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Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences

A computationally rich algorithm of synaptic plasticity has been proposed based on the experimental observation that the sign and amplitude of the change in synaptic weight is dictated by the temporal order and temporal contiguity between pre- and postsynaptic activities. For more than a decade, thi...

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Detalles Bibliográficos
Autores principales: Shulz, Daniel E., Jacob, Vincent
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3059664/
https://www.ncbi.nlm.nih.gov/pubmed/21423523
http://dx.doi.org/10.3389/fnsyn.2010.00137
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author Shulz, Daniel E.
Jacob, Vincent
author_facet Shulz, Daniel E.
Jacob, Vincent
author_sort Shulz, Daniel E.
collection PubMed
description A computationally rich algorithm of synaptic plasticity has been proposed based on the experimental observation that the sign and amplitude of the change in synaptic weight is dictated by the temporal order and temporal contiguity between pre- and postsynaptic activities. For more than a decade, this spike-timing-dependent plasticity (STDP) has been studied mainly in brain slices of different brain structures and cultured neurons. Although not yet compelling, evidences for the STDP rule in the intact brain, including primary sensory cortices, have been provided lastly. From insects to mammals, the presentation of precisely timed sensory inputs drives synaptic and functional plasticity in the intact central nervous system, with similar timing requirements than the in vitro defined STDP rule. The convergent evolution of this plasticity rule in species belonging to so distant phylogenic groups points to the efficiency of STDP, as a mechanism for modifying synaptic weights, as the basis of activity-dependent development, learning and memory. In spite of the ubiquity of STDP phenomena, a number of significant variations of the rule are observed in different structures, neuronal types and even synapses on the same neuron, as well as between in vitro and in vivo conditions. In addition, the state of the neuronal network, its ongoing activity and the activation of ascending neuromodulatory systems in different behavioral conditions have dramatic consequences on the expression of spike-timing-dependent synaptic plasticity, and should be further explored.
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spelling pubmed-30596642011-03-21 Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences Shulz, Daniel E. Jacob, Vincent Front Synaptic Neurosci Neuroscience A computationally rich algorithm of synaptic plasticity has been proposed based on the experimental observation that the sign and amplitude of the change in synaptic weight is dictated by the temporal order and temporal contiguity between pre- and postsynaptic activities. For more than a decade, this spike-timing-dependent plasticity (STDP) has been studied mainly in brain slices of different brain structures and cultured neurons. Although not yet compelling, evidences for the STDP rule in the intact brain, including primary sensory cortices, have been provided lastly. From insects to mammals, the presentation of precisely timed sensory inputs drives synaptic and functional plasticity in the intact central nervous system, with similar timing requirements than the in vitro defined STDP rule. The convergent evolution of this plasticity rule in species belonging to so distant phylogenic groups points to the efficiency of STDP, as a mechanism for modifying synaptic weights, as the basis of activity-dependent development, learning and memory. In spite of the ubiquity of STDP phenomena, a number of significant variations of the rule are observed in different structures, neuronal types and even synapses on the same neuron, as well as between in vitro and in vivo conditions. In addition, the state of the neuronal network, its ongoing activity and the activation of ascending neuromodulatory systems in different behavioral conditions have dramatic consequences on the expression of spike-timing-dependent synaptic plasticity, and should be further explored. Frontiers Research Foundation 2010-08-24 /pmc/articles/PMC3059664/ /pubmed/21423523 http://dx.doi.org/10.3389/fnsyn.2010.00137 Text en Copyright © 2010 Shulz and Jacob. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Shulz, Daniel E.
Jacob, Vincent
Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences
title Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences
title_full Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences
title_fullStr Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences
title_full_unstemmed Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences
title_short Spike-Timing-Dependent Plasticity in the Intact Brain: Counteracting Spurious Spike Coincidences
title_sort spike-timing-dependent plasticity in the intact brain: counteracting spurious spike coincidences
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3059664/
https://www.ncbi.nlm.nih.gov/pubmed/21423523
http://dx.doi.org/10.3389/fnsyn.2010.00137
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