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Encoding and retrieval in a model of the hippocampal CA1 microcircuit
It has been proposed that the hippocampal theta rhythm (4–7 Hz) can contribute to memory formation by separating encoding (storage) and retrieval of memories into different functional half‐cycles (Hasselmo et al. (2002) Neural Comput 14:793–817). We investigate, via computer simulations, the biophys...
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Published in: | Hippocampus 2010-03, Vol.20 (3), p.423-446 |
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description | It has been proposed that the hippocampal theta rhythm (4–7 Hz) can contribute to memory formation by separating encoding (storage) and retrieval of memories into different functional half‐cycles (Hasselmo et al. (2002) Neural Comput 14:793–817). We investigate, via computer simulations, the biophysical mechanisms by which storage and recall of spatio‐temporal input patterns are achieved by the CA1 microcircuitry. A model of the CA1 microcircuit is presented that uses biophysical representations of the major cell types, including pyramidal (P) cells and four types of inhibitory interneurons: basket (B) cells, axo‐axonic (AA) cells, bistratified (BS) cells and oriens lacunosum‐moleculare (OLM) cells. Inputs to the network come from the entorhinal cortex (EC), the CA3 Schaffer collaterals and medial septum. The EC input provides the sensory information, whereas all other inputs provide context and timing information. Septal input provides timing information for phasing storage and recall. Storage is accomplished via a local STDP mediated hetero‐association of the EC input pattern and the incoming CA3 input pattern on the CA1 pyramidal cell target synapses. The model simulates the timing of firing of different hippocampal cell types relative to the theta rhythm in anesthetized animals and proposes experimentally confirmed functional roles for the different classes of inhibitory interneurons in the storage and recall cycles (Klausberger et al., (2003, 2004) Nature 421:844–848, Nat Neurosci 7:41–47). Measures of recall performance of new and previously stored input patterns in the presence or absence of various inhibitory interneurons are employed to quantitatively test the performance of our model. Finally, the mean recall quality of the CA1 microcircuit is tested as the number of stored patterns is increased. © 2009 Wiley‐Liss, Inc. |
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(2002) Neural Comput 14:793–817). We investigate, via computer simulations, the biophysical mechanisms by which storage and recall of spatio‐temporal input patterns are achieved by the CA1 microcircuitry. A model of the CA1 microcircuit is presented that uses biophysical representations of the major cell types, including pyramidal (P) cells and four types of inhibitory interneurons: basket (B) cells, axo‐axonic (AA) cells, bistratified (BS) cells and oriens lacunosum‐moleculare (OLM) cells. Inputs to the network come from the entorhinal cortex (EC), the CA3 Schaffer collaterals and medial septum. The EC input provides the sensory information, whereas all other inputs provide context and timing information. Septal input provides timing information for phasing storage and recall. Storage is accomplished via a local STDP mediated hetero‐association of the EC input pattern and the incoming CA3 input pattern on the CA1 pyramidal cell target synapses. The model simulates the timing of firing of different hippocampal cell types relative to the theta rhythm in anesthetized animals and proposes experimentally confirmed functional roles for the different classes of inhibitory interneurons in the storage and recall cycles (Klausberger et al., (2003, 2004) Nature 421:844–848, Nat Neurosci 7:41–47). Measures of recall performance of new and previously stored input patterns in the presence or absence of various inhibitory interneurons are employed to quantitatively test the performance of our model. 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(2002) Neural Comput 14:793–817). We investigate, via computer simulations, the biophysical mechanisms by which storage and recall of spatio‐temporal input patterns are achieved by the CA1 microcircuitry. A model of the CA1 microcircuit is presented that uses biophysical representations of the major cell types, including pyramidal (P) cells and four types of inhibitory interneurons: basket (B) cells, axo‐axonic (AA) cells, bistratified (BS) cells and oriens lacunosum‐moleculare (OLM) cells. Inputs to the network come from the entorhinal cortex (EC), the CA3 Schaffer collaterals and medial septum. The EC input provides the sensory information, whereas all other inputs provide context and timing information. Septal input provides timing information for phasing storage and recall. Storage is accomplished via a local STDP mediated hetero‐association of the EC input pattern and the incoming CA3 input pattern on the CA1 pyramidal cell target synapses. The model simulates the timing of firing of different hippocampal cell types relative to the theta rhythm in anesthetized animals and proposes experimentally confirmed functional roles for the different classes of inhibitory interneurons in the storage and recall cycles (Klausberger et al., (2003, 2004) Nature 421:844–848, Nat Neurosci 7:41–47). Measures of recall performance of new and previously stored input patterns in the presence or absence of various inhibitory interneurons are employed to quantitatively test the performance of our model. Finally, the mean recall quality of the CA1 microcircuit is tested as the number of stored patterns is increased. © 2009 Wiley‐Liss, Inc.</description><subject>Action Potentials - physiology</subject><subject>Afferent Pathways - cytology</subject><subject>Afferent Pathways - physiology</subject><subject>Animals</subject><subject>axo-axonic cell</subject><subject>Axons - physiology</subject><subject>Axons - ultrastructure</subject><subject>basket cell</subject><subject>Biological Clocks - physiology</subject><subject>bistratified cell</subject><subject>CA1 microcircuit model</subject><subject>CA1 Region, Hippocampal - cytology</subject><subject>CA1 Region, Hippocampal - physiology</subject><subject>Computer Simulation</subject><subject>Dendrites - physiology</subject><subject>Dendrites - ultrastructure</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>gamma-Aminobutyric Acid - physiology</subject><subject>Humans</subject><subject>Inhibitory Postsynaptic Potentials - physiology</subject><subject>Interneurons - cytology</subject><subject>Interneurons - physiology</subject><subject>Learning - physiology</subject><subject>Memory - physiology</subject><subject>Neural Inhibition - physiology</subject><subject>Neural Pathways - cytology</subject><subject>Neural Pathways - physiology</subject><subject>Neurons - cytology</subject><subject>Neurons - physiology</subject><subject>OLM cell</subject><subject>pyramidal cell</subject><subject>Pyramidal Cells - cytology</subject><subject>Pyramidal Cells - physiology</subject><subject>STDP</subject><subject>storage and recall</subject><subject>Synaptic Transmission - physiology</subject><subject>Theta Rhythm</subject><issn>1050-9631</issn><issn>1098-1063</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EoqWw4QOQd0hIKXacuPGyqvqiqEUCxNJynQk15IWdAP17UlJgx8oj-dwzo4vQOSV9Soh_vTFl0fcJ5_QAdSkRkUcJZ4e7OSSe4Ix20IlzL4RQGhJyjDpUBJFool00Hue6iE3-jFUeYwuVNfCuUmxyrHBWxJDiIsHVBnCzpSy0ysrmdzSkODPaFtpYXZvqFB0lKnVwtn976HEyfhjNvNvVdD4a3no6YD71QMRxonkQQxABTyJN1hSAR4oIwSEMYxABACSR8gWL1kowEFoLzTVXPPEJ66HL1lva4q0GV8nMOA1pqnIoaicHjPmCDnjQkFct2RzpnIVEltZkym4lJXLXmty1Jr9ba-CLvbZeZxD_ofuaGoC2wIdJYfuPSs7md6sfqddmjKvg8zej7KvkAzYI5dNyKvnNPV8uFlM5YV_r0IbS</recordid><startdate>201003</startdate><enddate>201003</enddate><creator>Cutsuridis, Vassilis</creator><creator>Cobb, Stuart</creator><creator>Graham, Bruce P.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201003</creationdate><title>Encoding and retrieval in a model of the hippocampal CA1 microcircuit</title><author>Cutsuridis, Vassilis ; Cobb, Stuart ; Graham, Bruce P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4321-e9ddfc64de48e6f8c0b1ee68a0996e55de94eeef8a2938ba93e9cc9c6c6a6f203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Action Potentials - physiology</topic><topic>Afferent Pathways - cytology</topic><topic>Afferent Pathways - physiology</topic><topic>Animals</topic><topic>axo-axonic cell</topic><topic>Axons - physiology</topic><topic>Axons - ultrastructure</topic><topic>basket cell</topic><topic>Biological Clocks - physiology</topic><topic>bistratified cell</topic><topic>CA1 microcircuit model</topic><topic>CA1 Region, Hippocampal - cytology</topic><topic>CA1 Region, Hippocampal - physiology</topic><topic>Computer Simulation</topic><topic>Dendrites - physiology</topic><topic>Dendrites - ultrastructure</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>gamma-Aminobutyric Acid - physiology</topic><topic>Humans</topic><topic>Inhibitory Postsynaptic Potentials - physiology</topic><topic>Interneurons - cytology</topic><topic>Interneurons - physiology</topic><topic>Learning - physiology</topic><topic>Memory - physiology</topic><topic>Neural Inhibition - physiology</topic><topic>Neural Pathways - cytology</topic><topic>Neural Pathways - physiology</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>OLM cell</topic><topic>pyramidal cell</topic><topic>Pyramidal Cells - cytology</topic><topic>Pyramidal Cells - physiology</topic><topic>STDP</topic><topic>storage and recall</topic><topic>Synaptic Transmission - physiology</topic><topic>Theta Rhythm</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cutsuridis, Vassilis</creatorcontrib><creatorcontrib>Cobb, Stuart</creatorcontrib><creatorcontrib>Graham, Bruce P.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Hippocampus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cutsuridis, Vassilis</au><au>Cobb, Stuart</au><au>Graham, Bruce P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Encoding and retrieval in a model of the hippocampal CA1 microcircuit</atitle><jtitle>Hippocampus</jtitle><addtitle>Hippocampus</addtitle><date>2010-03</date><risdate>2010</risdate><volume>20</volume><issue>3</issue><spage>423</spage><epage>446</epage><pages>423-446</pages><issn>1050-9631</issn><eissn>1098-1063</eissn><abstract>It has been proposed that the hippocampal theta rhythm (4–7 Hz) can contribute to memory formation by separating encoding (storage) and retrieval of memories into different functional half‐cycles (Hasselmo et al. (2002) Neural Comput 14:793–817). We investigate, via computer simulations, the biophysical mechanisms by which storage and recall of spatio‐temporal input patterns are achieved by the CA1 microcircuitry. A model of the CA1 microcircuit is presented that uses biophysical representations of the major cell types, including pyramidal (P) cells and four types of inhibitory interneurons: basket (B) cells, axo‐axonic (AA) cells, bistratified (BS) cells and oriens lacunosum‐moleculare (OLM) cells. Inputs to the network come from the entorhinal cortex (EC), the CA3 Schaffer collaterals and medial septum. The EC input provides the sensory information, whereas all other inputs provide context and timing information. Septal input provides timing information for phasing storage and recall. Storage is accomplished via a local STDP mediated hetero‐association of the EC input pattern and the incoming CA3 input pattern on the CA1 pyramidal cell target synapses. The model simulates the timing of firing of different hippocampal cell types relative to the theta rhythm in anesthetized animals and proposes experimentally confirmed functional roles for the different classes of inhibitory interneurons in the storage and recall cycles (Klausberger et al., (2003, 2004) Nature 421:844–848, Nat Neurosci 7:41–47). Measures of recall performance of new and previously stored input patterns in the presence or absence of various inhibitory interneurons are employed to quantitatively test the performance of our model. Finally, the mean recall quality of the CA1 microcircuit is tested as the number of stored patterns is increased. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19489002</pmid><doi>10.1002/hipo.20661</doi><tpages>24</tpages></addata></record> |
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subjects | Action Potentials - physiology Afferent Pathways - cytology Afferent Pathways - physiology Animals axo-axonic cell Axons - physiology Axons - ultrastructure basket cell Biological Clocks - physiology bistratified cell CA1 microcircuit model CA1 Region, Hippocampal - cytology CA1 Region, Hippocampal - physiology Computer Simulation Dendrites - physiology Dendrites - ultrastructure Excitatory Postsynaptic Potentials - physiology gamma-Aminobutyric Acid - physiology Humans Inhibitory Postsynaptic Potentials - physiology Interneurons - cytology Interneurons - physiology Learning - physiology Memory - physiology Neural Inhibition - physiology Neural Pathways - cytology Neural Pathways - physiology Neurons - cytology Neurons - physiology OLM cell pyramidal cell Pyramidal Cells - cytology Pyramidal Cells - physiology STDP storage and recall Synaptic Transmission - physiology Theta Rhythm |
title | Encoding and retrieval in a model of the hippocampal CA1 microcircuit |
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