Antinociceptive and anti-inflammatory effect of Poincianella pyramidalis (Tul.) L.P. Queiroz

Poncianella pyramidalis (Leguminosae) is a Caatinga plant used in folk medicine because of its pharmacological properties, which include anti-inflammatory action. However, chemical compounds responsible for this effect have not yet been identified. This study aimed to evaluate the antioxidant, antin...

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Veröffentlicht in:Journal of ethnopharmacology 2020-05, Vol.254, p.112563, Article 112563
Hauptverfasser: Zelice da Cruz de Moraes, Sabrina, Shan, Andrea Yu Kwan Villar, Oliveira Melo, Marlange Almeida, Pereira da Silva, Juliane, Rocha Santos Passos, Fabiolla, de Souza Graça, Ariel, Araújo, Brancilene Santos de, Quintans, Jullyana de Souza Siqueira, Quintans Júnior, Lucindo José, Oliveira Barreto, Emiliano de, Brandão, Geraldo Célio, Estevam, Charles dos Santos
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Sprache:eng
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Zusammenfassung:Poncianella pyramidalis (Leguminosae) is a Caatinga plant used in folk medicine because of its pharmacological properties, which include anti-inflammatory action. However, chemical compounds responsible for this effect have not yet been identified. This study aimed to evaluate the antioxidant, antinociceptive and anti-inflammatory effects of the ethyl acetate fraction from the inner bark of P. pyramidalis. Total phenol content (TP) was estimated using the Folin-Ciocalteu reagent, while in vitro antioxidant activity was determined by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay. Chemical identification was done using LC-PDA/MS and LC-ESI/MS/MS. In vivo antinociceptive and anti-inflammatory properties were investigated using formalin, mechanical hypernociception and carrageenan-induced pleurisy assays in mice. TP was 525.08 ± 17.49 μg mg−1 gallic acid equivalent. The ethyl acetate fraction (EAF) inhibited 87.76% of the DPPH radical with an EC50 of 22.94 μg mL−1 and Antioxidant Activity Index of 1.74. LC-PDA/MS and LC-ESI/MS/MS identified 15 compounds that are mostly derived from gallic and ellagic acids. Regarding in vivo antinociceptive and anti-inflammatory activity, EAF (100 mg kg-1) significantly reduced the nociceptive response in the second phase of the formalin assay by 50% (p 
ISSN:0378-8741
1872-7573
DOI:10.1016/j.jep.2020.112563