Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution
The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear. We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillat...
Gespeichert in:
Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 2002-10, Vol.106 (14), p.1859-1866 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1866 |
---|---|
container_issue | 14 |
container_start_page | 1859 |
container_title | Circulation (New York, N.Y.) |
container_volume | 106 |
creator | WU, Tsu-Juey LIN, Shien-Fong WEISS, James N TING, Chih-Tai CHEN, Peng-Sheng |
description | The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear.
We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF.
Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. Both excitability and APD restitution are important in VF maintenance. |
doi_str_mv | 10.1161/01.CIR.0000031334.49170.FB |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_212676059</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>209249711</sourcerecordid><originalsourceid>FETCH-LOGICAL-c415t-2d07f5a783421f327845abd4b6b88dc5807de56605ae7a9b0edbf817892aa0b83</originalsourceid><addsrcrecordid>eNpFUd1q2zAUFmOjTbu-whCFXdrTr2X3bg3NGigMRnctjiyZqTiWJ8nb8gB97ylNIOKAdDjfDzofQreU1JQ29Auh9Xr7oyaHwynnohYdVaTe3L9DKyqZqITk3Xu0KvOuUpyxS3SV0ktpG67kBbqkjMumEWyFXp__Bpz3s0s4DPiPm3L0_TJCxIM30Y8jZB8m7EulUBpncQRjfMa_HMSc7vB2N4eYYerdQcH9630G40ef9xgmi6F_E5hDLtoeRmyXeNSMLmWfl8P7I_owwJjczem-Rj83D8_rx-rp-7ft-utT1Qsqc8UsUYME1XLB6MCZaoUEY4VpTNvaXrZEWVc-RiQ4BZ0hzpqhpartGAAxLb9Gt0fdOYbfS_HXL2GJU7HUjLJGFWZXQHdHUB9DStENeo5-B3GvKdGHADShugSgzwHotwD05r6QP50cFrNz9kw9bbwAPp8AkHoYh1g259MZxzvZMSX5fxmbkdM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>212676059</pqid></control><display><type>article</type><title>Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution</title><source>MEDLINE</source><source>American Heart Association Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Journals@Ovid Complete</source><creator>WU, Tsu-Juey ; LIN, Shien-Fong ; WEISS, James N ; TING, Chih-Tai ; CHEN, Peng-Sheng</creator><creatorcontrib>WU, Tsu-Juey ; LIN, Shien-Fong ; WEISS, James N ; TING, Chih-Tai ; CHEN, Peng-Sheng</creatorcontrib><description>The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear.
We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF.
Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. Both excitability and APD restitution are important in VF maintenance.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/01.CIR.0000031334.49170.FB</identifier><identifier>PMID: 12356642</identifier><identifier>CODEN: CIRCAZ</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Action Potentials - drug effects ; Action Potentials - physiology ; Animals ; Biological and medical sciences ; Body Surface Potential Mapping ; Calcium Channel Blockers - pharmacology ; Cardiac dysrhythmias ; Cardiac Pacing, Artificial ; Cardiology. Vascular system ; Dose-Response Relationship, Drug ; Electrocardiography - drug effects ; Electrocardiography - methods ; Electrodes, Implanted ; Electrophysiologic Techniques, Cardiac ; Fluorescent Dyes ; Fourier Analysis ; Gallopamil - pharmacology ; Heart ; Heart - drug effects ; Heart - physiopathology ; In Vitro Techniques ; Light ; Medical sciences ; Optics and Photonics ; Pyridinium Compounds ; Rabbits ; Sodium Channel Blockers - pharmacology ; Tachycardia, Ventricular - drug therapy ; Tachycardia, Ventricular - physiopathology ; Tetrodotoxin - pharmacology ; Time Factors ; Ventricular Fibrillation - classification ; Ventricular Fibrillation - drug therapy ; Ventricular Fibrillation - physiopathology</subject><ispartof>Circulation (New York, N.Y.), 2002-10, Vol.106 (14), p.1859-1866</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Oct 1, 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-2d07f5a783421f327845abd4b6b88dc5807de56605ae7a9b0edbf817892aa0b83</citedby><cites>FETCH-LOGICAL-c415t-2d07f5a783421f327845abd4b6b88dc5807de56605ae7a9b0edbf817892aa0b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13959275$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12356642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WU, Tsu-Juey</creatorcontrib><creatorcontrib>LIN, Shien-Fong</creatorcontrib><creatorcontrib>WEISS, James N</creatorcontrib><creatorcontrib>TING, Chih-Tai</creatorcontrib><creatorcontrib>CHEN, Peng-Sheng</creatorcontrib><title>Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear.
We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF.
Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. Both excitability and APD restitution are important in VF maintenance.</description><subject>Action Potentials - drug effects</subject><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Surface Potential Mapping</subject><subject>Calcium Channel Blockers - pharmacology</subject><subject>Cardiac dysrhythmias</subject><subject>Cardiac Pacing, Artificial</subject><subject>Cardiology. Vascular system</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electrocardiography - drug effects</subject><subject>Electrocardiography - methods</subject><subject>Electrodes, Implanted</subject><subject>Electrophysiologic Techniques, Cardiac</subject><subject>Fluorescent Dyes</subject><subject>Fourier Analysis</subject><subject>Gallopamil - pharmacology</subject><subject>Heart</subject><subject>Heart - drug effects</subject><subject>Heart - physiopathology</subject><subject>In Vitro Techniques</subject><subject>Light</subject><subject>Medical sciences</subject><subject>Optics and Photonics</subject><subject>Pyridinium Compounds</subject><subject>Rabbits</subject><subject>Sodium Channel Blockers - pharmacology</subject><subject>Tachycardia, Ventricular - drug therapy</subject><subject>Tachycardia, Ventricular - physiopathology</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Time Factors</subject><subject>Ventricular Fibrillation - classification</subject><subject>Ventricular Fibrillation - drug therapy</subject><subject>Ventricular Fibrillation - physiopathology</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUd1q2zAUFmOjTbu-whCFXdrTr2X3bg3NGigMRnctjiyZqTiWJ8nb8gB97ylNIOKAdDjfDzofQreU1JQ29Auh9Xr7oyaHwynnohYdVaTe3L9DKyqZqITk3Xu0KvOuUpyxS3SV0ktpG67kBbqkjMumEWyFXp__Bpz3s0s4DPiPm3L0_TJCxIM30Y8jZB8m7EulUBpncQRjfMa_HMSc7vB2N4eYYerdQcH9630G40ef9xgmi6F_E5hDLtoeRmyXeNSMLmWfl8P7I_owwJjczem-Rj83D8_rx-rp-7ft-utT1Qsqc8UsUYME1XLB6MCZaoUEY4VpTNvaXrZEWVc-RiQ4BZ0hzpqhpartGAAxLb9Gt0fdOYbfS_HXL2GJU7HUjLJGFWZXQHdHUB9DStENeo5-B3GvKdGHADShugSgzwHotwD05r6QP50cFrNz9kw9bbwAPp8AkHoYh1g259MZxzvZMSX5fxmbkdM</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>WU, Tsu-Juey</creator><creator>LIN, Shien-Fong</creator><creator>WEISS, James N</creator><creator>TING, Chih-Tai</creator><creator>CHEN, Peng-Sheng</creator><general>Lippincott Williams & Wilkins</general><general>American Heart Association, Inc</general><scope>IQODW</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>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope></search><sort><creationdate>20021001</creationdate><title>Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution</title><author>WU, Tsu-Juey ; LIN, Shien-Fong ; WEISS, James N ; TING, Chih-Tai ; CHEN, Peng-Sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-2d07f5a783421f327845abd4b6b88dc5807de56605ae7a9b0edbf817892aa0b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Action Potentials - drug effects</topic><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Surface Potential Mapping</topic><topic>Calcium Channel Blockers - pharmacology</topic><topic>Cardiac dysrhythmias</topic><topic>Cardiac Pacing, Artificial</topic><topic>Cardiology. Vascular system</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electrocardiography - drug effects</topic><topic>Electrocardiography - methods</topic><topic>Electrodes, Implanted</topic><topic>Electrophysiologic Techniques, Cardiac</topic><topic>Fluorescent Dyes</topic><topic>Fourier Analysis</topic><topic>Gallopamil - pharmacology</topic><topic>Heart</topic><topic>Heart - drug effects</topic><topic>Heart - physiopathology</topic><topic>In Vitro Techniques</topic><topic>Light</topic><topic>Medical sciences</topic><topic>Optics and Photonics</topic><topic>Pyridinium Compounds</topic><topic>Rabbits</topic><topic>Sodium Channel Blockers - pharmacology</topic><topic>Tachycardia, Ventricular - drug therapy</topic><topic>Tachycardia, Ventricular - physiopathology</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Time Factors</topic><topic>Ventricular Fibrillation - classification</topic><topic>Ventricular Fibrillation - drug therapy</topic><topic>Ventricular Fibrillation - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WU, Tsu-Juey</creatorcontrib><creatorcontrib>LIN, Shien-Fong</creatorcontrib><creatorcontrib>WEISS, James N</creatorcontrib><creatorcontrib>TING, Chih-Tai</creatorcontrib><creatorcontrib>CHEN, Peng-Sheng</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WU, Tsu-Juey</au><au>LIN, Shien-Fong</au><au>WEISS, James N</au><au>TING, Chih-Tai</au><au>CHEN, Peng-Sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>106</volume><issue>14</issue><spage>1859</spage><epage>1866</epage><pages>1859-1866</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><coden>CIRCAZ</coden><abstract>The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear.
We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF.
Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. Both excitability and APD restitution are important in VF maintenance.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>12356642</pmid><doi>10.1161/01.CIR.0000031334.49170.FB</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-7322 |
ispartof | Circulation (New York, N.Y.), 2002-10, Vol.106 (14), p.1859-1866 |
issn | 0009-7322 1524-4539 |
language | eng |
recordid | cdi_proquest_journals_212676059 |
source | MEDLINE; American Heart Association Journals; EZB-FREE-00999 freely available EZB journals; Journals@Ovid Complete |
subjects | Action Potentials - drug effects Action Potentials - physiology Animals Biological and medical sciences Body Surface Potential Mapping Calcium Channel Blockers - pharmacology Cardiac dysrhythmias Cardiac Pacing, Artificial Cardiology. Vascular system Dose-Response Relationship, Drug Electrocardiography - drug effects Electrocardiography - methods Electrodes, Implanted Electrophysiologic Techniques, Cardiac Fluorescent Dyes Fourier Analysis Gallopamil - pharmacology Heart Heart - drug effects Heart - physiopathology In Vitro Techniques Light Medical sciences Optics and Photonics Pyridinium Compounds Rabbits Sodium Channel Blockers - pharmacology Tachycardia, Ventricular - drug therapy Tachycardia, Ventricular - physiopathology Tetrodotoxin - pharmacology Time Factors Ventricular Fibrillation - classification Ventricular Fibrillation - drug therapy Ventricular Fibrillation - physiopathology |
title | Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T13%3A10%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Two%20types%20of%20ventricular%20fibrillation%20in%20isolated%20rabbit%20hearts:%20Importance%20of%20excitability%20and%20action%20potential%20duration%20restitution&rft.jtitle=Circulation%20(New%20York,%20N.Y.)&rft.au=WU,%20Tsu-Juey&rft.date=2002-10-01&rft.volume=106&rft.issue=14&rft.spage=1859&rft.epage=1866&rft.pages=1859-1866&rft.issn=0009-7322&rft.eissn=1524-4539&rft.coden=CIRCAZ&rft_id=info:doi/10.1161/01.CIR.0000031334.49170.FB&rft_dat=%3Cproquest_cross%3E209249711%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=212676059&rft_id=info:pmid/12356642&rfr_iscdi=true |