Modulation of Ether-à-Go-Go Related Gene (ERG) Current Governs Intrinsic Persistent Activity in Rodent Neocortical Pyramidal Cells
While cholinergic receptor activation has long been known to dramatically enhance the excitability of cortical neurons, the cellular mechanisms responsible for this effect are not well understood. We used intracellular recordings in rat (both sexes) neocortical brain slices to assess the ionic mecha...
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description | While cholinergic receptor activation has long been known to dramatically enhance the excitability of cortical neurons, the cellular mechanisms responsible for this effect are not well understood. We used intracellular recordings in rat (both sexes) neocortical brain slices to assess the ionic mechanisms supporting persistent firing modes triggered by depolarizing stimuli following cholinergic receptor activation. We found multiple lines of evidence suggesting that a component of the underlying hyperexcitability associated with persistent firing reflects a reduction in the standing (leak) K
current mediated by Ether-a-go-go-Related Gene (ERG) channels. Three chemically diverse ERG channel blockers (terfenadine, ErgToxin-1, and E-4031) abolished persistent firing and the underlying increase in input resistance in deep pyramidal cells in temporal and prefrontal association neocortex. Calcium accumulation during triggering stimuli appears to attenuate ERG currents, leading to membrane potential depolarization and increased input resistance, two critical elements generating persistent firing. Our results also suggest that ERG current normally governs cortical neuron responses to depolarizing stimuli by opposing prolonged discharges and by enhancing the poststimulus repolarization. The broad expression of ERG channels and the ability of ERG blocks to abolish persistent firing evoked by both synaptic and intracellular step stimuli suggest that modulation of ERG channels may underlie many forms of persistent activity observed
Persistent activity, where spiking continues beyond the triggering stimulus, is a common phenomenon observed in many types of neurons. Identifying the mechanism underlying this elementary process of memory is a step forward in understanding higher cognitive function including short-term memory. Our results suggest that a reduction in the currents normally mediated by Ether-a-go-go-Related Gene (ERG) K
channels contributes to persistent firing in neocortical pyramidal cells. ERG currents have been previously studied primarily in the heart; relatively little is known about ERG function in the brain, although mutations in ERG channels have recently been linked to schizophrenia. The present study is among the first to describe its role in neocortex in relation to biophysical correlates of memory function. |
doi_str_mv | 10.1523/JNEUROSCI.1774-17.2017 |
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current mediated by Ether-a-go-go-Related Gene (ERG) channels. Three chemically diverse ERG channel blockers (terfenadine, ErgToxin-1, and E-4031) abolished persistent firing and the underlying increase in input resistance in deep pyramidal cells in temporal and prefrontal association neocortex. Calcium accumulation during triggering stimuli appears to attenuate ERG currents, leading to membrane potential depolarization and increased input resistance, two critical elements generating persistent firing. Our results also suggest that ERG current normally governs cortical neuron responses to depolarizing stimuli by opposing prolonged discharges and by enhancing the poststimulus repolarization. The broad expression of ERG channels and the ability of ERG blocks to abolish persistent firing evoked by both synaptic and intracellular step stimuli suggest that modulation of ERG channels may underlie many forms of persistent activity observed
Persistent activity, where spiking continues beyond the triggering stimulus, is a common phenomenon observed in many types of neurons. Identifying the mechanism underlying this elementary process of memory is a step forward in understanding higher cognitive function including short-term memory. Our results suggest that a reduction in the currents normally mediated by Ether-a-go-go-Related Gene (ERG) K
channels contributes to persistent firing in neocortical pyramidal cells. ERG currents have been previously studied primarily in the heart; relatively little is known about ERG function in the brain, although mutations in ERG channels have recently been linked to schizophrenia. The present study is among the first to describe its role in neocortex in relation to biophysical correlates of memory function.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.1774-17.2017</identifier><identifier>PMID: 29175952</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Acetylcholine receptors ; Action Potentials - physiology ; Activation ; Animals ; Brain ; Brain slice preparation ; Calcium ; Channels ; Cognitive ability ; Depolarization ; Electroretinograms ; Ether-A-Go-Go Potassium Channels - metabolism ; Excitability ; Female ; Firing pattern ; Intracellular ; Male ; Membrane potential ; Memory ; Mental disorders ; Modulation ; Mutation ; Neocortex - physiology ; Neurons ; Organic chemistry ; Potassium ; Pyramidal cells ; Pyramidal Cells - metabolism ; Rats ; Rats, Sprague-Dawley ; Receptor mechanisms ; Reduction ; Schizophrenia ; Short term memory ; Stimuli ; Terfenadine</subject><ispartof>The Journal of neuroscience, 2018-01, Vol.38 (2), p.423-440</ispartof><rights>Copyright © 2018 the authors 0270-6474/18/380423-18$15.00/0.</rights><rights>Copyright Society for Neuroscience Jan 10, 2018</rights><rights>Copyright © 2018 the authors 0270-6474/18/380423-18$15.00/0 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-5aca8407b218941ee8cf00b4a6aa33fac897735953f708b5d7df6e6687acee983</citedby><cites>FETCH-LOGICAL-c442t-5aca8407b218941ee8cf00b4a6aa33fac897735953f708b5d7df6e6687acee983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5761618/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5761618/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29175952$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cui, Edward D</creatorcontrib><creatorcontrib>Strowbridge, Ben W</creatorcontrib><title>Modulation of Ether-à-Go-Go Related Gene (ERG) Current Governs Intrinsic Persistent Activity in Rodent Neocortical Pyramidal Cells</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>While cholinergic receptor activation has long been known to dramatically enhance the excitability of cortical neurons, the cellular mechanisms responsible for this effect are not well understood. We used intracellular recordings in rat (both sexes) neocortical brain slices to assess the ionic mechanisms supporting persistent firing modes triggered by depolarizing stimuli following cholinergic receptor activation. We found multiple lines of evidence suggesting that a component of the underlying hyperexcitability associated with persistent firing reflects a reduction in the standing (leak) K
current mediated by Ether-a-go-go-Related Gene (ERG) channels. Three chemically diverse ERG channel blockers (terfenadine, ErgToxin-1, and E-4031) abolished persistent firing and the underlying increase in input resistance in deep pyramidal cells in temporal and prefrontal association neocortex. Calcium accumulation during triggering stimuli appears to attenuate ERG currents, leading to membrane potential depolarization and increased input resistance, two critical elements generating persistent firing. Our results also suggest that ERG current normally governs cortical neuron responses to depolarizing stimuli by opposing prolonged discharges and by enhancing the poststimulus repolarization. The broad expression of ERG channels and the ability of ERG blocks to abolish persistent firing evoked by both synaptic and intracellular step stimuli suggest that modulation of ERG channels may underlie many forms of persistent activity observed
Persistent activity, where spiking continues beyond the triggering stimulus, is a common phenomenon observed in many types of neurons. Identifying the mechanism underlying this elementary process of memory is a step forward in understanding higher cognitive function including short-term memory. Our results suggest that a reduction in the currents normally mediated by Ether-a-go-go-Related Gene (ERG) K
channels contributes to persistent firing in neocortical pyramidal cells. ERG currents have been previously studied primarily in the heart; relatively little is known about ERG function in the brain, although mutations in ERG channels have recently been linked to schizophrenia. The present study is among the first to describe its role in neocortex in relation to biophysical correlates of memory function.</description><subject>Acetylcholine receptors</subject><subject>Action Potentials - physiology</subject><subject>Activation</subject><subject>Animals</subject><subject>Brain</subject><subject>Brain slice preparation</subject><subject>Calcium</subject><subject>Channels</subject><subject>Cognitive ability</subject><subject>Depolarization</subject><subject>Electroretinograms</subject><subject>Ether-A-Go-Go Potassium Channels - metabolism</subject><subject>Excitability</subject><subject>Female</subject><subject>Firing pattern</subject><subject>Intracellular</subject><subject>Male</subject><subject>Membrane potential</subject><subject>Memory</subject><subject>Mental disorders</subject><subject>Modulation</subject><subject>Mutation</subject><subject>Neocortex - physiology</subject><subject>Neurons</subject><subject>Organic chemistry</subject><subject>Potassium</subject><subject>Pyramidal cells</subject><subject>Pyramidal Cells - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor mechanisms</subject><subject>Reduction</subject><subject>Schizophrenia</subject><subject>Short term memory</subject><subject>Stimuli</subject><subject>Terfenadine</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkcFq3DAQhkVpaLZpXyEIekkP3ki2bFmXQjBbd0OahG1zFlp53Ch4pUSSF_bcF8m75MUqk2RpC0Ia9P8zzM-H0DElc1rmxen55eJmdfWjWc4p5yyjfJ4Tyt-gWVJFljNC36IZyTnJKsbZIXofwh0hhCfTO3SYC8pLUeYz9Pu768ZBReMsdj1exFvw2dNj1rp08AqSBB1uwQI-Wazaz7gZvQcbceu24G3ASxu9scFofA0-mBAn8UxHszVxh43FK9dNX5fgtPPRaDXg651XG9OlqoFhCB_QQa-GAB9f3iN083Xxs_mWXVy1y-bsItOM5TErlVY1I3yd01owClDrnpA1U5VSRdErXQvOixSr6Dmp12XHu76Cqqq50gCiLo7Ql-e59-N6A51Oa3k1yHtvNsrvpFNG_qtYcyt_ua0seUUrOg04eRng3cMIIcqNCTpFUBbcGCQVlRAF5yVN1k__We_c6G2KJ3MiGKsTxDK5qmeX9i4ED_1-GUrkxFnuOcuJc7rkxDk1Hv8dZd_2Crb4A-lQpvo</recordid><startdate>20180110</startdate><enddate>20180110</enddate><creator>Cui, Edward D</creator><creator>Strowbridge, Ben W</creator><general>Society for Neuroscience</general><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>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180110</creationdate><title>Modulation of Ether-à-Go-Go Related Gene (ERG) Current Governs Intrinsic Persistent Activity in Rodent Neocortical Pyramidal Cells</title><author>Cui, Edward D ; Strowbridge, Ben W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-5aca8407b218941ee8cf00b4a6aa33fac897735953f708b5d7df6e6687acee983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetylcholine receptors</topic><topic>Action Potentials - physiology</topic><topic>Activation</topic><topic>Animals</topic><topic>Brain</topic><topic>Brain slice preparation</topic><topic>Calcium</topic><topic>Channels</topic><topic>Cognitive ability</topic><topic>Depolarization</topic><topic>Electroretinograms</topic><topic>Ether-A-Go-Go Potassium Channels - metabolism</topic><topic>Excitability</topic><topic>Female</topic><topic>Firing pattern</topic><topic>Intracellular</topic><topic>Male</topic><topic>Membrane potential</topic><topic>Memory</topic><topic>Mental disorders</topic><topic>Modulation</topic><topic>Mutation</topic><topic>Neocortex - physiology</topic><topic>Neurons</topic><topic>Organic chemistry</topic><topic>Potassium</topic><topic>Pyramidal cells</topic><topic>Pyramidal Cells - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor mechanisms</topic><topic>Reduction</topic><topic>Schizophrenia</topic><topic>Short term memory</topic><topic>Stimuli</topic><topic>Terfenadine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cui, Edward D</creatorcontrib><creatorcontrib>Strowbridge, Ben W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cui, Edward D</au><au>Strowbridge, Ben W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of Ether-à-Go-Go Related Gene (ERG) Current Governs Intrinsic Persistent Activity in Rodent Neocortical Pyramidal Cells</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2018-01-10</date><risdate>2018</risdate><volume>38</volume><issue>2</issue><spage>423</spage><epage>440</epage><pages>423-440</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>While cholinergic receptor activation has long been known to dramatically enhance the excitability of cortical neurons, the cellular mechanisms responsible for this effect are not well understood. We used intracellular recordings in rat (both sexes) neocortical brain slices to assess the ionic mechanisms supporting persistent firing modes triggered by depolarizing stimuli following cholinergic receptor activation. We found multiple lines of evidence suggesting that a component of the underlying hyperexcitability associated with persistent firing reflects a reduction in the standing (leak) K
current mediated by Ether-a-go-go-Related Gene (ERG) channels. Three chemically diverse ERG channel blockers (terfenadine, ErgToxin-1, and E-4031) abolished persistent firing and the underlying increase in input resistance in deep pyramidal cells in temporal and prefrontal association neocortex. Calcium accumulation during triggering stimuli appears to attenuate ERG currents, leading to membrane potential depolarization and increased input resistance, two critical elements generating persistent firing. Our results also suggest that ERG current normally governs cortical neuron responses to depolarizing stimuli by opposing prolonged discharges and by enhancing the poststimulus repolarization. The broad expression of ERG channels and the ability of ERG blocks to abolish persistent firing evoked by both synaptic and intracellular step stimuli suggest that modulation of ERG channels may underlie many forms of persistent activity observed
Persistent activity, where spiking continues beyond the triggering stimulus, is a common phenomenon observed in many types of neurons. Identifying the mechanism underlying this elementary process of memory is a step forward in understanding higher cognitive function including short-term memory. Our results suggest that a reduction in the currents normally mediated by Ether-a-go-go-Related Gene (ERG) K
channels contributes to persistent firing in neocortical pyramidal cells. ERG currents have been previously studied primarily in the heart; relatively little is known about ERG function in the brain, although mutations in ERG channels have recently been linked to schizophrenia. The present study is among the first to describe its role in neocortex in relation to biophysical correlates of memory function.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>29175952</pmid><doi>10.1523/JNEUROSCI.1774-17.2017</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine receptors Action Potentials - physiology Activation Animals Brain Brain slice preparation Calcium Channels Cognitive ability Depolarization Electroretinograms Ether-A-Go-Go Potassium Channels - metabolism Excitability Female Firing pattern Intracellular Male Membrane potential Memory Mental disorders Modulation Mutation Neocortex - physiology Neurons Organic chemistry Potassium Pyramidal cells Pyramidal Cells - metabolism Rats Rats, Sprague-Dawley Receptor mechanisms Reduction Schizophrenia Short term memory Stimuli Terfenadine |
title | Modulation of Ether-à-Go-Go Related Gene (ERG) Current Governs Intrinsic Persistent Activity in Rodent Neocortical Pyramidal Cells |
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