Different forms of homeostatic plasticity are engaged with distinct temporal profiles
Global changes in network activity have been reported to induce homeostatic plasticity at multiple synaptic and cellular loci. Though individual types of plasticity are normally examined in isolation, it is their interactions and net effect that will ultimately determine their functional consequence...
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Veröffentlicht in: | The European journal of neuroscience 2006-03, Vol.23 (6), p.1575-1584 |
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description | Global changes in network activity have been reported to induce homeostatic plasticity at multiple synaptic and cellular loci. Though individual types of plasticity are normally examined in isolation, it is their interactions and net effect that will ultimately determine their functional consequences. Here we examine homeostatic plasticity of both inhibition and intrinsic excitability in parallel in rat organotypic hippocampal slices. As previous studies have not examined inhibitory plasticity using a functional measure, inhibition was measured by the ability of evoked inhibitory postsynaptic potentials (IPSPs) to suppress action potentials, as well as IPSP amplitude. We show that manipulations of network activity can both up‐ and downregulate functional inhibition, as well as intrinsic excitability. However, these forms of plasticity are dissociable. Specifically, robust changes in intrinsic excitability were observed in the absence of inhibitory plasticity, and shifts in inhibition, but not excitability, appear to be sensitive to developmental stage. Our data establish that while the two forms of homeostatic plasticity can be engaged in parallel, there is a specific order in which they are expressed, with changes in excitability preceding those in inhibition. We propose that changes in intrinsic excitability occur first in order to stabilize network activity while optimizing the preservation of information stored in synaptic strengths by restricting changes that will disrupt the balance of synaptic excitation and inhibition. |
doi_str_mv | 10.1111/j.1460-9568.2006.04692.x |
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Though individual types of plasticity are normally examined in isolation, it is their interactions and net effect that will ultimately determine their functional consequences. Here we examine homeostatic plasticity of both inhibition and intrinsic excitability in parallel in rat organotypic hippocampal slices. As previous studies have not examined inhibitory plasticity using a functional measure, inhibition was measured by the ability of evoked inhibitory postsynaptic potentials (IPSPs) to suppress action potentials, as well as IPSP amplitude. We show that manipulations of network activity can both up‐ and downregulate functional inhibition, as well as intrinsic excitability. However, these forms of plasticity are dissociable. Specifically, robust changes in intrinsic excitability were observed in the absence of inhibitory plasticity, and shifts in inhibition, but not excitability, appear to be sensitive to developmental stage. Our data establish that while the two forms of homeostatic plasticity can be engaged in parallel, there is a specific order in which they are expressed, with changes in excitability preceding those in inhibition. 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Though individual types of plasticity are normally examined in isolation, it is their interactions and net effect that will ultimately determine their functional consequences. Here we examine homeostatic plasticity of both inhibition and intrinsic excitability in parallel in rat organotypic hippocampal slices. As previous studies have not examined inhibitory plasticity using a functional measure, inhibition was measured by the ability of evoked inhibitory postsynaptic potentials (IPSPs) to suppress action potentials, as well as IPSP amplitude. We show that manipulations of network activity can both up‐ and downregulate functional inhibition, as well as intrinsic excitability. However, these forms of plasticity are dissociable. Specifically, robust changes in intrinsic excitability were observed in the absence of inhibitory plasticity, and shifts in inhibition, but not excitability, appear to be sensitive to developmental stage. Our data establish that while the two forms of homeostatic plasticity can be engaged in parallel, there is a specific order in which they are expressed, with changes in excitability preceding those in inhibition. We propose that changes in intrinsic excitability occur first in order to stabilize network activity while optimizing the preservation of information stored in synaptic strengths by restricting changes that will disrupt the balance of synaptic excitation and inhibition.</description><subject>2-Amino-5-phosphonovalerate - pharmacology</subject><subject>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology</subject><subject>Animals</subject><subject>development</subject><subject>Electrophysiology</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - physiology</subject><subject>Homeostasis - drug effects</subject><subject>Homeostasis - physiology</subject><subject>inhibition</subject><subject>intrinsic excitability</subject><subject>Motor Activity - physiology</subject><subject>Nerve Net - drug effects</subject><subject>Nerve Net - physiology</subject><subject>Neuronal Plasticity - drug effects</subject><subject>Neuronal Plasticity - physiology</subject><subject>Organ Culture Techniques</subject><subject>Patch-Clamp Techniques</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Tetrodotoxin - pharmacology</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1P3DAQhq2qqCzQv1D5hHpJsOPvQw-Ij-VjoYCK2ptlkjFkm2wWOyt2_z0Ou4JbVV_G0jzvzOhBCFOS0_QOpjnlkmRGSJ0XhMiccGmKfPkJjd4bn9GIGMEyTeWfbbQT45QQoiUXX9A2lUIwWdARuj-uvYcAsx77LrQRdx4_dS10sXd9XeJ542Kqdb_CLgCG2aN7hAq_1P0TrurUmpU97qGdd8E1eB46XzcQ99CWd02Er5u6i-5PT34dnWWTn-Pzo8NJVg73ZtSXD1UliXPaV5ozRbnxzAtFKqNJVVBgpeOqNN4bRcAYrZUqQJsCBCeMsF20v56bFj8vIPa2rWMJTeNm0C2ipYoqLoRO4Pd_g5zrghqpZEL1Gi1DF2MAb-ehbl1YWUrsYN9O7SDZDpLtYN--2bfLFP222bJ4aKH6CG50J-DHGnhJllb_PdieXFwPv5TP1vlkHpbveRf-WqmYEvb39dheXdzSy5vJnR2zV4Wxovw</recordid><startdate>200603</startdate><enddate>200603</enddate><creator>Karmarkar, Uma R.</creator><creator>Buonomano, Dean V.</creator><general>Blackwell Publishing Ltd</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>7TK</scope></search><sort><creationdate>200603</creationdate><title>Different forms of homeostatic plasticity are engaged with distinct temporal profiles</title><author>Karmarkar, Uma R. ; Buonomano, Dean V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4692-1fcbdd60aa8fd8437149f3f570d980d21e3ca47c9ff970e9988772e892e540303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>2-Amino-5-phosphonovalerate - pharmacology</topic><topic>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology</topic><topic>Animals</topic><topic>development</topic><topic>Electrophysiology</topic><topic>Excitatory Amino Acid Antagonists - pharmacology</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - physiology</topic><topic>Homeostasis - drug effects</topic><topic>Homeostasis - physiology</topic><topic>inhibition</topic><topic>intrinsic excitability</topic><topic>Motor Activity - physiology</topic><topic>Nerve Net - drug effects</topic><topic>Nerve Net - physiology</topic><topic>Neuronal Plasticity - drug effects</topic><topic>Neuronal Plasticity - physiology</topic><topic>Organ Culture Techniques</topic><topic>Patch-Clamp Techniques</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Tetrodotoxin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karmarkar, Uma R.</creatorcontrib><creatorcontrib>Buonomano, Dean V.</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>Neurosciences Abstracts</collection><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karmarkar, Uma R.</au><au>Buonomano, Dean V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different forms of homeostatic plasticity are engaged with distinct temporal profiles</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2006-03</date><risdate>2006</risdate><volume>23</volume><issue>6</issue><spage>1575</spage><epage>1584</epage><pages>1575-1584</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Global changes in network activity have been reported to induce homeostatic plasticity at multiple synaptic and cellular loci. Though individual types of plasticity are normally examined in isolation, it is their interactions and net effect that will ultimately determine their functional consequences. Here we examine homeostatic plasticity of both inhibition and intrinsic excitability in parallel in rat organotypic hippocampal slices. As previous studies have not examined inhibitory plasticity using a functional measure, inhibition was measured by the ability of evoked inhibitory postsynaptic potentials (IPSPs) to suppress action potentials, as well as IPSP amplitude. We show that manipulations of network activity can both up‐ and downregulate functional inhibition, as well as intrinsic excitability. However, these forms of plasticity are dissociable. Specifically, robust changes in intrinsic excitability were observed in the absence of inhibitory plasticity, and shifts in inhibition, but not excitability, appear to be sensitive to developmental stage. Our data establish that while the two forms of homeostatic plasticity can be engaged in parallel, there is a specific order in which they are expressed, with changes in excitability preceding those in inhibition. We propose that changes in intrinsic excitability occur first in order to stabilize network activity while optimizing the preservation of information stored in synaptic strengths by restricting changes that will disrupt the balance of synaptic excitation and inhibition.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16553621</pmid><doi>10.1111/j.1460-9568.2006.04692.x</doi><tpages>10</tpages></addata></record> |
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subjects | 2-Amino-5-phosphonovalerate - pharmacology 6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology Animals development Electrophysiology Excitatory Amino Acid Antagonists - pharmacology Excitatory Postsynaptic Potentials - physiology hippocampus Hippocampus - drug effects Hippocampus - physiology Homeostasis - drug effects Homeostasis - physiology inhibition intrinsic excitability Motor Activity - physiology Nerve Net - drug effects Nerve Net - physiology Neuronal Plasticity - drug effects Neuronal Plasticity - physiology Organ Culture Techniques Patch-Clamp Techniques rat Rats Rats, Sprague-Dawley Tetrodotoxin - pharmacology |
title | Different forms of homeostatic plasticity are engaged with distinct temporal profiles |
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