Chloroform is a potent activator of cardiac and neuronal Kir3 channels
Chloroform has been used over decades in anesthesia before it was replaced by other volatile anesthetics like halothane or sevoflurane. Some of the reasons were inadmissible side effects of chloroform like bradycardia or neural illness. In the present study, we identified members of the G protein-ac...
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description | Chloroform has been used over decades in anesthesia before it was replaced by other volatile anesthetics like halothane or sevoflurane. Some of the reasons were inadmissible side effects of chloroform like bradycardia or neural illness. In the present study, we identified members of the G protein-activated inwardly rectifying potassium channel family (Kir3) expressed in
Xenopus
oocytes as potential common molecular targets for both the neural and cardiac effects of chloroform. Millimolar concentration currents representing a 1:10000 dilution of commercially available chloroform were used in laboratories that augment neuronal Kir3.1/3.2 currents as well as cardiac Kir3.1/3.4. This effect was selective and only observed in currents from Kir3 subunits but not in currents from Kir2 subunits. Augmentation of atrial Kir3.1/3.4 currents leads to an effective drop of the heart rate and a reduction in contraction force in isolated mouse atria. |
doi_str_mv | 10.1007/s00210-019-01751-x |
format | Article |
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Xenopus
oocytes as potential common molecular targets for both the neural and cardiac effects of chloroform. Millimolar concentration currents representing a 1:10000 dilution of commercially available chloroform were used in laboratories that augment neuronal Kir3.1/3.2 currents as well as cardiac Kir3.1/3.4. This effect was selective and only observed in currents from Kir3 subunits but not in currents from Kir2 subunits. Augmentation of atrial Kir3.1/3.4 currents leads to an effective drop of the heart rate and a reduction in contraction force in isolated mouse atria.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/s00210-019-01751-x</identifier><identifier>PMID: 31720798</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anesthesia ; Anesthetics ; Animals ; Atrial Function - drug effects ; Biomedical and Life Sciences ; Biomedicine ; Bradycardia ; Bradycardia - chemically induced ; Bradycardia - physiopathology ; Chloroform ; Chloroform - toxicity ; Contraction ; G Protein-Coupled Inwardly-Rectifying Potassium Channels - physiology ; Halothane ; Heart Atria - drug effects ; Heart rate ; HEK293 Cells ; Humans ; Mice ; Neurons - drug effects ; Neurons - physiology ; Neurosciences ; Oocytes ; Original Article ; Pharmacology/Toxicology ; Potassium channels (inwardly-rectifying) ; Sevoflurane ; Xenopus laevis</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 2020-04, Vol.393 (4), p.573-580</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2019</rights><rights>Naunyn-Schmiedeberg's Archives of Pharmacology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-85aff2b1408bd64f51d11c4256ef4ad0f477add3d6e3e28639693b1fd7b6c3263</citedby><cites>FETCH-LOGICAL-c375t-85aff2b1408bd64f51d11c4256ef4ad0f477add3d6e3e28639693b1fd7b6c3263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00210-019-01751-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00210-019-01751-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31720798$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kollert, Sina</creatorcontrib><creatorcontrib>Döring, Frank</creatorcontrib><creatorcontrib>Gergs, Ulrich</creatorcontrib><creatorcontrib>Wischmeyer, Erhard</creatorcontrib><title>Chloroform is a potent activator of cardiac and neuronal Kir3 channels</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn-Schmiedeberg's Arch Pharmacol</addtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>Chloroform has been used over decades in anesthesia before it was replaced by other volatile anesthetics like halothane or sevoflurane. Some of the reasons were inadmissible side effects of chloroform like bradycardia or neural illness. In the present study, we identified members of the G protein-activated inwardly rectifying potassium channel family (Kir3) expressed in
Xenopus
oocytes as potential common molecular targets for both the neural and cardiac effects of chloroform. Millimolar concentration currents representing a 1:10000 dilution of commercially available chloroform were used in laboratories that augment neuronal Kir3.1/3.2 currents as well as cardiac Kir3.1/3.4. This effect was selective and only observed in currents from Kir3 subunits but not in currents from Kir2 subunits. Augmentation of atrial Kir3.1/3.4 currents leads to an effective drop of the heart rate and a reduction in contraction force in isolated mouse atria.</description><subject>Anesthesia</subject><subject>Anesthetics</subject><subject>Animals</subject><subject>Atrial Function - drug effects</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bradycardia</subject><subject>Bradycardia - chemically induced</subject><subject>Bradycardia - physiopathology</subject><subject>Chloroform</subject><subject>Chloroform - toxicity</subject><subject>Contraction</subject><subject>G Protein-Coupled Inwardly-Rectifying Potassium Channels - physiology</subject><subject>Halothane</subject><subject>Heart Atria - drug effects</subject><subject>Heart rate</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Mice</subject><subject>Neurons - drug effects</subject><subject>Neurons - physiology</subject><subject>Neurosciences</subject><subject>Oocytes</subject><subject>Original Article</subject><subject>Pharmacology/Toxicology</subject><subject>Potassium channels (inwardly-rectifying)</subject><subject>Sevoflurane</subject><subject>Xenopus laevis</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kD1PwzAQhi0EoqXwBxiQJeaAz47tZEQVBUQlFpgtJ7ZpqjQudoLKv8eQAhvD6YZ7P04PQudAroAQeR0JoUAyAmUaySHbHaAp5IxmUAI9RNN0LzKgZTFBJzGuCSECOD9GEwaSElkWU7SYr1ofvPNhg5uINd763nY91nXfvOveB-wdrnUwja6x7gzu7BB8p1v82ASG65XuOtvGU3TkdBvt2X7P0Mvi9nl-ny2f7h7mN8usZpL3WcG1c7SCnBSVEbnjYADqnHJhXa4NcbmU2hhmhGWWFoKVomQVOCMrUTMq2Axdjrnb4N8GG3u19kNI70RFU4PgBeEsqeioqoOPMVintqHZ6PChgKgvdGpEpxI69Y1O7ZLpYh89VBtrfi0_rJKAjYKYTt2rDX_d_8R-AntKeRQ</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Kollert, Sina</creator><creator>Döring, Frank</creator><creator>Gergs, Ulrich</creator><creator>Wischmeyer, Erhard</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20200401</creationdate><title>Chloroform is a potent activator of cardiac and neuronal Kir3 channels</title><author>Kollert, Sina ; 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Some of the reasons were inadmissible side effects of chloroform like bradycardia or neural illness. In the present study, we identified members of the G protein-activated inwardly rectifying potassium channel family (Kir3) expressed in
Xenopus
oocytes as potential common molecular targets for both the neural and cardiac effects of chloroform. Millimolar concentration currents representing a 1:10000 dilution of commercially available chloroform were used in laboratories that augment neuronal Kir3.1/3.2 currents as well as cardiac Kir3.1/3.4. This effect was selective and only observed in currents from Kir3 subunits but not in currents from Kir2 subunits. Augmentation of atrial Kir3.1/3.4 currents leads to an effective drop of the heart rate and a reduction in contraction force in isolated mouse atria.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>31720798</pmid><doi>10.1007/s00210-019-01751-x</doi><tpages>8</tpages></addata></record> |
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subjects | Anesthesia Anesthetics Animals Atrial Function - drug effects Biomedical and Life Sciences Biomedicine Bradycardia Bradycardia - chemically induced Bradycardia - physiopathology Chloroform Chloroform - toxicity Contraction G Protein-Coupled Inwardly-Rectifying Potassium Channels - physiology Halothane Heart Atria - drug effects Heart rate HEK293 Cells Humans Mice Neurons - drug effects Neurons - physiology Neurosciences Oocytes Original Article Pharmacology/Toxicology Potassium channels (inwardly-rectifying) Sevoflurane Xenopus laevis |
title | Chloroform is a potent activator of cardiac and neuronal Kir3 channels |
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