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The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice
BACKGROUND: Combination analgesics provide more effective pain relief for a broader spectrum of pain. This research examines the possible potentiation of the analgesic effect of different classes of antidepressants when combined with aspirin in thermal model of pain using Albino mice. METHODS: Diffe...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332043/ https://www.ncbi.nlm.nih.gov/pubmed/22529878 http://dx.doi.org/10.3402/ljm.v7i0.17251 |
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author | Elhwuegi, Abdalla S. Hassan, Kalthom M. |
author_facet | Elhwuegi, Abdalla S. Hassan, Kalthom M. |
author_sort | Elhwuegi, Abdalla S. |
collection | PubMed |
description | BACKGROUND: Combination analgesics provide more effective pain relief for a broader spectrum of pain. This research examines the possible potentiation of the analgesic effect of different classes of antidepressants when combined with aspirin in thermal model of pain using Albino mice. METHODS: Different groups of six animals each were injected intraperitoneally by different doses of aspirin (50, 100, or 200 mg/kg), imipramine (2.5, 7.5, 15 or 30 mg/kg), fluoxetine (1.25, 2.5, 5 or 7.5 mg/kg), mirtazapine (1.25, 2.5, or 5 mg/kg) and a combination of a fixed dose of aspirin (100 mg/kg) with the different doses of the three antidepressants. One hour later the analgesic effect of these treatments were evaluated against thermally induced pain. All data were subjected to statistical analysis using unpaired Student's t-test. RESULTS: Aspirin had no analgesic effect in thermally induced pain. The three selected antidepressants produced dose dependent analgesia. The addition of a fixed dose of aspirin to imipramine significantly increased the reaction time (RT) of the lowest dose (by 23%) and the highest dose (by 20%). The addition of the fixed dose of aspirin to fluoxetine significantly increased RT by 13% of the dose 2.5 mg/kg. Finally, the addition of the fixed dose of aspirin significantly potentiated the antinociceptive effect of the different doses of mirtazapine (RT was increased by 24, 54 and 38% respectively). CONCLUSION: Combination of aspirin with an antidepressant might produce better analgesia, increasing the efficacy of pain management and reduces side effects by using smaller doses of each drug. |
format | Online Article Text |
id | pubmed-3332043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-33320432012-04-23 The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice Elhwuegi, Abdalla S. Hassan, Kalthom M. Libyan J Med Research Article BACKGROUND: Combination analgesics provide more effective pain relief for a broader spectrum of pain. This research examines the possible potentiation of the analgesic effect of different classes of antidepressants when combined with aspirin in thermal model of pain using Albino mice. METHODS: Different groups of six animals each were injected intraperitoneally by different doses of aspirin (50, 100, or 200 mg/kg), imipramine (2.5, 7.5, 15 or 30 mg/kg), fluoxetine (1.25, 2.5, 5 or 7.5 mg/kg), mirtazapine (1.25, 2.5, or 5 mg/kg) and a combination of a fixed dose of aspirin (100 mg/kg) with the different doses of the three antidepressants. One hour later the analgesic effect of these treatments were evaluated against thermally induced pain. All data were subjected to statistical analysis using unpaired Student's t-test. RESULTS: Aspirin had no analgesic effect in thermally induced pain. The three selected antidepressants produced dose dependent analgesia. The addition of a fixed dose of aspirin to imipramine significantly increased the reaction time (RT) of the lowest dose (by 23%) and the highest dose (by 20%). The addition of the fixed dose of aspirin to fluoxetine significantly increased RT by 13% of the dose 2.5 mg/kg. Finally, the addition of the fixed dose of aspirin significantly potentiated the antinociceptive effect of the different doses of mirtazapine (RT was increased by 24, 54 and 38% respectively). CONCLUSION: Combination of aspirin with an antidepressant might produce better analgesia, increasing the efficacy of pain management and reduces side effects by using smaller doses of each drug. Co-Action Publishing 2012-04-19 /pmc/articles/PMC3332043/ /pubmed/22529878 http://dx.doi.org/10.3402/ljm.v7i0.17251 Text en © 2012 Abdalla S. Elhwuegi and Kalthom M. Hassan http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Elhwuegi, Abdalla S. Hassan, Kalthom M. The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice |
title | The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice |
title_full | The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice |
title_fullStr | The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice |
title_full_unstemmed | The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice |
title_short | The analgesic effect of different antidepressants combined with aspirin on thermally induced pain in Albino mice |
title_sort | analgesic effect of different antidepressants combined with aspirin on thermally induced pain in albino mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332043/ https://www.ncbi.nlm.nih.gov/pubmed/22529878 http://dx.doi.org/10.3402/ljm.v7i0.17251 |
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