Back to Search Start Over

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

Authors :
Rocha-González HI
Sánchez-Mendoza ME
Cruz-Antonio L
Flores-Murrieta FJ
Cornelio-Huerta XI
Arrieta J
Source :
Molecules (Basel, Switzerland) [Molecules] 2020 Nov 03; Vol. 25 (21). Date of Electronic Publication: 2020 Nov 03.
Publication Year :
2020

Abstract

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 <subscript>30</subscript> ) was calculated for the drugs applied individually. With these effective doses, the peak plasma concentration (C <subscript>max</subscript> ) 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 <subscript>30</subscript> 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 <subscript>max</subscript> 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.

Details

Language :
English
ISSN :
1420-3049
Volume :
25
Issue :
21
Database :
MEDLINE
Journal :
Molecules (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
33153182
Full Text :
https://doi.org/10.3390/molecules25215106