Abstract
An important issue in synaptic physiology is the extent to which postsynaptic receptors are saturated by the neurotransmitter released from a single synaptic vesicle. Although the bulk of evidence supports receptor saturation, recent studies have started to reveal that alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and N-methyl-D-aspartate (NMDA) receptors may not be saturated by a single vesicle of glutamate. Here, we address this question through a study of putative single synapses, made by hippocampal neurons in culture, that are identified by FM1-43 staining. An analysis of the sources of variability in the amplitudes of miniature excitatory postsynaptic currents at single synapses reveals that this variability must arise presynaptically, from variations in the quantity of agonist released. Thus, glutamate receptors at hippocampal synapses are not generally saturated by quantal release.
MeSH Terms
6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology
Animals
Binding, Competitive
Cells, Cultured
Dizocilpine Maleate/pharmacology
Dose-Response Relationship, Drug
Excitatory Amino Acid Agonists/pharmacology
Excitatory Amino Acid Antagonists/pharmacology
Glutamic Acid/pharmacology
Iontophoresis
N-Methylaspartate/pharmacology
Patch-Clamp Techniques
Pyramidal Cells/drug effects,metabolism
Rats
Receptors, AMPA/drug effects,metabolism
Receptors, N-Methyl-D-Aspartate/drug effects,metabolism
Synapses/metabolism
Synaptic Transmission
Chemicals
Excitatory Amino Acid Agonists
Excitatory Amino Acid Antagonists
Receptors, AMPA
Receptors, N-Methyl-D-Aspartate
Glutamic Acid
N-Methylaspartate
Dizocilpine Maleate
6-Cyano-7-nitroquinoxaline-2,3-dione
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
McAllister A K
Howard Hughes Medical Institute, The Salk Institute, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
[email protected]
Stevens C F
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