Treatment of haemodynamic and electrocardiographic side-effects resulting from imipramine toxicity in rats and dogs
This study was designed to analyze the effects of carbocromene and dipyridamole on the haemodynamic and electrocardiographic side-effects resulting from imipramine infusion in anaesthetised rats and dogs. Imipramine was infused at 1 mg/kg/min until cardiac failure and vascular collapse terminated th...
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Veröffentlicht in: | Naunyn-Schmiedeberg's archives of pharmacology 1985-08, Vol.330 (2), p.155-161 |
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description | This study was designed to analyze the effects of carbocromene and dipyridamole on the haemodynamic and electrocardiographic side-effects resulting from imipramine infusion in anaesthetised rats and dogs. Imipramine was infused at 1 mg/kg/min until cardiac failure and vascular collapse terminated the experiment at 21 +/- 2.3 min in rats and at 29.5 +/- 2.1 min in dogs. This was characterized by hypotension, bradycardia, intraventricular conduction delay, cardiac tachyarrhythmia and A-V block. Carbocromene (4 mg/kg i.v., followed by 80 micrograms/kg/min) protected the animals against heart failure. This was associated with delayed hypotension and negative inotropy, and lower incidence of heart block. Survival time increased to 37 +/- 1.5 min (P less than 0.05), and 54.2 +/- 2.6 min (P less than 0.02) in rats and dogs, respectively. Dipyridamole (0.5 mg/kg i.v., followed by 80 micrograms/kg/min) failed to decrease imipramine toxicity as judged by the haemodynamic and electrocardiographic parameters and did not alter survival time of imipramine controls. These results suggest that carbocromene is an effective treatment for imipramine-induced cardiovascular collapse and cardiac arrhythmias, the beneficial effects being largely due to metabolic and membrane stabilizing effects. Carbocromene has both therapeutic and prophylactic value and appears to be superior to dipyridamole therapy. |
doi_str_mv | 10.1007/BF00499909 |
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B ; KETTENBACH, B ; GÖBEL, H ; NITZ, R.-E</creator><creatorcontrib>FIEDLER, V. B ; KETTENBACH, B ; GÖBEL, H ; NITZ, R.-E</creatorcontrib><description>This study was designed to analyze the effects of carbocromene and dipyridamole on the haemodynamic and electrocardiographic side-effects resulting from imipramine infusion in anaesthetised rats and dogs. Imipramine was infused at 1 mg/kg/min until cardiac failure and vascular collapse terminated the experiment at 21 +/- 2.3 min in rats and at 29.5 +/- 2.1 min in dogs. This was characterized by hypotension, bradycardia, intraventricular conduction delay, cardiac tachyarrhythmia and A-V block. Carbocromene (4 mg/kg i.v., followed by 80 micrograms/kg/min) protected the animals against heart failure. This was associated with delayed hypotension and negative inotropy, and lower incidence of heart block. Survival time increased to 37 +/- 1.5 min (P less than 0.05), and 54.2 +/- 2.6 min (P less than 0.02) in rats and dogs, respectively. Dipyridamole (0.5 mg/kg i.v., followed by 80 micrograms/kg/min) failed to decrease imipramine toxicity as judged by the haemodynamic and electrocardiographic parameters and did not alter survival time of imipramine controls. These results suggest that carbocromene is an effective treatment for imipramine-induced cardiovascular collapse and cardiac arrhythmias, the beneficial effects being largely due to metabolic and membrane stabilizing effects. Carbocromene has both therapeutic and prophylactic value and appears to be superior to dipyridamole therapy.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/BF00499909</identifier><identifier>PMID: 4047178</identifier><identifier>CODEN: NSAPCC</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Animals ; Arrhythmias, Cardiac - chemically induced ; Arrhythmias, Cardiac - prevention & control ; Biological and medical sciences ; Chromonar - pharmacology ; Coumarins - pharmacology ; Dipyridamole - pharmacology ; Dogs ; Drug toxicity and drugs side effects treatment ; Electrocardiography ; Female ; Heart Failure - chemically induced ; Heart Failure - prevention & control ; Hemodynamics - drug effects ; Imipramine - antagonists & inhibitors ; Imipramine - poisoning ; Male ; Medical sciences ; Pharmacology. Drug treatments ; Rats ; Toxicity: cardiovascular system</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 1985-08, Vol.330 (2), p.155-161</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c226t-4e059091d5a98e562769dcd2712f89b0f38b7653af05156a36c1a35327795aea3</citedby><cites>FETCH-LOGICAL-c226t-4e059091d5a98e562769dcd2712f89b0f38b7653af05156a36c1a35327795aea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8696090$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4047178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FIEDLER, V. B</creatorcontrib><creatorcontrib>KETTENBACH, B</creatorcontrib><creatorcontrib>GÖBEL, H</creatorcontrib><creatorcontrib>NITZ, R.-E</creatorcontrib><title>Treatment of haemodynamic and electrocardiographic side-effects resulting from imipramine toxicity in rats and dogs</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>This study was designed to analyze the effects of carbocromene and dipyridamole on the haemodynamic and electrocardiographic side-effects resulting from imipramine infusion in anaesthetised rats and dogs. Imipramine was infused at 1 mg/kg/min until cardiac failure and vascular collapse terminated the experiment at 21 +/- 2.3 min in rats and at 29.5 +/- 2.1 min in dogs. This was characterized by hypotension, bradycardia, intraventricular conduction delay, cardiac tachyarrhythmia and A-V block. Carbocromene (4 mg/kg i.v., followed by 80 micrograms/kg/min) protected the animals against heart failure. This was associated with delayed hypotension and negative inotropy, and lower incidence of heart block. Survival time increased to 37 +/- 1.5 min (P less than 0.05), and 54.2 +/- 2.6 min (P less than 0.02) in rats and dogs, respectively. Dipyridamole (0.5 mg/kg i.v., followed by 80 micrograms/kg/min) failed to decrease imipramine toxicity as judged by the haemodynamic and electrocardiographic parameters and did not alter survival time of imipramine controls. These results suggest that carbocromene is an effective treatment for imipramine-induced cardiovascular collapse and cardiac arrhythmias, the beneficial effects being largely due to metabolic and membrane stabilizing effects. Carbocromene has both therapeutic and prophylactic value and appears to be superior to dipyridamole therapy.</description><subject>Animals</subject><subject>Arrhythmias, Cardiac - chemically induced</subject><subject>Arrhythmias, Cardiac - prevention & control</subject><subject>Biological and medical sciences</subject><subject>Chromonar - pharmacology</subject><subject>Coumarins - pharmacology</subject><subject>Dipyridamole - pharmacology</subject><subject>Dogs</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Heart Failure - chemically induced</subject><subject>Heart Failure - prevention & control</subject><subject>Hemodynamics - drug effects</subject><subject>Imipramine - antagonists & inhibitors</subject><subject>Imipramine - poisoning</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pharmacology. 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B</creator><creator>KETTENBACH, B</creator><creator>GÖBEL, H</creator><creator>NITZ, R.-E</creator><general>Springer</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></search><sort><creationdate>198508</creationdate><title>Treatment of haemodynamic and electrocardiographic side-effects resulting from imipramine toxicity in rats and dogs</title><author>FIEDLER, V. B ; KETTENBACH, B ; GÖBEL, H ; NITZ, R.-E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c226t-4e059091d5a98e562769dcd2712f89b0f38b7653af05156a36c1a35327795aea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Arrhythmias, Cardiac - chemically induced</topic><topic>Arrhythmias, Cardiac - prevention & control</topic><topic>Biological and medical sciences</topic><topic>Chromonar - pharmacology</topic><topic>Coumarins - pharmacology</topic><topic>Dipyridamole - pharmacology</topic><topic>Dogs</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Heart Failure - chemically induced</topic><topic>Heart Failure - prevention & control</topic><topic>Hemodynamics - drug effects</topic><topic>Imipramine - antagonists & inhibitors</topic><topic>Imipramine - poisoning</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Toxicity: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FIEDLER, V. B</creatorcontrib><creatorcontrib>KETTENBACH, B</creatorcontrib><creatorcontrib>GÖBEL, H</creatorcontrib><creatorcontrib>NITZ, R.-E</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><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FIEDLER, V. B</au><au>KETTENBACH, B</au><au>GÖBEL, H</au><au>NITZ, R.-E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of haemodynamic and electrocardiographic side-effects resulting from imipramine toxicity in rats and dogs</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>1985-08</date><risdate>1985</risdate><volume>330</volume><issue>2</issue><spage>155</spage><epage>161</epage><pages>155-161</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><coden>NSAPCC</coden><abstract>This study was designed to analyze the effects of carbocromene and dipyridamole on the haemodynamic and electrocardiographic side-effects resulting from imipramine infusion in anaesthetised rats and dogs. Imipramine was infused at 1 mg/kg/min until cardiac failure and vascular collapse terminated the experiment at 21 +/- 2.3 min in rats and at 29.5 +/- 2.1 min in dogs. This was characterized by hypotension, bradycardia, intraventricular conduction delay, cardiac tachyarrhythmia and A-V block. Carbocromene (4 mg/kg i.v., followed by 80 micrograms/kg/min) protected the animals against heart failure. This was associated with delayed hypotension and negative inotropy, and lower incidence of heart block. Survival time increased to 37 +/- 1.5 min (P less than 0.05), and 54.2 +/- 2.6 min (P less than 0.02) in rats and dogs, respectively. Dipyridamole (0.5 mg/kg i.v., followed by 80 micrograms/kg/min) failed to decrease imipramine toxicity as judged by the haemodynamic and electrocardiographic parameters and did not alter survival time of imipramine controls. These results suggest that carbocromene is an effective treatment for imipramine-induced cardiovascular collapse and cardiac arrhythmias, the beneficial effects being largely due to metabolic and membrane stabilizing effects. Carbocromene has both therapeutic and prophylactic value and appears to be superior to dipyridamole therapy.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><cop>New York, NY</cop><pub>Springer</pub><pmid>4047178</pmid><doi>10.1007/BF00499909</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Arrhythmias, Cardiac - chemically induced Arrhythmias, Cardiac - prevention & control Biological and medical sciences Chromonar - pharmacology Coumarins - pharmacology Dipyridamole - pharmacology Dogs Drug toxicity and drugs side effects treatment Electrocardiography Female Heart Failure - chemically induced Heart Failure - prevention & control Hemodynamics - drug effects Imipramine - antagonists & inhibitors Imipramine - poisoning Male Medical sciences Pharmacology. Drug treatments Rats Toxicity: cardiovascular system |
title | Treatment of haemodynamic and electrocardiographic side-effects resulting from imipramine toxicity in rats and dogs |
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