The antinociceptive and anti-inflammatory activities of Piptadenia stipulacea Benth. (Fabaceae) |
| |
Authors: | Aline Cavalcanti de Queiroz,Daysianne Pereira de Lira,Thays de Lima Matos Freire Dias,É verton Tenó rio de Souza,Carolina Barbosa Brito da Matta,Anansa Bezerra de Aquino,Luiz Henrique Agra Cavalcante Silva,Diogo José Costa da Silva,Eliane Aparecida Campessato Mella,Maria de Fá tima Agra,José Maria Barbosa Filho,Joã o Xavier de Araú jo-Jú nior,Bá rbara Viviana de Oliveira Santos,Magna Suzana Alexandre-Moreira |
| |
Affiliation: | 1. LaFI - Laboratório de Farmacologia e Imunidade, Instituto de Ciências Biológicas e da Saúde, Universidade Federal de Alagoas, Maceió, AL, Brazil;2. Laboratório de Tecnologia Farmacêutica, Universidade Federal da Paraíba, PB, Brazil;3. Laboratório de Pesquisa em Recursos Naturais, Instituto de Química e Biotecnologia, Universidade Federal de Alagoas, Maceió, AL, Brazil;4. Escola de Enfermagem e Farmácia, Universidade Federal de Alagoas, Maceió, AL, Brazil |
| |
Abstract: | AimIn this study, we attempted to identify the possible antinociceptive and anti-inflammatory actions of the aqueous phase, the ethyl acetate phase and one unknown flavonoid obtained from aerial parts of Piptadenia stipulacea, known in Brazil as “jurema-branca”, “carcará” and “rasga-beiço”.Materials and methodsAerial parts of Piptadenia stipulacea were used and after fractionation, the flavonoid FGAL was obtained. Experiments were conducted on Swiss mice using the acetic acid-induced writhing test, the hot plate test, the formalin-induced pain test and zymosan A-induced peritonitis test.ResultsThe aqueous and ethyl acetate phases (p.o., 100 mg/kg); and the flavonoid FGAL (p.o. and i.p. at 100 μmol/kg), reduced the nociception produced by acetic acid, by 49.92%, 54.62%, 38.97% and 64.79%, respectively. In vivo inhibition of nociception by the ethyl acetate phase (100 mg/kg, p.o.) in the hot plate test was favorable, indicating that this fraction exhibited central activity. The ethyl acetate phase (100 mg/kg, p.o.) reduced the formalin effects in both phases by 28.51% and 55.72%, respectively. Treatment with the aqueous phase (100 mg/kg, p.o.) and FGAL (100 μmol/kg, i.p.) only protected the second phase by 69.76% and 68.78%, respectively. In addition, it was observed in the zymosan A-induced peritonitis test that the aqueous phase, the ethyl acetate phase and the FGAL exhibited anti-inflammatory activity, reducing significantly the number of recruit cells by 35.84%, 37.70% and FGAL (1), respectively.ConclusionsThese data demonstrate that the FGAL elicits pronounced antinociceptive activity against several pain models. The actions of this flavonoid probably are due to antioxidative properties. However, pharmacological and chemical studies are continuing in order to characterize the mechanism(s) responsible for this antinociceptive action and also to identify other active substances present in Piptadenia stipulacea. |
| |
Keywords: | Antinociceptive Anti-inflammatory Piptadenia stipulacea Flavonoids |
本文献已被 ScienceDirect 等数据库收录! |
|