TY - JOUR
T1 - Neurotransmitter release
T2 - Facilitation and three-dimensional diffusion of intracellular calcium
AU - Hovav, G.
AU - Parnas, H.
AU - Parnas, I.
PY - 1992/9
Y1 - 1992/9
N2 - In order to account for the time courses of both evoked release and facilitation, in the framework of the Ca2+ hypothesis, Fogelson and Zucker (1985, Biophys. J.48, 1003-1017) suggested treating diffusion of Ca2+, once it enters through the Ca2+ channels, as a three-dimensional process (three-dimensional diffusion model). This model is examined here as a refined version of the "Ca2+-theory" for neurotransmitter release. The three-dimensional model was suggested to account for both the time course of release and that of facilitation. As such, it has been examined here as to its ability to predict the dependence of the amplitude and time course of facilitation under various experimental conditions. It is demonstrated that the three-dimensional diffusion model predicts the time course of facilitation to be insensitive to temperature. It also predicts the amplitude and time course of facilitation to be independent of extracellular Ca2+ concentration. Moreover, it predicts that inhibition of the [Na+]o↔[Ca2+]i exchange does not alter facilitation. These predictions are not upheld by the experimental results. Facilitation is prolonged upon reduction in temperature. The amplitude of facilitation declines and its duration is prolonged upon increase in extracellular Ca2+ concentration. Finally, inhibition of the [Na+]o↔[Ca2+]i exchange prolongs facilitation but does not alter the time course of evoked release after an impulse.
AB - In order to account for the time courses of both evoked release and facilitation, in the framework of the Ca2+ hypothesis, Fogelson and Zucker (1985, Biophys. J.48, 1003-1017) suggested treating diffusion of Ca2+, once it enters through the Ca2+ channels, as a three-dimensional process (three-dimensional diffusion model). This model is examined here as a refined version of the "Ca2+-theory" for neurotransmitter release. The three-dimensional model was suggested to account for both the time course of release and that of facilitation. As such, it has been examined here as to its ability to predict the dependence of the amplitude and time course of facilitation under various experimental conditions. It is demonstrated that the three-dimensional diffusion model predicts the time course of facilitation to be insensitive to temperature. It also predicts the amplitude and time course of facilitation to be independent of extracellular Ca2+ concentration. Moreover, it predicts that inhibition of the [Na+]o↔[Ca2+]i exchange does not alter facilitation. These predictions are not upheld by the experimental results. Facilitation is prolonged upon reduction in temperature. The amplitude of facilitation declines and its duration is prolonged upon increase in extracellular Ca2+ concentration. Finally, inhibition of the [Na+]o↔[Ca2+]i exchange prolongs facilitation but does not alter the time course of evoked release after an impulse.
UR - http://www.scopus.com/inward/record.url?scp=0026917167&partnerID=8YFLogxK
U2 - 10.1007/BF02459934
DO - 10.1007/BF02459934
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 1353391
AN - SCOPUS:0026917167
SN - 0092-8240
VL - 54
SP - 875
EP - 894
JO - Bulletin of Mathematical Biology
JF - Bulletin of Mathematical Biology
IS - 5
ER -