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Release probability modulates short‐term plasticity at a rat giant terminal
Author(s) -
Oleskevich Sharon,
Clements John,
Walmsley Bruce
Publication year - 2000
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.2000.00513.x
Subject(s) - excitatory postsynaptic potential , postsynaptic current , neural facilitation , neurotransmission , postsynaptic potential , neuroscience , neurotransmitter , biophysics , chemistry , synapse , stimulation , calcium , synaptic plasticity , pulse (music) , biology , inhibitory postsynaptic potential , central nervous system , physics , biochemistry , receptor , organic chemistry , detector , optics
1 Modulation of release probability is a major factor underlying short‐term synaptic plasticity in the central nervous system. We have investigated the relationship between release probability ( (P r ) and paired‐pulse modulation at a large auditory calyceal synapse containing many transmitter release sites. Whole‐cell patch electrode recordings were made of excitatory postsynaptic currents (EPSCs), evoked by stimulation of auditory nerve fibres giving rise to the endbulbs of Held. 2 Quantitative estimates of P r and quantal amplitude were obtained using the recently developed variance‐mean analysis technique. Release probability conditions were modulated by bath application of cadmium, elevated calcium and protein kinase C activation by phorbol esters. 3 Our results show that, under physiological conditions, most sites released neurotransmitter following a single presynaptic nerve impulse, with a mean P r of 0·6. The mean quantal amplitude was 44 pA, which was consistent with the mean amplitude of miniature EPSCs (47 pA). 4 Under high release probability conditions with elevated calcium or phorbol esters, P r at all sites approached 1·0. At these high P r values, variance‐mean analysis indicated a significant postsynaptic contribution to paired‐pulse depression. The miniature EPSC amplitudes were decreased following stimulation in elevated calcium, confirming a postsynaptic component of paired‐pulse depression at this glutamatergic connection. 5 A notable feature was the large variability between neurons in the relationship between paired‐pulse ratio and P r . Based on current models of vesicle release and ultrastructural evidence, we suggest that this variability may be partly due to morphological differences between endbulb specializations, particularly in the ratio of fusion‐ready to reserve populations of vesicles at endbulb release sites.