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Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac

Although nonsteroidal anti-inflammatory drugs (NSAIDs) are one of the main types of drugs used to treat pain, they have several adverse effects, and such effects can be reduced by combining two analgesic drugs. The aim of this study was to evaluate the nociceptive activity of methyleugenol combined...

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Autores principales: Rocha-González, Héctor Isaac, Sánchez-Mendoza, María Elena, Cruz-Antonio, Leticia, Flores-Murrieta, Francisco Javier, Cornelio-Huerta, Xochilt Itzel, Arrieta, Jesús
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663170/
https://www.ncbi.nlm.nih.gov/pubmed/33153182
http://dx.doi.org/10.3390/molecules25215106
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author Rocha-González, Héctor Isaac
Sánchez-Mendoza, María Elena
Cruz-Antonio, Leticia
Flores-Murrieta, Francisco Javier
Cornelio-Huerta, Xochilt Itzel
Arrieta, Jesús
author_facet Rocha-González, Héctor Isaac
Sánchez-Mendoza, María Elena
Cruz-Antonio, Leticia
Flores-Murrieta, Francisco Javier
Cornelio-Huerta, Xochilt Itzel
Arrieta, Jesús
author_sort Rocha-González, Héctor Isaac
collection PubMed
description Although nonsteroidal anti-inflammatory drugs (NSAIDs) are one of the main types of drugs used to treat pain, they have several adverse effects, and such effects can be reduced by combining two analgesic drugs. The aim of this study was to evaluate the nociceptive activity of methyleugenol combined with either diclofenac or ketorolac, and determine certain parameters of pharmacokinetics. For the isobolographic analysis, the experimental effective dose 30 (ED(30)) was calculated for the drugs applied individually. With these effective doses, the peak plasma concentration (C(max)) was found and the other parameters of pharmacokinetics were established. Methyleugenol plus diclofenac and methyleugenol plus ketorolac decreased licking behavior in a dose-dependent manner in phase II, with an efficacy of 32.9 ± 9.3 and 39.8 ± 9.6%, respectively. According to the isobolographic analysis, the experimental and theoretical ED(30) values were similar for methyleugenol plus diclofenac, suggesting an additive effect, but significantly different for methyleugenol plus ketorolac (3.6 ± 0.5 vs. 7.7 ± 0.6 mg/kg, respectively), indicating a probable synergistic interaction. Regarding pharmacokinetics, the only parameter showing a significant difference was C(max) for the methyleugenol plus diclofenac combination. Even with this difference, the combinations studied may be advantageous for treating inflammatory pain, especially for the combination methyleugenol plus ketorolac.
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spelling pubmed-76631702020-11-14 Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac Rocha-González, Héctor Isaac Sánchez-Mendoza, María Elena Cruz-Antonio, Leticia Flores-Murrieta, Francisco Javier Cornelio-Huerta, Xochilt Itzel Arrieta, Jesús Molecules Article Although nonsteroidal anti-inflammatory drugs (NSAIDs) are one of the main types of drugs used to treat pain, they have several adverse effects, and such effects can be reduced by combining two analgesic drugs. The aim of this study was to evaluate the nociceptive activity of methyleugenol combined with either diclofenac or ketorolac, and determine certain parameters of pharmacokinetics. For the isobolographic analysis, the experimental effective dose 30 (ED(30)) was calculated for the drugs applied individually. With these effective doses, the peak plasma concentration (C(max)) was found and the other parameters of pharmacokinetics were established. Methyleugenol plus diclofenac and methyleugenol plus ketorolac decreased licking behavior in a dose-dependent manner in phase II, with an efficacy of 32.9 ± 9.3 and 39.8 ± 9.6%, respectively. According to the isobolographic analysis, the experimental and theoretical ED(30) values were similar for methyleugenol plus diclofenac, suggesting an additive effect, but significantly different for methyleugenol plus ketorolac (3.6 ± 0.5 vs. 7.7 ± 0.6 mg/kg, respectively), indicating a probable synergistic interaction. Regarding pharmacokinetics, the only parameter showing a significant difference was C(max) for the methyleugenol plus diclofenac combination. Even with this difference, the combinations studied may be advantageous for treating inflammatory pain, especially for the combination methyleugenol plus ketorolac. MDPI 2020-11-03 /pmc/articles/PMC7663170/ /pubmed/33153182 http://dx.doi.org/10.3390/molecules25215106 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rocha-González, Héctor Isaac
Sánchez-Mendoza, María Elena
Cruz-Antonio, Leticia
Flores-Murrieta, Francisco Javier
Cornelio-Huerta, Xochilt Itzel
Arrieta, Jesús
Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac
title Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac
title_full Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac
title_fullStr Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac
title_full_unstemmed Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac
title_short Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac
title_sort antinociceptive interaction and pharmacokinetics of the combination treatments of methyleugenol plus diclofenac or ketorolac
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663170/
https://www.ncbi.nlm.nih.gov/pubmed/33153182
http://dx.doi.org/10.3390/molecules25215106
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