Contractile function assessment by intraventricular balloon alters the ability of regional ischaemia to evoke ventricular fibrillation

Background and purpose In drug research using the rat Langendorff heart preparation, it is possible to study left ventricular (LV) contractility using an intraventricular balloon (IVB), and arrhythmogenesis during coronary ligation‐induced regional ischaemia. Assessing both concurrently would halve...

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Veröffentlicht in:British journal of pharmacology 2016-01, Vol.173 (1), p.39-52
Hauptverfasser: Wilder, Catherine D E, Masoud, Radwa, Yazar, Duygu, O'Brien, Brett A, Eykyn, Thomas R, Curtis, Michael J
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container_issue 1
container_start_page 39
container_title British journal of pharmacology
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creator Wilder, Catherine D E
Masoud, Radwa
Yazar, Duygu
O'Brien, Brett A
Eykyn, Thomas R
Curtis, Michael J
description Background and purpose In drug research using the rat Langendorff heart preparation, it is possible to study left ventricular (LV) contractility using an intraventricular balloon (IVB), and arrhythmogenesis during coronary ligation‐induced regional ischaemia. Assessing both concurrently would halve animal requirements. We aimed to test the validity of this approach. Experimental approach The electrocardiogram (ECG) and LV function (IVB) were recorded during regional ischaemia of different extents in a randomized and blinded study. Key results IVB‐induced proarrhythmia was anticipated, but in hearts with an ischaemic zone (IZ) made deliberately small, an inflated IVB reduced ischaemia‐induced ventricular fibrillation (VF) incidence as a trend. Repeating studies in hearts with large IZs revealed the effect to be significant. There were no changes in QT interval or other variables that might explain the effect. Insertion of an IVB that was minimally inflated had no effect on any variable compared with ‘no IVB’ controls. The antiarrhythmic effect of verapamil (a positive control drug) was unaffected by IVB inflation. Removal of an inflated (but not a non‐inflated) IVB caused a release of lactate commensurate with reperfusion of an endocardial/subendocardial layer of IVB‐induced ischaemia. This was confirmed by intracellular 31phosphorus (31P) nuclear magnetic resonance (NMR) spectroscopy. Conclusions and implications IVB inflation does not inhibit VF suppression by a standard drug, but it has profound antiarrhythmic effects of its own, likely to be due to inflation‐induced localized ischaemia. This means rhythm and contractility cannot be assessed concurrently by this approach, with implications for drug discovery and safety assessment.
doi_str_mv 10.1111/bph.13332
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Assessing both concurrently would halve animal requirements. We aimed to test the validity of this approach. Experimental approach The electrocardiogram (ECG) and LV function (IVB) were recorded during regional ischaemia of different extents in a randomized and blinded study. Key results IVB‐induced proarrhythmia was anticipated, but in hearts with an ischaemic zone (IZ) made deliberately small, an inflated IVB reduced ischaemia‐induced ventricular fibrillation (VF) incidence as a trend. Repeating studies in hearts with large IZs revealed the effect to be significant. There were no changes in QT interval or other variables that might explain the effect. Insertion of an IVB that was minimally inflated had no effect on any variable compared with ‘no IVB’ controls. The antiarrhythmic effect of verapamil (a positive control drug) was unaffected by IVB inflation. Removal of an inflated (but not a non‐inflated) IVB caused a release of lactate commensurate with reperfusion of an endocardial/subendocardial layer of IVB‐induced ischaemia. This was confirmed by intracellular 31phosphorus (31P) nuclear magnetic resonance (NMR) spectroscopy. Conclusions and implications IVB inflation does not inhibit VF suppression by a standard drug, but it has profound antiarrhythmic effects of its own, likely to be due to inflation‐induced localized ischaemia. This means rhythm and contractility cannot be assessed concurrently by this approach, with implications for drug discovery and safety assessment.</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1111/bph.13332</identifier><identifier>PMID: 26377788</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Animals ; Cardiac arrhythmia ; Cardiac Catheters ; Electrocardiography ; Lactic Acid - metabolism ; Magnetic Resonance Spectroscopy ; Male ; Myocardial Contraction ; Myocardial Ischemia - pathology ; Myocardial Ischemia - physiopathology ; NMR ; Nuclear magnetic resonance ; Phosphorus - metabolism ; Rats ; Research Paper ; Research Papers ; Ventricular Fibrillation - drug therapy ; Ventricular Fibrillation - physiopathology ; Ventricular Function, Left ; Verapamil - therapeutic use</subject><ispartof>British journal of pharmacology, 2016-01, Vol.173 (1), p.39-52</ispartof><rights>2015 The British Pharmacological Society</rights><rights>2015 The British Pharmacological Society.</rights><rights>2016 The British Pharmacological Society</rights><rights>2015 The British Pharmacological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4432-67ad7fe49ea62c94b77ac15536ca0ce5b493b4c327299d8a8f1765a766ca03db3</citedby><cites>FETCH-LOGICAL-c4432-67ad7fe49ea62c94b77ac15536ca0ce5b493b4c327299d8a8f1765a766ca03db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4813384/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4813384/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,1414,1430,27907,27908,45557,45558,46392,46816,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26377788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilder, Catherine D E</creatorcontrib><creatorcontrib>Masoud, Radwa</creatorcontrib><creatorcontrib>Yazar, Duygu</creatorcontrib><creatorcontrib>O'Brien, Brett A</creatorcontrib><creatorcontrib>Eykyn, Thomas R</creatorcontrib><creatorcontrib>Curtis, Michael J</creatorcontrib><title>Contractile function assessment by intraventricular balloon alters the ability of regional ischaemia to evoke ventricular fibrillation</title><title>British journal of pharmacology</title><addtitle>Br J Pharmacol</addtitle><description>Background and purpose In drug research using the rat Langendorff heart preparation, it is possible to study left ventricular (LV) contractility using an intraventricular balloon (IVB), and arrhythmogenesis during coronary ligation‐induced regional ischaemia. Assessing both concurrently would halve animal requirements. We aimed to test the validity of this approach. Experimental approach The electrocardiogram (ECG) and LV function (IVB) were recorded during regional ischaemia of different extents in a randomized and blinded study. Key results IVB‐induced proarrhythmia was anticipated, but in hearts with an ischaemic zone (IZ) made deliberately small, an inflated IVB reduced ischaemia‐induced ventricular fibrillation (VF) incidence as a trend. Repeating studies in hearts with large IZs revealed the effect to be significant. There were no changes in QT interval or other variables that might explain the effect. Insertion of an IVB that was minimally inflated had no effect on any variable compared with ‘no IVB’ controls. The antiarrhythmic effect of verapamil (a positive control drug) was unaffected by IVB inflation. Removal of an inflated (but not a non‐inflated) IVB caused a release of lactate commensurate with reperfusion of an endocardial/subendocardial layer of IVB‐induced ischaemia. This was confirmed by intracellular 31phosphorus (31P) nuclear magnetic resonance (NMR) spectroscopy. Conclusions and implications IVB inflation does not inhibit VF suppression by a standard drug, but it has profound antiarrhythmic effects of its own, likely to be due to inflation‐induced localized ischaemia. This means rhythm and contractility cannot be assessed concurrently by this approach, with implications for drug discovery and safety assessment.</description><subject>Animals</subject><subject>Cardiac arrhythmia</subject><subject>Cardiac Catheters</subject><subject>Electrocardiography</subject><subject>Lactic Acid - metabolism</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Male</subject><subject>Myocardial Contraction</subject><subject>Myocardial Ischemia - pathology</subject><subject>Myocardial Ischemia - physiopathology</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Phosphorus - metabolism</subject><subject>Rats</subject><subject>Research Paper</subject><subject>Research Papers</subject><subject>Ventricular Fibrillation - drug therapy</subject><subject>Ventricular Fibrillation - physiopathology</subject><subject>Ventricular Function, Left</subject><subject>Verapamil - therapeutic use</subject><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFvFCEUx4nR2LV68AsYEi96mBYGZmAuJrpRa9JED3omD_ZNl8oMK8ys2S_g55bp1qaayAXI--XHe_wJec7ZGS_r3O62Z1wIUT8gKy5VWzVC84dkxRhTFedan5AnOV8zVoqqeUxO6lYopbRekV_rOE4J3OQD0n4eyyGOFHLGnAccJ2oP1C_EvlySd3OARC2EEBcsTJgynbZIwfrgpwONPU14VRwQqM9uCzh4oFOkuI_fkd639N4mHwIsLz4lj3oIGZ_d7qfk24f3X9cX1eXnj5_Wby8rJ6Woq1bBRvUoO4S2dp20SoHjTSNaB8xhY2UnrHSiVnXXbTTonqu2AdUudbGx4pS8OXp3sx1w45Z2IJhd8gOkg4ngzd-V0W_NVdwbqcsHa1kEr24FKf6YMU9mKGNiGWPEOGfDVcN5J4XWBX35D3od51Q-5oZiomVlpkK9PlIuxZwT9nfNcGaWdE1J19ykW9gX97u_I__EWYDzI_CzxHn4v8m8-3JxVP4GkqizAQ</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Wilder, Catherine D E</creator><creator>Masoud, Radwa</creator><creator>Yazar, Duygu</creator><creator>O'Brien, Brett A</creator><creator>Eykyn, Thomas R</creator><creator>Curtis, Michael J</creator><general>Blackwell Publishing Ltd</general><general>John Wiley and Sons Inc</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>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201601</creationdate><title>Contractile function assessment by intraventricular balloon alters the ability of regional ischaemia to evoke ventricular fibrillation</title><author>Wilder, Catherine D E ; 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Assessing both concurrently would halve animal requirements. We aimed to test the validity of this approach. Experimental approach The electrocardiogram (ECG) and LV function (IVB) were recorded during regional ischaemia of different extents in a randomized and blinded study. Key results IVB‐induced proarrhythmia was anticipated, but in hearts with an ischaemic zone (IZ) made deliberately small, an inflated IVB reduced ischaemia‐induced ventricular fibrillation (VF) incidence as a trend. Repeating studies in hearts with large IZs revealed the effect to be significant. There were no changes in QT interval or other variables that might explain the effect. Insertion of an IVB that was minimally inflated had no effect on any variable compared with ‘no IVB’ controls. The antiarrhythmic effect of verapamil (a positive control drug) was unaffected by IVB inflation. Removal of an inflated (but not a non‐inflated) IVB caused a release of lactate commensurate with reperfusion of an endocardial/subendocardial layer of IVB‐induced ischaemia. This was confirmed by intracellular 31phosphorus (31P) nuclear magnetic resonance (NMR) spectroscopy. Conclusions and implications IVB inflation does not inhibit VF suppression by a standard drug, but it has profound antiarrhythmic effects of its own, likely to be due to inflation‐induced localized ischaemia. This means rhythm and contractility cannot be assessed concurrently by this approach, with implications for drug discovery and safety assessment.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26377788</pmid><doi>10.1111/bph.13332</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; PubMed Central; Alma/SFX Local Collection
subjects Animals
Cardiac arrhythmia
Cardiac Catheters
Electrocardiography
Lactic Acid - metabolism
Magnetic Resonance Spectroscopy
Male
Myocardial Contraction
Myocardial Ischemia - pathology
Myocardial Ischemia - physiopathology
NMR
Nuclear magnetic resonance
Phosphorus - metabolism
Rats
Research Paper
Research Papers
Ventricular Fibrillation - drug therapy
Ventricular Fibrillation - physiopathology
Ventricular Function, Left
Verapamil - therapeutic use
title Contractile function assessment by intraventricular balloon alters the ability of regional ischaemia to evoke ventricular fibrillation
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