dc.creator | Muñoz, J. | |
dc.creator | Navarro, C. | |
dc.creator | Noriega, V. | |
dc.creator | Pinardi, | |
dc.creator | Sierralta, F. | |
dc.creator | Prieto, J. C. | |
dc.creator | Miranda, H. F. | |
dc.date.accessioned | 2019-03-11T12:59:21Z | |
dc.date.available | 2019-03-11T12:59:21Z | |
dc.date.created | 2019-03-11T12:59:21Z | |
dc.date.issued | 2010 | |
dc.identifier | Inflammopharmacology, Volumen 18, Issue 2, 2018, Pages 65-71 | |
dc.identifier | 09254692 | |
dc.identifier | 10.1007/s10787-009-0019-7 | |
dc.identifier | https://repositorio.uchile.cl/handle/2250/164987 | |
dc.description.abstract | Objective and design: The antinociception induced by the intraperitoneal coadministration in mice of combinations of metamizol and paracetamol was evaluated in the tail flick test and orofacial formalin test. Methods: The antinociception of each drugs alone and the interaction of the combinations was evaluated by isobolographic analysis in the tail-flick and in the formalin orofacial assay of mice. Results: Mice pretreated with the drugs demonstrated that the antinociception of metamizol and paracetamol is dose-dependent. The potency range on the antinocifensive responses for metamizol or paracetamol was as follows: orofacial (Phase II) > orofacial (Phase I) > tail flick. In addition, the coadministration of metamizol with paracetamol induced a strong synergistic antinociception in the algesiometer assays. Both drugs showed effectiveness in inflammatory pain. Conclusion: These actions can be related to the differential selectivity of the drugs for inhibition of COX isoforms and also to | |
dc.language | en | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
dc.source | Inflammopharmacology | |
dc.subject | Analgesia | |
dc.subject | Metamizol | |
dc.subject | Pain | |
dc.subject | Paracetamol | |
dc.subject | Synergism | |
dc.title | Synergism between COX-3 inhibitors in two animal models of pain | |
dc.type | Artículo de revista | |