麻麻醇提物抗氧化、抗焦虑活性的UPLC-PDA-ESI-QDA表征与评价Hauenschild叶子

Natália Kelly Gomes de Carvalho , Mariana Pereira da Silva , Débora Odília Duarte Leite , Gerson Javier Torres Salazar , Johnatan Wellisson da Silva Mendes , Kirley Marques Canuto , Paulo Riceli Vasconcelos Ribeiro , Amanda Maria Barros Alves , Ivana Carneiro Romão , Hélcio Silva dos Santos , José Galberto Martins da Costa
{"title":"麻麻醇提物抗氧化、抗焦虑活性的UPLC-PDA-ESI-QDA表征与评价Hauenschild叶子","authors":"Natália Kelly Gomes de Carvalho ,&nbsp;Mariana Pereira da Silva ,&nbsp;Débora Odília Duarte Leite ,&nbsp;Gerson Javier Torres Salazar ,&nbsp;Johnatan Wellisson da Silva Mendes ,&nbsp;Kirley Marques Canuto ,&nbsp;Paulo Riceli Vasconcelos Ribeiro ,&nbsp;Amanda Maria Barros Alves ,&nbsp;Ivana Carneiro Romão ,&nbsp;Hélcio Silva dos Santos ,&nbsp;José Galberto Martins da Costa","doi":"10.1016/j.prenap.2025.100223","DOIUrl":null,"url":null,"abstract":"<div><div>Sarcomphalus joazeiro (Rhamnaceae) demonstrated antioxidant activity and effects on the central nervous system (CNS), being considered an alternative for preclinical investigations of anxiolytic drugs. The aim of this study was to evaluate the chemical composition, antioxidant capacity and anxiolytic effect of the ethanolic extract of the leaves of S. joazeiro (EEFSJ). The chemical profile was analyzed by liquid chromatography coupled to mass spectrometry (UPLC-PDA-ESI-QDA). The antioxidant activity was evaluated using DPPH• and ABTS•⁺ capture assays. Acute toxicity tests for 96 h, open field and light/dark tests were applied in vivo to evaluate the sedative and anxiolytic effects, respectively, using zebrafish of both sexes with n = 6/treatment group, at doses of 40, 200 and 400 mg/kg. A total of 5 groups were formed. For the mechanism of action test, the antagonist flumazenil (FMZ) group was also included in the sample. Eleven compounds from the flavonoid and saponin classes were identified. EEFSJ showed a median inhibitory concentration (IC50) of 185.2 ± 2.2 µg/mL and 74.17 ± 1.5 µg/mL against DPPH• and ABTS•⁺ radicals, respectively. At low doses, EEFSJ may have an anxiolytic effect; however, as the doses increase, the sedative effect becomes predominant and no toxicity was observed after 96 h, and its mechanism of action is related to GABAergic modulation. Thus, it is necessary to evaluate the pharmacological profile of EEFSJ in chronic models of anxiety and oxidative stress, as well as to extend the studies to mammals, exploring potential clinical applications and long-term safety.</div></div>","PeriodicalId":101014,"journal":{"name":"Pharmacological Research - Natural Products","volume":"7 ","pages":"Article 100223"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"UPLC-PDA-ESI-QDA characterization and evaluation of the antioxidant and anxiolytic activities of the ethanolic extract of Sarcomphalus joazeiro (Mart.) Hauenschild leaves\",\"authors\":\"Natália Kelly Gomes de Carvalho ,&nbsp;Mariana Pereira da Silva ,&nbsp;Débora Odília Duarte Leite ,&nbsp;Gerson Javier Torres Salazar ,&nbsp;Johnatan Wellisson da Silva Mendes ,&nbsp;Kirley Marques Canuto ,&nbsp;Paulo Riceli Vasconcelos Ribeiro ,&nbsp;Amanda Maria Barros Alves ,&nbsp;Ivana Carneiro Romão ,&nbsp;Hélcio Silva dos Santos ,&nbsp;José Galberto Martins da Costa\",\"doi\":\"10.1016/j.prenap.2025.100223\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Sarcomphalus joazeiro (Rhamnaceae) demonstrated antioxidant activity and effects on the central nervous system (CNS), being considered an alternative for preclinical investigations of anxiolytic drugs. The aim of this study was to evaluate the chemical composition, antioxidant capacity and anxiolytic effect of the ethanolic extract of the leaves of S. joazeiro (EEFSJ). The chemical profile was analyzed by liquid chromatography coupled to mass spectrometry (UPLC-PDA-ESI-QDA). The antioxidant activity was evaluated using DPPH• and ABTS•⁺ capture assays. Acute toxicity tests for 96 h, open field and light/dark tests were applied in vivo to evaluate the sedative and anxiolytic effects, respectively, using zebrafish of both sexes with n = 6/treatment group, at doses of 40, 200 and 400 mg/kg. A total of 5 groups were formed. For the mechanism of action test, the antagonist flumazenil (FMZ) group was also included in the sample. Eleven compounds from the flavonoid and saponin classes were identified. EEFSJ showed a median inhibitory concentration (IC50) of 185.2 ± 2.2 µg/mL and 74.17 ± 1.5 µg/mL against DPPH• and ABTS•⁺ radicals, respectively. At low doses, EEFSJ may have an anxiolytic effect; however, as the doses increase, the sedative effect becomes predominant and no toxicity was observed after 96 h, and its mechanism of action is related to GABAergic modulation. Thus, it is necessary to evaluate the pharmacological profile of EEFSJ in chronic models of anxiety and oxidative stress, as well as to extend the studies to mammals, exploring potential clinical applications and long-term safety.</div></div>\",\"PeriodicalId\":101014,\"journal\":{\"name\":\"Pharmacological Research - Natural Products\",\"volume\":\"7 \",\"pages\":\"Article 100223\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacological Research - Natural Products\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2950199725000837\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacological Research - Natural Products","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950199725000837","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

鼠李科(Rhamnaceae)具有抗氧化活性和对中枢神经系统(CNS)的影响,被认为是抗焦虑药物临床前研究的替代方案。摘要本研究旨在研究荆芥叶乙醇提取物(EEFSJ)的化学成分、抗氧化能力和抗焦虑作用。采用液相色谱-质谱联用(UPLC-PDA-ESI-QDA)分析。采用DPPH•和ABTS•捕获法评估其抗氧化活性。采用96 h急性毒性试验、野外试验和光/暗试验,分别在体内评价其镇静和抗焦虑作用,试验对象为雌雄斑马鱼,n = 6/治疗组,剂量分别为40、200和400 mg/kg。共组成5组。为了进行作用机制试验,还将拮抗剂氟马西尼(FMZ)组纳入样本。从黄酮类和皂苷类中鉴定出11个化合物。EEFSJ对DPPH•和ABTS•+自由基的中位抑制浓度(IC50)分别为185.2 ± 2.2 µg/mL和74.17 ± 1.5 µg/mL。低剂量时,EEFSJ可能具有抗焦虑作用;但随着剂量的增加,镇静作用逐渐明显,96 h后无毒性反应,其作用机制与gaba能调节有关。因此,有必要评估EEFSJ在慢性焦虑和氧化应激模型中的药理学特征,并将研究扩展到哺乳动物,探索其潜在的临床应用和长期安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
UPLC-PDA-ESI-QDA characterization and evaluation of the antioxidant and anxiolytic activities of the ethanolic extract of Sarcomphalus joazeiro (Mart.) Hauenschild leaves
Sarcomphalus joazeiro (Rhamnaceae) demonstrated antioxidant activity and effects on the central nervous system (CNS), being considered an alternative for preclinical investigations of anxiolytic drugs. The aim of this study was to evaluate the chemical composition, antioxidant capacity and anxiolytic effect of the ethanolic extract of the leaves of S. joazeiro (EEFSJ). The chemical profile was analyzed by liquid chromatography coupled to mass spectrometry (UPLC-PDA-ESI-QDA). The antioxidant activity was evaluated using DPPH• and ABTS•⁺ capture assays. Acute toxicity tests for 96 h, open field and light/dark tests were applied in vivo to evaluate the sedative and anxiolytic effects, respectively, using zebrafish of both sexes with n = 6/treatment group, at doses of 40, 200 and 400 mg/kg. A total of 5 groups were formed. For the mechanism of action test, the antagonist flumazenil (FMZ) group was also included in the sample. Eleven compounds from the flavonoid and saponin classes were identified. EEFSJ showed a median inhibitory concentration (IC50) of 185.2 ± 2.2 µg/mL and 74.17 ± 1.5 µg/mL against DPPH• and ABTS•⁺ radicals, respectively. At low doses, EEFSJ may have an anxiolytic effect; however, as the doses increase, the sedative effect becomes predominant and no toxicity was observed after 96 h, and its mechanism of action is related to GABAergic modulation. Thus, it is necessary to evaluate the pharmacological profile of EEFSJ in chronic models of anxiety and oxidative stress, as well as to extend the studies to mammals, exploring potential clinical applications and long-term safety.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信