Abstract
After the arrival of a presynaptic nerve impulse at an excitatory synapse in hippocampal neurons, the rate of neurotransmitter release increases rapidly and then returns to low levels with a biphasic decay. The two kinetically distinct components are differentially affected when Sr2+ is substituted for Ca2+ ions. Our findings are comparable to those of the classical studies for the frog neuromuscular junction, and thus the basic aspects of Ca(2+)-activated transmitter release machinery appear to be conserved in central synapses. The method we have used, in addition, permits us to estimate the average neurotransmitter release rate for a single bouton. The observation of differential Ca2+/Sr2+ sensitivity is consistent with a release mechanism mediated by two Ca2+ sensors with distinct Ca2+ affinities: the low-affinity Ca2+ sensor facilitates the fast synchronous phase of release, whereas the high-affinity sensor sustains the slow asynchronous phase of release.
MeSH Terms
Animals
Calcium/metabolism
Cells, Cultured
Hippocampus/physiology
In Vitro Techniques
Magnesium/metabolism
Mice
Mice, Inbred C57BL
Neurotransmitter Agents/metabolism
Strontium/pharmacology
Synapses/physiology
Synaptic Transmission
Time Factors
Chemicals
Neurotransmitter Agents
Magnesium
Calcium
Strontium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Goda Y
Molecular Neurobiology Laboratory, Salk Institute, La Jolla, CA 92037.
Stevens C F
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