Severity of the cardiac impairment determines whether digitalis prolongs or reduces survival of rats with heart failure due to myocardial infarction
Abstract Background The aim of the present study was to evaluate if the influence of digitalis on survival depends on the severity of cardiac dysfunction in heart failure (HF). Methods and results Doppler echocardiogram (DE) parameters were analyzed in 84 Wistar control (C) and 80 Wistar rats treate...
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Veröffentlicht in: | International journal of cardiology 2013-07, Vol.167 (2), p.357-361 |
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description | Abstract Background The aim of the present study was to evaluate if the influence of digitalis on survival depends on the severity of cardiac dysfunction in heart failure (HF). Methods and results Doppler echocardiogram (DE) parameters were analyzed in 84 Wistar control (C) and 80 Wistar rats treated with 0.1 mg/100 g/day of digitoxin (D) five days after coronary occlusion. The DE variables correlated with the survival of the animals were: myocardial infarction size, left chamber dimensions, fractional area change and E/A ratio. The animals were observed for up to 280 days. Mortality was worsened in rats in the D group with a myocardial infarction (MI) < 37% and with better DE predictors of survival. Digitoxin was found to prolong survival in rats with an MI ≥ 37% and worse DE predictors. Conclusion For the first time our study has shown experimentally that the action of digitalis glycosides can positively or negatively influence survival during treatment of HF. It prolongs survival of those in advanced state and compromises survival when there is less severity of the disease. In fact, the greater benefits occur when digitoxin was used in heightened ventricular dilatations and worse ventricular performance. |
doi_str_mv | 10.1016/j.ijcard.2011.12.097 |
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Methods and results Doppler echocardiogram (DE) parameters were analyzed in 84 Wistar control (C) and 80 Wistar rats treated with 0.1 mg/100 g/day of digitoxin (D) five days after coronary occlusion. The DE variables correlated with the survival of the animals were: myocardial infarction size, left chamber dimensions, fractional area change and E/A ratio. The animals were observed for up to 280 days. Mortality was worsened in rats in the D group with a myocardial infarction (MI) < 37% and with better DE predictors of survival. Digitoxin was found to prolong survival in rats with an MI ≥ 37% and worse DE predictors. Conclusion For the first time our study has shown experimentally that the action of digitalis glycosides can positively or negatively influence survival during treatment of HF. It prolongs survival of those in advanced state and compromises survival when there is less severity of the disease. In fact, the greater benefits occur when digitoxin was used in heightened ventricular dilatations and worse ventricular performance.</description><identifier>ISSN: 0167-5273</identifier><identifier>EISSN: 1874-1754</identifier><identifier>DOI: 10.1016/j.ijcard.2011.12.097</identifier><identifier>PMID: 22285448</identifier><identifier>CODEN: IJCDD5</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Animals ; Biological and medical sciences ; Cardiology. Vascular system ; Cardiovascular ; Coronary heart disease ; Digitalis ; Digitoxin - therapeutic use ; Female ; Heart ; Heart failure ; Heart Failure - drug therapy ; Heart Failure - mortality ; Heart Failure - pathology ; Heart failure, cardiogenic pulmonary edema, cardiac enlargement ; Medical sciences ; Myocardial infarction ; Myocardial Infarction - drug therapy ; Myocardial Infarction - mortality ; Myocardial Infarction - pathology ; Myocarditis. Cardiomyopathies ; Rats ; Rats, Wistar ; Severity of Illness Index ; Survival ; Survival Rate - trends</subject><ispartof>International journal of cardiology, 2013-07, Vol.167 (2), p.357-361</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-a31693943e2579540e995b9a75caa5966de889bcb165d5f814da3e48ff4db6ef3</citedby><cites>FETCH-LOGICAL-c493t-a31693943e2579540e995b9a75caa5966de889bcb165d5f814da3e48ff4db6ef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijcard.2011.12.097$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27468702$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22285448$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>dos Santos, Alexandra A</creatorcontrib><creatorcontrib>Helber, Izo</creatorcontrib><creatorcontrib>Antonio, Ednei L</creatorcontrib><creatorcontrib>Franco, Marcelo F</creatorcontrib><creatorcontrib>Tucci, Paulo J.F</creatorcontrib><title>Severity of the cardiac impairment determines whether digitalis prolongs or reduces survival of rats with heart failure due to myocardial infarction</title><title>International journal of cardiology</title><addtitle>Int J Cardiol</addtitle><description>Abstract Background The aim of the present study was to evaluate if the influence of digitalis on survival depends on the severity of cardiac dysfunction in heart failure (HF). Methods and results Doppler echocardiogram (DE) parameters were analyzed in 84 Wistar control (C) and 80 Wistar rats treated with 0.1 mg/100 g/day of digitoxin (D) five days after coronary occlusion. The DE variables correlated with the survival of the animals were: myocardial infarction size, left chamber dimensions, fractional area change and E/A ratio. The animals were observed for up to 280 days. Mortality was worsened in rats in the D group with a myocardial infarction (MI) < 37% and with better DE predictors of survival. Digitoxin was found to prolong survival in rats with an MI ≥ 37% and worse DE predictors. Conclusion For the first time our study has shown experimentally that the action of digitalis glycosides can positively or negatively influence survival during treatment of HF. It prolongs survival of those in advanced state and compromises survival when there is less severity of the disease. In fact, the greater benefits occur when digitoxin was used in heightened ventricular dilatations and worse ventricular performance.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Coronary heart disease</subject><subject>Digitalis</subject><subject>Digitoxin - therapeutic use</subject><subject>Female</subject><subject>Heart</subject><subject>Heart failure</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - mortality</subject><subject>Heart Failure - pathology</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>Medical sciences</subject><subject>Myocardial infarction</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Myocardial Infarction - mortality</subject><subject>Myocardial Infarction - pathology</subject><subject>Myocarditis. Cardiomyopathies</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Severity of Illness Index</subject><subject>Survival</subject><subject>Survival Rate - trends</subject><issn>0167-5273</issn><issn>1874-1754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks2O1DAQhCMEYoeFN0DIFyQuM9iO8-MLElrxJ63EYeFsOXZnp0MSD21n0LwHD4yjGUDiwsmXr6raXV0UzwXfCS7q18MOB2fJ7yQXYifkjuvmQbERbaO2oqnUw2KTsWZbyaa8Kp7EOHDOldbt4-JKStlWSrWb4ucdHIEwnVjoWdoDWy3ROobTwSJNMCfmIQFNOENkP_aQIWIe7zHZESM7UBjDfB9ZIEbgF5epuNARj3ZcPcmmLMO0Z3uwlFhvcVwImF-ApcCmUzgnjgzn3pJLGOanxaPejhGeXd7r4uv7d19uPm5vP3_4dPP2duuULtPWlqLWpVYlyKrRleKgddVp21TO2krXtYe21Z3rRF35qm-F8rYE1fa98l0NfXldvDr75k98XyAmM2F0MI52hrBEI8pay1IpXmdUnVFHIUaC3hwIJ0snI7hZ-zCDOfdh1j6MkCb3kWUvLglLN4H_I_pdQAZeXgAbnR17srPD-JdrVN02XGbuzZmDvI8jApnoEGYHHglcMj7g_yb518CNOGPO_AYniENYaM67NsLELDB36-2spyMEl7JpdfkLqIzDPg</recordid><startdate>20130731</startdate><enddate>20130731</enddate><creator>dos Santos, Alexandra A</creator><creator>Helber, Izo</creator><creator>Antonio, Ednei L</creator><creator>Franco, Marcelo F</creator><creator>Tucci, Paulo J.F</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>20130731</creationdate><title>Severity of the cardiac impairment determines whether digitalis prolongs or reduces survival of rats with heart failure due to myocardial infarction</title><author>dos Santos, Alexandra A ; Helber, Izo ; Antonio, Ednei L ; Franco, Marcelo F ; Tucci, Paulo J.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-a31693943e2579540e995b9a75caa5966de889bcb165d5f814da3e48ff4db6ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular</topic><topic>Coronary heart disease</topic><topic>Digitalis</topic><topic>Digitoxin - therapeutic use</topic><topic>Female</topic><topic>Heart</topic><topic>Heart failure</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - mortality</topic><topic>Heart Failure - pathology</topic><topic>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</topic><topic>Medical sciences</topic><topic>Myocardial infarction</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Myocardial Infarction - mortality</topic><topic>Myocardial Infarction - pathology</topic><topic>Myocarditis. Cardiomyopathies</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Severity of Illness Index</topic><topic>Survival</topic><topic>Survival Rate - trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>dos Santos, Alexandra A</creatorcontrib><creatorcontrib>Helber, Izo</creatorcontrib><creatorcontrib>Antonio, Ednei L</creatorcontrib><creatorcontrib>Franco, Marcelo F</creatorcontrib><creatorcontrib>Tucci, Paulo J.F</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>MEDLINE - Academic</collection><jtitle>International journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>dos Santos, Alexandra A</au><au>Helber, Izo</au><au>Antonio, Ednei L</au><au>Franco, Marcelo F</au><au>Tucci, Paulo J.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Severity of the cardiac impairment determines whether digitalis prolongs or reduces survival of rats with heart failure due to myocardial infarction</atitle><jtitle>International journal of cardiology</jtitle><addtitle>Int J Cardiol</addtitle><date>2013-07-31</date><risdate>2013</risdate><volume>167</volume><issue>2</issue><spage>357</spage><epage>361</epage><pages>357-361</pages><issn>0167-5273</issn><eissn>1874-1754</eissn><coden>IJCDD5</coden><abstract>Abstract Background The aim of the present study was to evaluate if the influence of digitalis on survival depends on the severity of cardiac dysfunction in heart failure (HF). Methods and results Doppler echocardiogram (DE) parameters were analyzed in 84 Wistar control (C) and 80 Wistar rats treated with 0.1 mg/100 g/day of digitoxin (D) five days after coronary occlusion. The DE variables correlated with the survival of the animals were: myocardial infarction size, left chamber dimensions, fractional area change and E/A ratio. The animals were observed for up to 280 days. Mortality was worsened in rats in the D group with a myocardial infarction (MI) < 37% and with better DE predictors of survival. Digitoxin was found to prolong survival in rats with an MI ≥ 37% and worse DE predictors. Conclusion For the first time our study has shown experimentally that the action of digitalis glycosides can positively or negatively influence survival during treatment of HF. It prolongs survival of those in advanced state and compromises survival when there is less severity of the disease. In fact, the greater benefits occur when digitoxin was used in heightened ventricular dilatations and worse ventricular performance.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>22285448</pmid><doi>10.1016/j.ijcard.2011.12.097</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Cardiology. Vascular system Cardiovascular Coronary heart disease Digitalis Digitoxin - therapeutic use Female Heart Heart failure Heart Failure - drug therapy Heart Failure - mortality Heart Failure - pathology Heart failure, cardiogenic pulmonary edema, cardiac enlargement Medical sciences Myocardial infarction Myocardial Infarction - drug therapy Myocardial Infarction - mortality Myocardial Infarction - pathology Myocarditis. Cardiomyopathies Rats Rats, Wistar Severity of Illness Index Survival Survival Rate - trends |
title | Severity of the cardiac impairment determines whether digitalis prolongs or reduces survival of rats with heart failure due to myocardial infarction |
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