1979
DOI: 10.1016/0306-4522(79)90057-5
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Calcium-dependent release of putative neurotransmitters in the chick visual system

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Cited by 6 publications
(4 citation statements)
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“…We are not able to draw any firm conclusions about the site of EDA uptake, storage or release, as a calcium-dependent release of GABA has been reported from some glial cells (Minchin and Iversen, 1974) and nonsynaptic regions of nerve (Bondy and Harrington, 1979). However, release was evoked in such cases by potassium depolarisation, and we would suggest that the present demonstration of calcium-dependent release of EDA produced by electrical stimulation is more likely to imply neuronal, rather than glial involvement.…”
Section: H G E Lloyd Et Alcontrasting
confidence: 72%
“…We are not able to draw any firm conclusions about the site of EDA uptake, storage or release, as a calcium-dependent release of GABA has been reported from some glial cells (Minchin and Iversen, 1974) and nonsynaptic regions of nerve (Bondy and Harrington, 1979). However, release was evoked in such cases by potassium depolarisation, and we would suggest that the present demonstration of calcium-dependent release of EDA produced by electrical stimulation is more likely to imply neuronal, rather than glial involvement.…”
Section: H G E Lloyd Et Alcontrasting
confidence: 72%
“…Where indicated, aCSF was altered by lowering Ca 2 + and increasing Mg 2 + to either 0.5 mM Ca 2 + /10 mM Mg 2 + (Media-1) or 0.25 mM Ca 2 + /7.25 mM Mg 2 + (Media-2). Flow rates were kept at 2 ml/min to insure adequate infusion of the altered media, consistent with previous published studies (Bondy and Harrington, 1979;Washio and Inouye, 1978;Alderdice and Volle, 1978;Scholfied, 1981). Incubation with such media for 5 min or greater has been shown to block synaptic transmission (Bondy and Harrington, 1979;Washio and Inouye, 1978;Alderdice and Volle, 1978;Scholfied, 1981;Hutter and Kostial, 1954).…”
Section: In Vitro Extracellular Electrophysiologymentioning
confidence: 92%
“…Flow rates were kept at 2 ml/min to insure adequate infusion of the altered media, consistent with previous published studies (Bondy and Harrington, 1979;Washio and Inouye, 1978;Alderdice and Volle, 1978;Scholfied, 1981). Incubation with such media for 5 min or greater has been shown to block synaptic transmission (Bondy and Harrington, 1979;Washio and Inouye, 1978;Alderdice and Volle, 1978;Scholfied, 1981;Hutter and Kostial, 1954). Extracellular electrophysiological recordings were made with glass microelectrodes filled with a solution of 2% pontamine sky-blue in 0.5 M sodium acetate (Yin and French, 2000).…”
Section: In Vitro Extracellular Electrophysiologymentioning
confidence: 92%
“…The importance of GABA as tectal transmitter is demonstrated by biochemical, histochemical, and electrophysiological data. A GABA high-affinity uptake system (Henke et al, 1976~1, muscimol binding sites (Vischer e t al., 19791, and a potassium-stimulated, calcium-dependent, release of GABA in vitro (Reubi and Cuenod, 1976;Bondy and Harrington, 1979) in the tectum have been reported. The activity of tectal neurons is inhibited by iontophoretically applied GABA; this inhibition can be blocked selectively with bicuculline (Barth and Felix, 1974;Felix et al, 1975;Felix, 1982).…”
Section: F Fonnum a N D H Henkementioning
confidence: 95%