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Articles

A role for postsynaptic neurons in determining presynaptic release properties in the cricket CNS: evidence for retrograde control of facilitation

GW Davis and RK Murphey
Journal of Neuroscience 1 September 1993, 13 (9) 3827-3838; DOI: https://doi.org/10.1523/JNEUROSCI.13-09-03827.1993
GW Davis
Neuroscience and Behavior Program, University of Massachusetts, Amherst 01003.
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RK Murphey
Neuroscience and Behavior Program, University of Massachusetts, Amherst 01003.
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Abstract

Intracellular recording sin the cricket cercal system show that the synaptic terminals of a single sensory neuron can facilitate at one target, the medial giant interneuron (MGI), and simultaneously depress at another target, interneuron 10–3. A quantal analysis of transmission at these synapses demonstrates that facilitation and depression are properties of the presynaptic cell. For facilitating synapses contacting MGI, the mean quantal content (m), determined from the probability of the failures, increases for the second EPSP, while the quantal size (q) remains constant. Similarly, an analysis of depression for those synapses contacting 10–3 supports a presynaptic mechanism for depression. Since facilitation and depression are presynaptic and their expression at the synapses of a single, identified sensory neuron are correlated with the target interneuron, we conclude that these properties are regulated locally, at the synapse, possibly by an interaction with the postsynaptic cell.

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The Journal of Neuroscience: 13 (9)
Journal of Neuroscience
Vol. 13, Issue 9
1 Sep 1993
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A role for postsynaptic neurons in determining presynaptic release properties in the cricket CNS: evidence for retrograde control of facilitation
GW Davis, RK Murphey
Journal of Neuroscience 1 September 1993, 13 (9) 3827-3838; DOI: 10.1523/JNEUROSCI.13-09-03827.1993

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A role for postsynaptic neurons in determining presynaptic release properties in the cricket CNS: evidence for retrograde control of facilitation
GW Davis, RK Murphey
Journal of Neuroscience 1 September 1993, 13 (9) 3827-3838; DOI: 10.1523/JNEUROSCI.13-09-03827.1993
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