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Intravenous lipid emulsion prolongs survival in rats intoxicated with digoxin
Abstract Background Intravenous lipid emulsion eliminates the toxicity related symptoms for several drugs. We hypothesized that intravenous lipid emulsion prolongs the survival time in digoxin-intoxicated rats. Methods Electrocardiograms of 14 anesthesized Wistar rats were monitored. All of the rats...
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Published in: | The American journal of emergency medicine 2016-06, Vol.34 (6), p.1112-1116 |
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creator | Yurtlu, Bülent Serhan, M.D Özbilgin, Şule, M.D Yurtlu, Derya Arslan, M.D Boztaş, Nilay, M.D Kamacı, Gonca, D.V.M Akaltun, Mahmut Hancı, Volkan, M.D Yılmaz, Osman, PhD |
description | Abstract Background Intravenous lipid emulsion eliminates the toxicity related symptoms for several drugs. We hypothesized that intravenous lipid emulsion prolongs the survival time in digoxin-intoxicated rats. Methods Electrocardiograms of 14 anesthesized Wistar rats were monitored. All of the rats received digoxin infusion at a rate of 12 ml/h (0.25 mg/ml). Five minutes after the start of digoxin infusion, animals were treated either with 12.4 ml/kg intravenous lipid emulsion (Group L) or saline (Group C). The primary outcome variable was time elapsed until asystole development. Cumulative dose of digoxin required to induce asystole was also recorded. Results Mean time until asystole development in Groups C and L were 21.28 ± 8.61 min and 32.00 ± 5.41 min, respectively (p < 0.05). The mean lethal doses of digoxin in the Groups C and L were 3.97 ± 1.54 mg/kg, and 6.09 ± 0.96 mg/kg, respectively (p < 0.05). Conclusion Intravenous lipid emulsion prolonged the time until asystole development and cumulative lethal dose in rats intoxicated with digoxin. |
doi_str_mv | 10.1016/j.ajem.2016.03.038 |
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We hypothesized that intravenous lipid emulsion prolongs the survival time in digoxin-intoxicated rats. Methods Electrocardiograms of 14 anesthesized Wistar rats were monitored. All of the rats received digoxin infusion at a rate of 12 ml/h (0.25 mg/ml). Five minutes after the start of digoxin infusion, animals were treated either with 12.4 ml/kg intravenous lipid emulsion (Group L) or saline (Group C). The primary outcome variable was time elapsed until asystole development. Cumulative dose of digoxin required to induce asystole was also recorded. Results Mean time until asystole development in Groups C and L were 21.28 ± 8.61 min and 32.00 ± 5.41 min, respectively (p < 0.05). The mean lethal doses of digoxin in the Groups C and L were 3.97 ± 1.54 mg/kg, and 6.09 ± 0.96 mg/kg, respectively (p < 0.05). Conclusion Intravenous lipid emulsion prolonged the time until asystole development and cumulative lethal dose in rats intoxicated with digoxin.</description><identifier>ISSN: 0735-6757</identifier><identifier>EISSN: 1532-8171</identifier><identifier>DOI: 10.1016/j.ajem.2016.03.038</identifier><identifier>PMID: 27073138</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Arrhythmia Agents - toxicity ; Digoxin - toxicity ; Dose-Response Relationship, Drug ; Drug dosages ; Emergency ; Emergency medical care ; Emulsions ; Fat Emulsions, Intravenous - therapeutic use ; Heart Arrest - etiology ; Heart Arrest - prevention & control ; Heart rate ; Hypotheses ; Infusions, Intravenous ; Intensive care ; Laboratory animals ; Lipids ; Medical research ; Mortality ; Rats ; Rats, Wistar ; Rodents ; Studies ; Ventilation</subject><ispartof>The American journal of emergency medicine, 2016-06, Vol.34 (6), p.1112-1116</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-591f84d6d961a31eed6ea8d413e92a07b69b4476daae334178fda7ba171ccbe43</citedby><cites>FETCH-LOGICAL-c472t-591f84d6d961a31eed6ea8d413e92a07b69b4476daae334178fda7ba171ccbe43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27073138$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yurtlu, Bülent Serhan, M.D</creatorcontrib><creatorcontrib>Özbilgin, Şule, M.D</creatorcontrib><creatorcontrib>Yurtlu, Derya Arslan, M.D</creatorcontrib><creatorcontrib>Boztaş, Nilay, M.D</creatorcontrib><creatorcontrib>Kamacı, Gonca, D.V.M</creatorcontrib><creatorcontrib>Akaltun, Mahmut</creatorcontrib><creatorcontrib>Hancı, Volkan, M.D</creatorcontrib><creatorcontrib>Yılmaz, Osman, PhD</creatorcontrib><title>Intravenous lipid emulsion prolongs survival in rats intoxicated with digoxin</title><title>The American journal of emergency medicine</title><addtitle>Am J Emerg Med</addtitle><description>Abstract Background Intravenous lipid emulsion eliminates the toxicity related symptoms for several drugs. We hypothesized that intravenous lipid emulsion prolongs the survival time in digoxin-intoxicated rats. Methods Electrocardiograms of 14 anesthesized Wistar rats were monitored. All of the rats received digoxin infusion at a rate of 12 ml/h (0.25 mg/ml). Five minutes after the start of digoxin infusion, animals were treated either with 12.4 ml/kg intravenous lipid emulsion (Group L) or saline (Group C). The primary outcome variable was time elapsed until asystole development. Cumulative dose of digoxin required to induce asystole was also recorded. Results Mean time until asystole development in Groups C and L were 21.28 ± 8.61 min and 32.00 ± 5.41 min, respectively (p < 0.05). The mean lethal doses of digoxin in the Groups C and L were 3.97 ± 1.54 mg/kg, and 6.09 ± 0.96 mg/kg, respectively (p < 0.05). Conclusion Intravenous lipid emulsion prolonged the time until asystole development and cumulative lethal dose in rats intoxicated with digoxin.</description><subject>Animals</subject><subject>Anti-Arrhythmia Agents - toxicity</subject><subject>Digoxin - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug dosages</subject><subject>Emergency</subject><subject>Emergency medical care</subject><subject>Emulsions</subject><subject>Fat Emulsions, Intravenous - therapeutic use</subject><subject>Heart Arrest - etiology</subject><subject>Heart Arrest - prevention & control</subject><subject>Heart rate</subject><subject>Hypotheses</subject><subject>Infusions, Intravenous</subject><subject>Intensive care</subject><subject>Laboratory animals</subject><subject>Lipids</subject><subject>Medical research</subject><subject>Mortality</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rodents</subject><subject>Studies</subject><subject>Ventilation</subject><issn>0735-6757</issn><issn>1532-8171</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkkFrFTEQx4Mo9rX6BTzIghcv-8wk2SQLIpSitVDxoJ5DNplXs-5mn8nu0357s7yq0IMIAxOS3wzzz38IeQZ0CxTkq35rexy3rJy3lJfQD8gGGs5qDQoekg1VvKmlatQJOc25pxRANOIxOWGqPAHXG_LhKs7JHjBOS66GsA--wnEZcphitU_TMMWbXOUlHcLBDlWIVbJzLnmefgZnZ_TVjzB_rXy4KRfxCXm0s0PGp3f5jHx59_bzxfv6-uPl1cX5de2EYnPdtLDTwkvfSrAcEL1Eq70Aji2zVHWy7YRQ0luLnAtQeuet6mxR5VyHgp-Rl8e-ZcTvC-bZjCE7HAYbsQgxoKmWDLT4D1S1jVYSWlbQF_fQflpSLEJWSgFtQEOh2JFyaco54c7sUxhtujVAzeqL6c3qi1l9MZSX0KXo-V3rpRvR_yn5bUQBXh8BLN92CJhMdgGjQx8Sutn4Kfy7_5t75W4IsTg0fMNbzH91mMwMNZ_WzVgXAySlTDDBfwEfcLNP</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Yurtlu, Bülent Serhan, M.D</creator><creator>Özbilgin, Şule, M.D</creator><creator>Yurtlu, Derya Arslan, M.D</creator><creator>Boztaş, Nilay, M.D</creator><creator>Kamacı, Gonca, D.V.M</creator><creator>Akaltun, Mahmut</creator><creator>Hancı, Volkan, M.D</creator><creator>Yılmaz, Osman, PhD</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20160601</creationdate><title>Intravenous lipid emulsion prolongs survival in rats intoxicated with digoxin</title><author>Yurtlu, Bülent Serhan, M.D ; Özbilgin, Şule, M.D ; Yurtlu, Derya Arslan, M.D ; Boztaş, Nilay, M.D ; Kamacı, Gonca, D.V.M ; Akaltun, Mahmut ; Hancı, Volkan, M.D ; Yılmaz, Osman, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-591f84d6d961a31eed6ea8d413e92a07b69b4476daae334178fda7ba171ccbe43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Anti-Arrhythmia Agents - toxicity</topic><topic>Digoxin - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug dosages</topic><topic>Emergency</topic><topic>Emergency medical care</topic><topic>Emulsions</topic><topic>Fat Emulsions, Intravenous - therapeutic use</topic><topic>Heart Arrest - etiology</topic><topic>Heart Arrest - prevention & control</topic><topic>Heart rate</topic><topic>Hypotheses</topic><topic>Infusions, Intravenous</topic><topic>Intensive care</topic><topic>Laboratory animals</topic><topic>Lipids</topic><topic>Medical research</topic><topic>Mortality</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Rodents</topic><topic>Studies</topic><topic>Ventilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yurtlu, Bülent Serhan, M.D</creatorcontrib><creatorcontrib>Özbilgin, Şule, M.D</creatorcontrib><creatorcontrib>Yurtlu, Derya Arslan, M.D</creatorcontrib><creatorcontrib>Boztaş, Nilay, M.D</creatorcontrib><creatorcontrib>Kamacı, Gonca, D.V.M</creatorcontrib><creatorcontrib>Akaltun, Mahmut</creatorcontrib><creatorcontrib>Hancı, Volkan, M.D</creatorcontrib><creatorcontrib>Yılmaz, Osman, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Immunology Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>The American journal of emergency medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yurtlu, Bülent Serhan, M.D</au><au>Özbilgin, Şule, M.D</au><au>Yurtlu, Derya Arslan, M.D</au><au>Boztaş, Nilay, M.D</au><au>Kamacı, Gonca, D.V.M</au><au>Akaltun, Mahmut</au><au>Hancı, Volkan, M.D</au><au>Yılmaz, Osman, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravenous lipid emulsion prolongs survival in rats intoxicated with digoxin</atitle><jtitle>The American journal of emergency medicine</jtitle><addtitle>Am J Emerg Med</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>34</volume><issue>6</issue><spage>1112</spage><epage>1116</epage><pages>1112-1116</pages><issn>0735-6757</issn><eissn>1532-8171</eissn><abstract>Abstract Background Intravenous lipid emulsion eliminates the toxicity related symptoms for several drugs. We hypothesized that intravenous lipid emulsion prolongs the survival time in digoxin-intoxicated rats. Methods Electrocardiograms of 14 anesthesized Wistar rats were monitored. All of the rats received digoxin infusion at a rate of 12 ml/h (0.25 mg/ml). Five minutes after the start of digoxin infusion, animals were treated either with 12.4 ml/kg intravenous lipid emulsion (Group L) or saline (Group C). The primary outcome variable was time elapsed until asystole development. Cumulative dose of digoxin required to induce asystole was also recorded. Results Mean time until asystole development in Groups C and L were 21.28 ± 8.61 min and 32.00 ± 5.41 min, respectively (p < 0.05). The mean lethal doses of digoxin in the Groups C and L were 3.97 ± 1.54 mg/kg, and 6.09 ± 0.96 mg/kg, respectively (p < 0.05). Conclusion Intravenous lipid emulsion prolonged the time until asystole development and cumulative lethal dose in rats intoxicated with digoxin.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27073138</pmid><doi>10.1016/j.ajem.2016.03.038</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Anti-Arrhythmia Agents - toxicity Digoxin - toxicity Dose-Response Relationship, Drug Drug dosages Emergency Emergency medical care Emulsions Fat Emulsions, Intravenous - therapeutic use Heart Arrest - etiology Heart Arrest - prevention & control Heart rate Hypotheses Infusions, Intravenous Intensive care Laboratory animals Lipids Medical research Mortality Rats Rats, Wistar Rodents Studies Ventilation |
title | Intravenous lipid emulsion prolongs survival in rats intoxicated with digoxin |
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