L. S. Frota, Francisco Glerison da Silva Nascimento, Leonardo Soares Freitas, Francisco F. S. Lopes, Ramon Róseo Paula Pessoa Bezerra de Menezes, A. F. Pires, R. Castro, A. Assreuy, S. M. D. Morais
{"title":"The Amentoflavone-Rich Extract of Ouratea fieldingiana Leaves Presents Antioxidant and Anti-inflammatory Activity in Mice","authors":"L. S. Frota, Francisco Glerison da Silva Nascimento, Leonardo Soares Freitas, Francisco F. S. Lopes, Ramon Róseo Paula Pessoa Bezerra de Menezes, A. F. Pires, R. Castro, A. Assreuy, S. M. D. Morais","doi":"10.9734/acri/2024/v24i4660","DOIUrl":null,"url":null,"abstract":"Aims: To evaluate the antioxidant and anti-inflammatory effects of the Ouratea fieldingiana leaf extract (OFE) and its main constituent amentoflavone (AMT).\nStudy Design: The phenolic compounds of Ouratea fieldingiana leaves (OFE) were quantified, the chemical structure characterized and the anti-inflammatory effect of OFE and amentoflavone was evaluated in mice paw edema and peritonitis.\nPlace and Duration of Study: The work involved the partnership of the Natural Products Chemistry Laboratory and Inflammation Physio pharmacology Laboratory, between July 2020 and June 2021.\nMethodology: The OFE was obtained from 70% ethanol extract of O. fieldingiana. OFE was subjected to classic chromatographic column furnishing AMT. The phenolic compounds were characterized by HPLC and quantified by Follin-Ciocalteu methodology. The antiradical potential was evaluated by DPPH and ABTS methods. Anti-inflammatory activity was determined in female Swiss mice received per oral OFE (0.1-10 mg/kg) or sterile saline 60 min before stimulation with carrageenan (300 mg) for quantification of the parameters: edema, abdominal hypernociception, neutrophil migration and oxidative stress markers (reduced glutathione, malondialdehyde, myeloperoxidase and catalase activities).\nResults: AMT was identified as the main compound in the OFE (292.64 ± 3.87 mg/g extract). OFE has an average inhibitory concentration of 9.81 ± 0.17 µg/mL extract to inhibit the DPPH radical. OFE and AMT inhibited paw edema [OFE: 32% (0-2 h), 28% (2-4 h); AMT: 55% (0-2h); 51% (2-4 h)], neutrophil migration (OFE: 65%; AMT: 67%); myeloperoxidase activity (OFE: 37%; AMT: 45%) and abdominal hypernociception (OFE: 31%; AMT: 35%). OFE, but not AMT, increased catalase activity (57%) and reduced glutathione (62%), but decreased malondialdehyde (69%).\nConclusion: The amentoflavone-rich extract from O. fieldingiana leaves presents antioxidant activity in vitro and in vivo, and anti-inflammatory activity in vivo, corroborating the popular use of the plant.","PeriodicalId":505151,"journal":{"name":"Archives of Current Research International","volume":"82 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Current Research International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/acri/2024/v24i4660","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aims: To evaluate the antioxidant and anti-inflammatory effects of the Ouratea fieldingiana leaf extract (OFE) and its main constituent amentoflavone (AMT).
Study Design: The phenolic compounds of Ouratea fieldingiana leaves (OFE) were quantified, the chemical structure characterized and the anti-inflammatory effect of OFE and amentoflavone was evaluated in mice paw edema and peritonitis.
Place and Duration of Study: The work involved the partnership of the Natural Products Chemistry Laboratory and Inflammation Physio pharmacology Laboratory, between July 2020 and June 2021.
Methodology: The OFE was obtained from 70% ethanol extract of O. fieldingiana. OFE was subjected to classic chromatographic column furnishing AMT. The phenolic compounds were characterized by HPLC and quantified by Follin-Ciocalteu methodology. The antiradical potential was evaluated by DPPH and ABTS methods. Anti-inflammatory activity was determined in female Swiss mice received per oral OFE (0.1-10 mg/kg) or sterile saline 60 min before stimulation with carrageenan (300 mg) for quantification of the parameters: edema, abdominal hypernociception, neutrophil migration and oxidative stress markers (reduced glutathione, malondialdehyde, myeloperoxidase and catalase activities).
Results: AMT was identified as the main compound in the OFE (292.64 ± 3.87 mg/g extract). OFE has an average inhibitory concentration of 9.81 ± 0.17 µg/mL extract to inhibit the DPPH radical. OFE and AMT inhibited paw edema [OFE: 32% (0-2 h), 28% (2-4 h); AMT: 55% (0-2h); 51% (2-4 h)], neutrophil migration (OFE: 65%; AMT: 67%); myeloperoxidase activity (OFE: 37%; AMT: 45%) and abdominal hypernociception (OFE: 31%; AMT: 35%). OFE, but not AMT, increased catalase activity (57%) and reduced glutathione (62%), but decreased malondialdehyde (69%).
Conclusion: The amentoflavone-rich extract from O. fieldingiana leaves presents antioxidant activity in vitro and in vivo, and anti-inflammatory activity in vivo, corroborating the popular use of the plant.