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
Hauptverfasser: FIEDLER, V. B, KETTENBACH, B, GÖBEL, H, NITZ, R.-E
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creator FIEDLER, V. B
KETTENBACH, B
GÖBEL, H
NITZ, R.-E
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.
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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. 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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 &amp; 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 &amp; control</subject><subject>Hemodynamics - drug effects</subject><subject>Imipramine - antagonists &amp; inhibitors</subject><subject>Imipramine - poisoning</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pharmacology. 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identifier ISSN: 0028-1298
ispartof Naunyn-Schmiedeberg's archives of pharmacology, 1985-08, Vol.330 (2), p.155-161
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1432-1912
language eng
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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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