Please use this identifier to cite or link to this item: http://www.repositorio.ufc.br/handle/riufc/8507
Title in Portuguese: Synergistic effect of the L-tryptophan and kynurenic acid with dipyrone or paracetamol in mice
Author: Rocha, Nayrton Flávio Moura
Rios, Emiliano Ricardo Vasconcelos
Carvalho, Alyne Mara Rodrigues
Freire, Leonardo Vasconcelos
Dias, Marília Leite
Fonteles, Marta Maria de França
Sousa, Francisca Cléa Florenço de
Keywords: Dipirona
Acetaminofen
Issue Date: 2013
Publisher: Chemico-Biological Interactions
Citation: ROCHA, N. F. M. et al. Synergistic effect of the L-tryptophan and kynurenic acid with dipyrone or paracetamol in mice. Chemico-Biological Interactions, v. 205, n. 2, p. 148-156, 2013.
Abstract: Purpose: Our great interest in this work was study the synergism between L-tryptophan and dipyrone or paracetamol as well as the interaction of kynurenic acid (L-tryptophan metabolite) and these analgesics agents utilizing a robust methodology. Methods: We performed the writhing test induced by acetic acid in mice to evaluate the antinociceptive effect of the treatments isolated and combined (p.o. and i.p.). Dose–response curves were constructed and the values of ED50 for treatment alone and combined were statistically compared. In addition, isobolographic analysis was performed and the experimental values were compared with the theoretical values for simple additive effect. Results: The combined treatment with L-tryptophan and dipyrone or paracetamol reduced significantly the ED50 of these analgesics when compared to the isolated treatments. L-tryptophan alone has no antinociceptive effect. L-Tryptophan increases the central amount of 5-HT and the synergism with dipyrone is antagonized by the 5-HT depletion. The kyna has an antinociceptive dose-related effect and a synergistic interaction with dipyrone and paracetamol verified by isobolographic analyses and confirmed by experimental values of ED50 of combined treatments were statistically lower than theoretical calculated values for simple additive effect. Melatonin antagonist receptor attenuates the antinociceptive synergism between L-tryptophan and dipyrone. Conclusion: Our results demonstrate that the increased 5-HT amount on the central nervous system is not per se capable to induce antinociception. The L-tryptophan interacts synergistically with dipyrone and paracetamol both orally and by i.p. route. This effect is dependent on the biotransformation of L-tryptophan to 5-HT and involves kynurenic acid and melatonin receptors.
URI: http://www.repositorio.ufc.br/handle/riufc/8507
metadata.dc.type: Artigo
ISSN: 0009-2797
Appears in Collections:DFAR - Artigos publicados em revistas científicas

Files in This Item:
File Description SizeFormat 
2013_art_rervrios.pdf991,11 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.