Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M sub(1) muscarinic acetylcholine receptors
* KCNQ1-4 potassium channels were expressed in mammalian Chinese hamster ovary (CHO) cells stably transfected with M sub(1) muscarinic acetylcholine receptors and currents were recorded using the whole-cell perforated patch technique and cell-attached patch recording. * Stimulation of M sub(1) recep...
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Veröffentlicht in: | The Journal of physiology 2000-02, Vol.522 (3), p.349-355 |
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creator | Selyanko, A A Hadley, J K Wood, I C Abogadie, F C Jentsch, T J Brown, DA |
description | * KCNQ1-4 potassium channels were expressed in mammalian Chinese hamster ovary (CHO) cells stably transfected with M sub(1) muscarinic acetylcholine receptors and currents were recorded using the whole-cell perforated patch technique and cell-attached patch recording. * Stimulation of M sub(1) receptors by 10 mu m oxotremorine-M (Oxo-M) strongly reduced (to 0-10%) currents produced by KCNQ1-4 subunits expressed individually and also those produced by KCNQ2+KCNQ3 and KCNQ1+KCNE1 heteromers, which are thought to generate neuronal M-currents (I sub(K,M)) and cardiac slow delayed rectifier currents (I sub(K,s)), respectively. * The activity of KCNQ2+KCNQ3, KCNQ2 and KCNQ3 channels recorded with cell-attached pipettes was strongly and reversibly reduced by Oxo-M applied to the extra-patch membrane. * It is concluded that M sub(1) receptors couple to all known KCNQ subunits and that inhibition of KCNQ2+KCNQ3 channels, like that of native M-channels, requires a diffusible second messenger. |
doi_str_mv | 10.1111/j.1469-7793.2000.t01-2-00349.x |
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Hadley, J K ; Wood, I C ; Abogadie, F C ; Jentsch, T J ; Brown, DA</creator><creatorcontrib>Selyanko, A A ; Hadley, J K ; Wood, I C ; Abogadie, F C ; Jentsch, T J ; Brown, DA</creatorcontrib><description>* KCNQ1-4 potassium channels were expressed in mammalian Chinese hamster ovary (CHO) cells stably transfected with M sub(1) muscarinic acetylcholine receptors and currents were recorded using the whole-cell perforated patch technique and cell-attached patch recording. * Stimulation of M sub(1) receptors by 10 mu m oxotremorine-M (Oxo-M) strongly reduced (to 0-10%) currents produced by KCNQ1-4 subunits expressed individually and also those produced by KCNQ2+KCNQ3 and KCNQ1+KCNE1 heteromers, which are thought to generate neuronal M-currents (I sub(K,M)) and cardiac slow delayed rectifier currents (I sub(K,s)), respectively. * The activity of KCNQ2+KCNQ3, KCNQ2 and KCNQ3 channels recorded with cell-attached pipettes was strongly and reversibly reduced by Oxo-M applied to the extra-patch membrane. * It is concluded that M sub(1) receptors couple to all known KCNQ subunits and that inhibition of KCNQ2+KCNQ3 channels, like that of native M-channels, requires a diffusible second messenger.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1111/j.1469-7793.2000.t01-2-00349.x</identifier><language>eng</language><ispartof>The Journal of physiology, 2000-02, Vol.522 (3), p.349-355</ispartof><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></links><search><creatorcontrib>Selyanko, A A</creatorcontrib><creatorcontrib>Hadley, J K</creatorcontrib><creatorcontrib>Wood, I C</creatorcontrib><creatorcontrib>Abogadie, F C</creatorcontrib><creatorcontrib>Jentsch, T J</creatorcontrib><creatorcontrib>Brown, DA</creatorcontrib><title>Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M sub(1) muscarinic acetylcholine receptors</title><title>The Journal of physiology</title><description>* KCNQ1-4 potassium channels were expressed in mammalian Chinese hamster ovary (CHO) cells stably transfected with M sub(1) muscarinic acetylcholine receptors and currents were recorded using the whole-cell perforated patch technique and cell-attached patch recording. * Stimulation of M sub(1) receptors by 10 mu m oxotremorine-M (Oxo-M) strongly reduced (to 0-10%) currents produced by KCNQ1-4 subunits expressed individually and also those produced by KCNQ2+KCNQ3 and KCNQ1+KCNE1 heteromers, which are thought to generate neuronal M-currents (I sub(K,M)) and cardiac slow delayed rectifier currents (I sub(K,s)), respectively. * The activity of KCNQ2+KCNQ3, KCNQ2 and KCNQ3 channels recorded with cell-attached pipettes was strongly and reversibly reduced by Oxo-M applied to the extra-patch membrane. * It is concluded that M sub(1) receptors couple to all known KCNQ subunits and that inhibition of KCNQ2+KCNQ3 channels, like that of native M-channels, requires a diffusible second messenger.</description><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqVj0tLxDAUhYMoWB__4a5kXKTeNK2160FxEAXB_ZCJd2iGPGpvIuO_dwRx79mcxfdx4AhxpbBWh9zsatXeDrLvB103iFhnVLKRiLod6v2RqP7wsagQm0bqvlOn4ox5h6g0DkMlyiqObuOySxHSFp6WL69KtjClbJhdCWBHEyN5BtpPMzHTO7gIwYRgvDMRLPkD_HQGnoHLZqGuIRS2ZnbRWTCW8pe3Y_IuEsxkacpp5gtxsjWe6fK3z8Xi4f5t-SinOX0U4rwOjn-WTaRUeK367q45vOm0_of6DWTVWbo</recordid><startdate>20000201</startdate><enddate>20000201</enddate><creator>Selyanko, A A</creator><creator>Hadley, J K</creator><creator>Wood, I C</creator><creator>Abogadie, F C</creator><creator>Jentsch, T J</creator><creator>Brown, DA</creator><scope>7TK</scope></search><sort><creationdate>20000201</creationdate><title>Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M sub(1) muscarinic acetylcholine receptors</title><author>Selyanko, A A ; Hadley, J K ; Wood, I C ; Abogadie, F C ; Jentsch, T J ; Brown, DA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_17582469533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Selyanko, A A</creatorcontrib><creatorcontrib>Hadley, J K</creatorcontrib><creatorcontrib>Wood, I C</creatorcontrib><creatorcontrib>Abogadie, F C</creatorcontrib><creatorcontrib>Jentsch, T J</creatorcontrib><creatorcontrib>Brown, DA</creatorcontrib><collection>Neurosciences Abstracts</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Selyanko, A A</au><au>Hadley, J K</au><au>Wood, I C</au><au>Abogadie, F C</au><au>Jentsch, T J</au><au>Brown, DA</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M sub(1) muscarinic acetylcholine receptors</atitle><jtitle>The Journal of physiology</jtitle><date>2000-02-01</date><risdate>2000</risdate><volume>522</volume><issue>3</issue><spage>349</spage><epage>355</epage><pages>349-355</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>* KCNQ1-4 potassium channels were expressed in mammalian Chinese hamster ovary (CHO) cells stably transfected with M sub(1) muscarinic acetylcholine receptors and currents were recorded using the whole-cell perforated patch technique and cell-attached patch recording. * Stimulation of M sub(1) receptors by 10 mu m oxotremorine-M (Oxo-M) strongly reduced (to 0-10%) currents produced by KCNQ1-4 subunits expressed individually and also those produced by KCNQ2+KCNQ3 and KCNQ1+KCNE1 heteromers, which are thought to generate neuronal M-currents (I sub(K,M)) and cardiac slow delayed rectifier currents (I sub(K,s)), respectively. * The activity of KCNQ2+KCNQ3, KCNQ2 and KCNQ3 channels recorded with cell-attached pipettes was strongly and reversibly reduced by Oxo-M applied to the extra-patch membrane. * It is concluded that M sub(1) receptors couple to all known KCNQ subunits and that inhibition of KCNQ2+KCNQ3 channels, like that of native M-channels, requires a diffusible second messenger.</abstract><doi>10.1111/j.1469-7793.2000.t01-2-00349.x</doi></addata></record> |
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title | Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M sub(1) muscarinic acetylcholine receptors |
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