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Specific-opiate-induced depression of transmitter release from dorsal root ganglion cells in culture.

Specific-opiate-induced depression of transmitter release from dorsal root ganglion cells in... The opiate etorphine depresses monosynaptic excitatory postsynaptic potentials (EPSP's) elicited in spinal cord cells by activation of dorsal root ganglion cells in murine neuronal cell culture. The depression is reversed by naloxone. Statistical analysis of the synaptic responses reveals that the opiate reduces EPSP quantal content at this synapse without altering quantal size. Therefore, the opiate action is presynaptic and affects transmitter release rather than postsynaptic responsiveness. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Science (New York, N.Y.) Pubmed

Specific-opiate-induced depression of transmitter release from dorsal root ganglion cells in culture.

Science (New York, N.Y.) , Volume 199 (4336): -1397 – Apr 26, 1978

Specific-opiate-induced depression of transmitter release from dorsal root ganglion cells in culture.


Abstract

The opiate etorphine depresses monosynaptic excitatory postsynaptic potentials (EPSP's) elicited in spinal cord cells by activation of dorsal root ganglion cells in murine neuronal cell culture. The depression is reversed by naloxone. Statistical analysis of the synaptic responses reveals that the opiate reduces EPSP quantal content at this synapse without altering quantal size. Therefore, the opiate action is presynaptic and affects transmitter release rather than postsynaptic responsiveness.

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ISSN
0036-8075
DOI
10.1126/science.204015
pmid
204015

Abstract

The opiate etorphine depresses monosynaptic excitatory postsynaptic potentials (EPSP's) elicited in spinal cord cells by activation of dorsal root ganglion cells in murine neuronal cell culture. The depression is reversed by naloxone. Statistical analysis of the synaptic responses reveals that the opiate reduces EPSP quantal content at this synapse without altering quantal size. Therefore, the opiate action is presynaptic and affects transmitter release rather than postsynaptic responsiveness.

Journal

Science (New York, N.Y.)Pubmed

Published: Apr 26, 1978

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