Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice

Introduction: Tricyclic antidepressant have been shown to be effective in treatment of pain of varying etiology, monoaminergic system seems to be implicated in this phenomena. This research examines the role of beta-adrenergic receptor blockers on the antinociceptive effect of imipramine in albino m...

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Main Authors: H A Zawia, F A Blaou, A S Elhwuegi
Format: Article
Language:English
Published: Thieme Medical and Scientific Publishers Pvt. Ltd. 2016-01-01
Series:Libyan International Medical University Journal
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Online Access:http://www.thieme-connect.de/DOI/DOI?10.21502/limuj.003.01.2016
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author H A Zawia
F A Blaou
A S Elhwuegi
author_facet H A Zawia
F A Blaou
A S Elhwuegi
author_sort H A Zawia
collection DOAJ
description Introduction: Tricyclic antidepressant have been shown to be effective in treatment of pain of varying etiology, monoaminergic system seems to be implicated in this phenomena. This research examines the role of beta-adrenergic receptor blockers on the antinociceptive effect of imipramine in albino mice using thermal model of pain. Methods: Different groups of five animals each were injected intraperitoneal by different doses of imipramine only (2.5, 7.5,15, 30 mg/kg), atenolol (2 mg/kg), propranolol (6mg/kg), or the combination of the different doses of imipramine with the fixed dose of atenolol or propranolol. The degree of analgesia was measured as an increase in reaction time to pain in the hot plate one hour after drugs injections. Results: Imipramine produced dose dependent increase in reaction time from 129% with the lowest dose to 196% with the highest dose. One-way ANOVA analysis has shown that the addition of a fixed dose of propranolol antagonized significantly the increase in reaction time to 75% with the lowest dose and 118.9% with the highest dose of imipramine. On the other hand, atenolol failed to antagonize significantly the increase in reaction time induced by imipramine. Conclusion: Imipramine has a significant analgesic effect on albino mice in the hot plate test. The antinociceptive action of imipramine seems to be of central origin and possibly mediated, at least in part, by beta adrenergic receptors, as this analgesic effect can be blocked by propranolol, a centrally acting non-selective beta adrenergic receptor antagonist, but not with atenolol which blocks only the peripheral beta receptors.
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spelling doaj-art-dce20d78f3474d599f772eacbb29ce002025-08-20T02:54:46ZengThieme Medical and Scientific Publishers Pvt. Ltd.Libyan International Medical University Journal2519-139X2016-01-010101172610.21502/limuj.003.01.20163Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino miceH A Zawia0F A Blaou1A S Elhwuegi2Department of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, University of Tripoli, Tripoli, LibyaDepartment of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, University of Tripoli, Tripoli, LibyaDepartment of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, University of Tripoli, Tripoli, LibyaIntroduction: Tricyclic antidepressant have been shown to be effective in treatment of pain of varying etiology, monoaminergic system seems to be implicated in this phenomena. This research examines the role of beta-adrenergic receptor blockers on the antinociceptive effect of imipramine in albino mice using thermal model of pain. Methods: Different groups of five animals each were injected intraperitoneal by different doses of imipramine only (2.5, 7.5,15, 30 mg/kg), atenolol (2 mg/kg), propranolol (6mg/kg), or the combination of the different doses of imipramine with the fixed dose of atenolol or propranolol. The degree of analgesia was measured as an increase in reaction time to pain in the hot plate one hour after drugs injections. Results: Imipramine produced dose dependent increase in reaction time from 129% with the lowest dose to 196% with the highest dose. One-way ANOVA analysis has shown that the addition of a fixed dose of propranolol antagonized significantly the increase in reaction time to 75% with the lowest dose and 118.9% with the highest dose of imipramine. On the other hand, atenolol failed to antagonize significantly the increase in reaction time induced by imipramine. Conclusion: Imipramine has a significant analgesic effect on albino mice in the hot plate test. The antinociceptive action of imipramine seems to be of central origin and possibly mediated, at least in part, by beta adrenergic receptors, as this analgesic effect can be blocked by propranolol, a centrally acting non-selective beta adrenergic receptor antagonist, but not with atenolol which blocks only the peripheral beta receptors.http://www.thieme-connect.de/DOI/DOI?10.21502/limuj.003.01.2016imipramineatenololpropranololanalgesiathermal nociception
spellingShingle H A Zawia
F A Blaou
A S Elhwuegi
Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
Libyan International Medical University Journal
imipramine
atenolol
propranolol
analgesia
thermal nociception
title Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
title_full Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
title_fullStr Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
title_full_unstemmed Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
title_short Beta-adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
title_sort beta adrenergic receptor blockers effects on the antinociceptive action of imipramine against thermal induced pain in albino mice
topic imipramine
atenolol
propranolol
analgesia
thermal nociception
url http://www.thieme-connect.de/DOI/DOI?10.21502/limuj.003.01.2016
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AT aselhwuegi betaadrenergicreceptorblockerseffectsontheantinociceptiveactionofimipramineagainstthermalinducedpaininalbinomice