High activity K+ channels in rat hippocampal neurones maintained in culture
A channel was identified in cell-attached recordings in rat hippocampal neurones maintained in culture. This channel, which was highly active at the resting membrane potential, was present in most (73 %) patches studied. The channel was characterized by long duration openings and a high open probabi...
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Veröffentlicht in: | Experimental physiology 1999-05, Vol.84 (3), p.501-514, Article S0958067099018242 |
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description | A channel was identified in cell-attached recordings in rat hippocampal neurones maintained in culture. This channel, which was highly active at the resting membrane potential, was present in most (73 %) patches studied. The channel was characterized by long duration openings and a high open probability (Po, mean value 0·73 at -70 mV) at negative patch potentials with mild voltage dependence over the range -40 to -120 mV. It showed inward rectification. There were up to five active channels in cell-attached recordings in experiments where the cells were bathed in sodium-containing Locke solution. The single channel conductances in cell-attached recordings with 140 or 40 mM K+ in the patch pipette were 26 and 12 pS, respectively. The channel was therefore selective for K+ over Na+. The channel was not permeable to Rb+ ions. The single channel conductance was 24 pS in excised inside-out patches bathed in symmetrical K+ (140 mM) solutions. Examination of the channel kinetics revealed that both the open and closed time distributions could be fitted by the sum of three exponentials, there being no pronounced voltage sensitivity between -60 and -120 mV. The 26 pS K+ channel was insensitive to extracellular TEA, apamin, 4-AP and dequalinium. Neither was it sensitive to intracellular Ca2+. Extracellular Ba2+ was effective in reversibly blocking the channel, the IC50 being 2.0 mM. There was no obvious effect of bath application of the K+ channel opener, lemakalim, or a cAMP analogue. This channel appears to contribute a significant proportion (at least 30 %) of the resting conductance in these neurones. |
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T. ; GOODWIN, P. A. ; RICHARDS, C. D.</creator><creatorcontrib>WANN, K. T. ; GOODWIN, P. A. ; RICHARDS, C. D.</creatorcontrib><description>A channel was identified in cell-attached recordings in rat hippocampal neurones maintained in culture. This channel, which was highly active at the resting membrane potential, was present in most (73 %) patches studied. The channel was characterized by long duration openings and a high open probability (Po, mean value 0·73 at -70 mV) at negative patch potentials with mild voltage dependence over the range -40 to -120 mV. It showed inward rectification. There were up to five active channels in cell-attached recordings in experiments where the cells were bathed in sodium-containing Locke solution. The single channel conductances in cell-attached recordings with 140 or 40 mM K+ in the patch pipette were 26 and 12 pS, respectively. The channel was therefore selective for K+ over Na+. The channel was not permeable to Rb+ ions. The single channel conductance was 24 pS in excised inside-out patches bathed in symmetrical K+ (140 mM) solutions. Examination of the channel kinetics revealed that both the open and closed time distributions could be fitted by the sum of three exponentials, there being no pronounced voltage sensitivity between -60 and -120 mV. The 26 pS K+ channel was insensitive to extracellular TEA, apamin, 4-AP and dequalinium. Neither was it sensitive to intracellular Ca2+. Extracellular Ba2+ was effective in reversibly blocking the channel, the IC50 being 2.0 mM. There was no obvious effect of bath application of the K+ channel opener, lemakalim, or a cAMP analogue. This channel appears to contribute a significant proportion (at least 30 %) of the resting conductance in these neurones.</description><identifier>ISSN: 0958-0670</identifier><identifier>EISSN: 1469-445X</identifier><identifier>DOI: 10.1017/S0958067099018242</identifier><identifier>PMID: 10362848</identifier><language>eng</language><publisher>England: Cambridge University Press</publisher><subject>Animals ; Cells, Cultured ; Cromakalim - pharmacology ; Cyclic AMP - analogs & derivatives ; Cyclic AMP - pharmacology ; Hippocampus - cytology ; Hippocampus - metabolism ; Kinetics ; Membrane Potentials ; Neurons - drug effects ; Neurons - metabolism ; Patch-Clamp Techniques ; Potassium Channel Blockers ; Potassium Channels - metabolism ; Rats ; Thionucleotides - pharmacology</subject><ispartof>Experimental physiology, 1999-05, Vol.84 (3), p.501-514, Article S0958067099018242</ispartof><rights>The Physiological Society 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10362848$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WANN, K. T.</creatorcontrib><creatorcontrib>GOODWIN, P. A.</creatorcontrib><creatorcontrib>RICHARDS, C. D.</creatorcontrib><title>High activity K+ channels in rat hippocampal neurones maintained in culture</title><title>Experimental physiology</title><addtitle>Exp. physiol</addtitle><description>A channel was identified in cell-attached recordings in rat hippocampal neurones maintained in culture. This channel, which was highly active at the resting membrane potential, was present in most (73 %) patches studied. The channel was characterized by long duration openings and a high open probability (Po, mean value 0·73 at -70 mV) at negative patch potentials with mild voltage dependence over the range -40 to -120 mV. It showed inward rectification. There were up to five active channels in cell-attached recordings in experiments where the cells were bathed in sodium-containing Locke solution. The single channel conductances in cell-attached recordings with 140 or 40 mM K+ in the patch pipette were 26 and 12 pS, respectively. The channel was therefore selective for K+ over Na+. The channel was not permeable to Rb+ ions. The single channel conductance was 24 pS in excised inside-out patches bathed in symmetrical K+ (140 mM) solutions. Examination of the channel kinetics revealed that both the open and closed time distributions could be fitted by the sum of three exponentials, there being no pronounced voltage sensitivity between -60 and -120 mV. The 26 pS K+ channel was insensitive to extracellular TEA, apamin, 4-AP and dequalinium. Neither was it sensitive to intracellular Ca2+. Extracellular Ba2+ was effective in reversibly blocking the channel, the IC50 being 2.0 mM. There was no obvious effect of bath application of the K+ channel opener, lemakalim, or a cAMP analogue. This channel appears to contribute a significant proportion (at least 30 %) of the resting conductance in these neurones.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Cromakalim - pharmacology</subject><subject>Cyclic AMP - analogs & derivatives</subject><subject>Cyclic AMP - pharmacology</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - metabolism</subject><subject>Kinetics</subject><subject>Membrane Potentials</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Patch-Clamp Techniques</subject><subject>Potassium Channel Blockers</subject><subject>Potassium Channels - metabolism</subject><subject>Rats</subject><subject>Thionucleotides - pharmacology</subject><issn>0958-0670</issn><issn>1469-445X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxDAUhYMozjj6A9xIV26kmlfTdimDOjKCCxXchTS9nWboyyRV-u9tmQEFwcXlwj3n3AMfQucEXxNM4psXnEYJFjFOU0wSyukBmhMu0pDz6P0QzSc5nPQZOnFuizFhOOHHaEYwEzThyRytV2ZTBkp782n8EKyvAl2qpoHKBaYJrPJBabqu1aruVBU00Nu2ARfUyjR-HMgnm-4r31s4RUeFqhyc7fcCvd3fvS5X4dPzw-Py9inUjHIf5iJVuWBxITImeE4xxDrjERWkSDSlivCUcRYziKniirCYM2A4Y-MpwlwDW6DL3d_Oth89OC9r4zRUlWqg7Z0UaTKmSDwayc6obeuchUJ21tTKDpJgORGUfwiOmYv98z6rIf-V2CH7aS9Hcl_GguzKwZnWtdqAH2TCJZPRiHqB2L5d1Zk1-Qbktu1tM6L5p_8bbhaHVw</recordid><startdate>19990501</startdate><enddate>19990501</enddate><creator>WANN, K. T.</creator><creator>GOODWIN, P. A.</creator><creator>RICHARDS, C. D.</creator><general>Cambridge University Press</general><general>The Physiological Society</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>7X8</scope></search><sort><creationdate>19990501</creationdate><title>High activity K+ channels in rat hippocampal neurones maintained in culture</title><author>WANN, K. T. ; GOODWIN, P. A. ; RICHARDS, C. D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c324t-d69ad637f6b364d20e7cb45261f8c22a14934373e72a4a13743e30b3373504ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Cromakalim - pharmacology</topic><topic>Cyclic AMP - analogs & derivatives</topic><topic>Cyclic AMP - pharmacology</topic><topic>Hippocampus - cytology</topic><topic>Hippocampus - metabolism</topic><topic>Kinetics</topic><topic>Membrane Potentials</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Patch-Clamp Techniques</topic><topic>Potassium Channel Blockers</topic><topic>Potassium Channels - metabolism</topic><topic>Rats</topic><topic>Thionucleotides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WANN, K. T.</creatorcontrib><creatorcontrib>GOODWIN, P. A.</creatorcontrib><creatorcontrib>RICHARDS, C. D.</creatorcontrib><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>Experimental physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WANN, K. T.</au><au>GOODWIN, P. A.</au><au>RICHARDS, C. D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High activity K+ channels in rat hippocampal neurones maintained in culture</atitle><jtitle>Experimental physiology</jtitle><addtitle>Exp. physiol</addtitle><date>1999-05-01</date><risdate>1999</risdate><volume>84</volume><issue>3</issue><spage>501</spage><epage>514</epage><pages>501-514</pages><artnum>S0958067099018242</artnum><issn>0958-0670</issn><eissn>1469-445X</eissn><abstract>A channel was identified in cell-attached recordings in rat hippocampal neurones maintained in culture. This channel, which was highly active at the resting membrane potential, was present in most (73 %) patches studied. The channel was characterized by long duration openings and a high open probability (Po, mean value 0·73 at -70 mV) at negative patch potentials with mild voltage dependence over the range -40 to -120 mV. It showed inward rectification. There were up to five active channels in cell-attached recordings in experiments where the cells were bathed in sodium-containing Locke solution. The single channel conductances in cell-attached recordings with 140 or 40 mM K+ in the patch pipette were 26 and 12 pS, respectively. The channel was therefore selective for K+ over Na+. The channel was not permeable to Rb+ ions. The single channel conductance was 24 pS in excised inside-out patches bathed in symmetrical K+ (140 mM) solutions. Examination of the channel kinetics revealed that both the open and closed time distributions could be fitted by the sum of three exponentials, there being no pronounced voltage sensitivity between -60 and -120 mV. The 26 pS K+ channel was insensitive to extracellular TEA, apamin, 4-AP and dequalinium. Neither was it sensitive to intracellular Ca2+. Extracellular Ba2+ was effective in reversibly blocking the channel, the IC50 being 2.0 mM. There was no obvious effect of bath application of the K+ channel opener, lemakalim, or a cAMP analogue. This channel appears to contribute a significant proportion (at least 30 %) of the resting conductance in these neurones.</abstract><cop>England</cop><pub>Cambridge University Press</pub><pmid>10362848</pmid><doi>10.1017/S0958067099018242</doi><tpages>14</tpages></addata></record> |
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subjects | Animals Cells, Cultured Cromakalim - pharmacology Cyclic AMP - analogs & derivatives Cyclic AMP - pharmacology Hippocampus - cytology Hippocampus - metabolism Kinetics Membrane Potentials Neurons - drug effects Neurons - metabolism Patch-Clamp Techniques Potassium Channel Blockers Potassium Channels - metabolism Rats Thionucleotides - pharmacology |
title | High activity K+ channels in rat hippocampal neurones maintained in culture |
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