Tissue-Level Cardiac Electrophysiology Studied in Murine Myocardium Using a Microelectrode Array: Autonomic and Thermal Modulation
Cardiac electrophysiology is regulated by the autonomic nervous system, and this has both pathophysiological, and possibly therapeutic importance. Furthermore, chamber differences in electrophysiology exist between atria and ventricles, yet there have been few direct comparisons. There is substantia...
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description | Cardiac electrophysiology is regulated by the autonomic nervous system, and this has both pathophysiological, and possibly therapeutic importance. Furthermore, chamber differences in electrophysiology exist between atria and ventricles, yet there have been few direct comparisons. There is substantial literature on ion channel modulation at the single-cell level but less work on how this affects tissue-level parameters. We used a microelectrode array system to explore these issues using murine atrial and ventricular tissue slices. Activation time, conduction velocity and repolarisation were measured, and their modulation by temperature and pharmacological autonomic agonists were assessed. The system recorded reliable measurements under control conditions in the absence of drug/thermal challenge, and significant baseline differences were found in chamber electrophysiology. The sodium channel blocker mexiletine, produced large magnitude changes in all three measured parameters. Carbachol and isoprenaline induced differing effects in atria and ventricles, whereas temperature produced similar effects on activation and repolarisation. |
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Furthermore, chamber differences in electrophysiology exist between atria and ventricles, yet there have been few direct comparisons. There is substantial literature on ion channel modulation at the single-cell level but less work on how this affects tissue-level parameters. We used a microelectrode array system to explore these issues using murine atrial and ventricular tissue slices. Activation time, conduction velocity and repolarisation were measured, and their modulation by temperature and pharmacological autonomic agonists were assessed. The system recorded reliable measurements under control conditions in the absence of drug/thermal challenge, and significant baseline differences were found in chamber electrophysiology. The sodium channel blocker mexiletine, produced large magnitude changes in all three measured parameters. Carbachol and isoprenaline induced differing effects in atria and ventricles, whereas temperature produced similar effects on activation and repolarisation.</description><identifier>ISSN: 0022-2631</identifier><identifier>EISSN: 1432-1424</identifier><identifier>DOI: 10.1007/s00232-017-9973-y</identifier><identifier>PMID: 28766006</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Activation ; Animals ; Atria ; Atrial Function - drug effects ; Atrial Function - physiology ; Autonomic nervous system ; Biochemistry ; Biomedical and Life Sciences ; Carbachol ; Carbachol - pharmacology ; Conduction ; Electrophysiologic Techniques, Cardiac ; Electrophysiological Phenomena ; Electrophysiology ; Female ; Heart ; Heart Atria ; Heart diseases ; Heart Ventricles ; Human Physiology ; Ion channels ; Isoproterenol - pharmacology ; Life Sciences ; Male ; Mexiletine - pharmacology ; Mice ; Microelectrodes ; Modulation ; Myocardium ; Pharmacology ; Sodium ; Temperature ; Velocity ; Ventricle ; Ventricular Function - drug effects ; Ventricular Function - physiology</subject><ispartof>The Journal of membrane biology, 2017-10, Vol.250 (5), p.471-481</ispartof><rights>The Author(s) 2017</rights><rights>The Journal of Membrane Biology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-78cb015dfb9f9f126961507e1dc78745e14c35a8df2b56513313b399a9b7dc9e3</citedby><cites>FETCH-LOGICAL-c470t-78cb015dfb9f9f126961507e1dc78745e14c35a8df2b56513313b399a9b7dc9e3</cites><orcidid>0000-0001-7703-4151</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00232-017-9973-y$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00232-017-9973-y$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,315,781,785,886,27929,27930,41493,42562,51324</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28766006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lane, Jem D.</creatorcontrib><creatorcontrib>Montaigne, David</creatorcontrib><creatorcontrib>Tinker, Andrew</creatorcontrib><title>Tissue-Level Cardiac Electrophysiology Studied in Murine Myocardium Using a Microelectrode Array: Autonomic and Thermal Modulation</title><title>The Journal of membrane biology</title><addtitle>J Membrane Biol</addtitle><addtitle>J Membr Biol</addtitle><description>Cardiac electrophysiology is regulated by the autonomic nervous system, and this has both pathophysiological, and possibly therapeutic importance. Furthermore, chamber differences in electrophysiology exist between atria and ventricles, yet there have been few direct comparisons. There is substantial literature on ion channel modulation at the single-cell level but less work on how this affects tissue-level parameters. We used a microelectrode array system to explore these issues using murine atrial and ventricular tissue slices. Activation time, conduction velocity and repolarisation were measured, and their modulation by temperature and pharmacological autonomic agonists were assessed. The system recorded reliable measurements under control conditions in the absence of drug/thermal challenge, and significant baseline differences were found in chamber electrophysiology. The sodium channel blocker mexiletine, produced large magnitude changes in all three measured parameters. Carbachol and isoprenaline induced differing effects in atria and ventricles, whereas temperature produced similar effects on activation and repolarisation.</description><subject>Activation</subject><subject>Animals</subject><subject>Atria</subject><subject>Atrial Function - drug effects</subject><subject>Atrial Function - physiology</subject><subject>Autonomic nervous system</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Carbachol</subject><subject>Carbachol - pharmacology</subject><subject>Conduction</subject><subject>Electrophysiologic Techniques, Cardiac</subject><subject>Electrophysiological Phenomena</subject><subject>Electrophysiology</subject><subject>Female</subject><subject>Heart</subject><subject>Heart Atria</subject><subject>Heart diseases</subject><subject>Heart Ventricles</subject><subject>Human Physiology</subject><subject>Ion channels</subject><subject>Isoproterenol - pharmacology</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mexiletine - pharmacology</subject><subject>Mice</subject><subject>Microelectrodes</subject><subject>Modulation</subject><subject>Myocardium</subject><subject>Pharmacology</subject><subject>Sodium</subject><subject>Temperature</subject><subject>Velocity</subject><subject>Ventricle</subject><subject>Ventricular Function - drug effects</subject><subject>Ventricular Function - physiology</subject><issn>0022-2631</issn><issn>1432-1424</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kUGP0zAQhSMEYrsLP4ALssSFS8BjJ3bDAamqlgWpFQe6Z8uxJ61XiV3sZKVc-eW46rJakDhZ8vve84xfUbwB-gEolR8TpYyzkoIsm0bycn5WLKDKN1Cx6nmxyDIrmeBwUVymdEczKEX1srhgSykEpWJR_Nq5lCYsN3iPPVnraJ025LpHM8ZwPMzJhT7sZ_JjnKxDS5wn2yk6j2Q7B3PCp4HcJuf3RJOtMzHg2WuRrGLU8yeymsbgw-AM0d6S3QHjoHuyDXbq9eiCf1W86HSf8PXDeVXcfrnerb-Wm-8339arTWkqScdSLk1LobZd23RNB0w0AmoqEayRS1nVCJXhtV7ajrW1qIFz4C1vGt200poG-VXx-Zx7nNoBrUE_Rt2rY3SDjrMK2qm_Fe8Oah_uVS2AUwk54P1DQAw_J0yjGlwy2PfaY5iSgobVNYAEltF3_6B3YYo-r5epimWqEnWm4Ezlb0spYvc4DFB1alidG1a5OHVqWM3Z8_bpFo-OP5VmgJ2BlCW_x_jk6f-m_gaZALP_</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Lane, Jem D.</creator><creator>Montaigne, David</creator><creator>Tinker, Andrew</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7703-4151</orcidid></search><sort><creationdate>20171001</creationdate><title>Tissue-Level Cardiac Electrophysiology Studied in Murine Myocardium Using a Microelectrode Array: Autonomic and Thermal Modulation</title><author>Lane, Jem D. ; Montaigne, David ; Tinker, Andrew</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-78cb015dfb9f9f126961507e1dc78745e14c35a8df2b56513313b399a9b7dc9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Activation</topic><topic>Animals</topic><topic>Atria</topic><topic>Atrial Function - drug effects</topic><topic>Atrial Function - physiology</topic><topic>Autonomic nervous system</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Carbachol</topic><topic>Carbachol - pharmacology</topic><topic>Conduction</topic><topic>Electrophysiologic Techniques, Cardiac</topic><topic>Electrophysiological Phenomena</topic><topic>Electrophysiology</topic><topic>Female</topic><topic>Heart</topic><topic>Heart Atria</topic><topic>Heart diseases</topic><topic>Heart Ventricles</topic><topic>Human Physiology</topic><topic>Ion channels</topic><topic>Isoproterenol - pharmacology</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Mexiletine - pharmacology</topic><topic>Mice</topic><topic>Microelectrodes</topic><topic>Modulation</topic><topic>Myocardium</topic><topic>Pharmacology</topic><topic>Sodium</topic><topic>Temperature</topic><topic>Velocity</topic><topic>Ventricle</topic><topic>Ventricular Function - drug effects</topic><topic>Ventricular Function - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of membrane biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lane, Jem D.</au><au>Montaigne, David</au><au>Tinker, Andrew</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue-Level Cardiac Electrophysiology Studied in Murine Myocardium Using a Microelectrode Array: Autonomic and Thermal Modulation</atitle><jtitle>The Journal of membrane biology</jtitle><stitle>J Membrane Biol</stitle><addtitle>J Membr Biol</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>250</volume><issue>5</issue><spage>471</spage><epage>481</epage><pages>471-481</pages><issn>0022-2631</issn><eissn>1432-1424</eissn><abstract>Cardiac electrophysiology is regulated by the autonomic nervous system, and this has both pathophysiological, and possibly therapeutic importance. Furthermore, chamber differences in electrophysiology exist between atria and ventricles, yet there have been few direct comparisons. There is substantial literature on ion channel modulation at the single-cell level but less work on how this affects tissue-level parameters. We used a microelectrode array system to explore these issues using murine atrial and ventricular tissue slices. Activation time, conduction velocity and repolarisation were measured, and their modulation by temperature and pharmacological autonomic agonists were assessed. The system recorded reliable measurements under control conditions in the absence of drug/thermal challenge, and significant baseline differences were found in chamber electrophysiology. The sodium channel blocker mexiletine, produced large magnitude changes in all three measured parameters. Carbachol and isoprenaline induced differing effects in atria and ventricles, whereas temperature produced similar effects on activation and repolarisation.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28766006</pmid><doi>10.1007/s00232-017-9973-y</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7703-4151</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Activation Animals Atria Atrial Function - drug effects Atrial Function - physiology Autonomic nervous system Biochemistry Biomedical and Life Sciences Carbachol Carbachol - pharmacology Conduction Electrophysiologic Techniques, Cardiac Electrophysiological Phenomena Electrophysiology Female Heart Heart Atria Heart diseases Heart Ventricles Human Physiology Ion channels Isoproterenol - pharmacology Life Sciences Male Mexiletine - pharmacology Mice Microelectrodes Modulation Myocardium Pharmacology Sodium Temperature Velocity Ventricle Ventricular Function - drug effects Ventricular Function - physiology |
title | Tissue-Level Cardiac Electrophysiology Studied in Murine Myocardium Using a Microelectrode Array: Autonomic and Thermal Modulation |
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