelmentioning
confidence: 99%
“…This finding was interpreted to contradict the observation of Parnas, Rahamimoff, and Sarne (1975) that picrotoxin, by removing a tonic inhibition, leads to an increase of EPSPs. It is important to note that the latter results were obtained at the neuromuscular junction of a crab (Ocypode), while the findings of Staggs et al (1980) were obtained at crayfish neuromuscular junctions and thus are not seen to "contradict," especially since their conditions were unfavorable for the observation of tonic inhibition. Staggs et al (1980) also emphasized and gave evidence that in crayfish there is a linear dependence of the amplitude of the EPSP on [Ca],, as reported earlier (Bracho and Orkand, 1970;Ortiz and Bracho, 1972;Zucker, 1974).…”
mentioning
confidence: 89%
“…It is important to note that the latter results were obtained at the neuromuscular junction of a crab (Ocypode), while the findings of Staggs et al (1980) were obtained at crayfish neuromuscular junctions and thus are not seen to "contradict," especially since their conditions were unfavorable for the observation of tonic inhibition. Staggs et al (1980) also emphasized and gave evidence that in crayfish there is a linear dependence of the amplitude of the EPSP on [Ca],, as reported earlier (Bracho and Orkand, 1970;Ortiz and Bracho, 1972;Zucker, 1974). Since in vertebrate endplates this dependence is very nonlinear (d log EPSP)I(d log [Calo) = 4 (Dodge and Rahamimoff, 1967), and since this nonlinearity is a prerequisite for explaining the observed facilitation by the residual calcium mechanism, this apparent and "suspect" (Atwood, 1977) deviation of EPSP behavior in crayfish should not be left without comment.…”
mentioning
confidence: 89%
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