Wallyson André Dos Santos Bezerra, Caio Pavão Tavares, Victor Antônio Silva Lima, Cláudia Quintino da Rocha, Itabajara da Silva Vaz Junior, Paul A M Michels, Livio Martins Costa Junior, Alexandra Martins Dos Santos Soares
{"title":"二聚黄酮类化合物(Brachydins)对小甲鱼谷胱甘肽 S 转移酶的体内和体外评估","authors":"Wallyson André Dos Santos Bezerra, Caio Pavão Tavares, Victor Antônio Silva Lima, Cláudia Quintino da Rocha, Itabajara da Silva Vaz Junior, Paul A M Michels, Livio Martins Costa Junior, Alexandra Martins Dos Santos Soares","doi":"10.2174/0115734064298481240517072216","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong><i>Rhipicephalus microplus</i>, an important cattle ectoparasite, is responsible for a substantial negative impact on the economy due to productivity loss. The emergence of resistance to widely used commercial acaricides has sparked efforts to explore alternative products for tick control.</p><p><strong>Methods: </strong>To address this challenge, innovative solutions targeting essential tick enzymes, like glutathione S-transferase (GST), have gained attention. Dimeric flavonoids, particularly brachydins (BRAs), have demonstrated various biological activities, including antiparasitic effects. The objectives of this study were to isolate four dimeric flavonoids from <i>Fridericia platyphylla</i> roots and to evaluate their potential as inhibitors of <i>R. microplus</i> GST.</p><p><strong>Results: </strong><i>In vitro</i> assays confirmed the inhibition of <i>R. microplus</i> GST by BRA-G, BRA-I, BRA-J, and BRA-K with IC<sub>50</sub> values of 0.075, 0.079, 0.075, and 0.058 mg/mL, respectively, with minimal hemolytic effects. Molecular docking of BRA-G, BRA-I, BRA-J, and BRA-K in a threedimensional model of <i>R. microplus</i> GST revealed predicted interactions with MolDock Scores of - 142.537, -126.831, -108.571, and -123.041, respectively. Both <i>in silico</i> and <i>in vitro</i> analyses show that brachydins are potential inhibitors of <i>R. microplus</i> GST.</p><p><strong>Conclusion: </strong>The findings of this study deepen our understanding of GST inhibition in ticks, affirming its viability as a drug target. This knowledge contributes to the advancement of treatment modalities and strategies for improved tick control.</p>","PeriodicalId":18382,"journal":{"name":"Medicinal Chemistry","volume":" ","pages":"912-919"},"PeriodicalIF":1.9000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>In silico</i> and <i>In vitro</i> Assessment of Dimeric Flavonoids (Brachydins) on <i>Rhipicephalus microplus</i> Glutathione S-transferase.\",\"authors\":\"Wallyson André Dos Santos Bezerra, Caio Pavão Tavares, Victor Antônio Silva Lima, Cláudia Quintino da Rocha, Itabajara da Silva Vaz Junior, Paul A M Michels, Livio Martins Costa Junior, Alexandra Martins Dos Santos Soares\",\"doi\":\"10.2174/0115734064298481240517072216\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong><i>Rhipicephalus microplus</i>, an important cattle ectoparasite, is responsible for a substantial negative impact on the economy due to productivity loss. The emergence of resistance to widely used commercial acaricides has sparked efforts to explore alternative products for tick control.</p><p><strong>Methods: </strong>To address this challenge, innovative solutions targeting essential tick enzymes, like glutathione S-transferase (GST), have gained attention. Dimeric flavonoids, particularly brachydins (BRAs), have demonstrated various biological activities, including antiparasitic effects. The objectives of this study were to isolate four dimeric flavonoids from <i>Fridericia platyphylla</i> roots and to evaluate their potential as inhibitors of <i>R. microplus</i> GST.</p><p><strong>Results: </strong><i>In vitro</i> assays confirmed the inhibition of <i>R. microplus</i> GST by BRA-G, BRA-I, BRA-J, and BRA-K with IC<sub>50</sub> values of 0.075, 0.079, 0.075, and 0.058 mg/mL, respectively, with minimal hemolytic effects. Molecular docking of BRA-G, BRA-I, BRA-J, and BRA-K in a threedimensional model of <i>R. microplus</i> GST revealed predicted interactions with MolDock Scores of - 142.537, -126.831, -108.571, and -123.041, respectively. Both <i>in silico</i> and <i>in vitro</i> analyses show that brachydins are potential inhibitors of <i>R. microplus</i> GST.</p><p><strong>Conclusion: </strong>The findings of this study deepen our understanding of GST inhibition in ticks, affirming its viability as a drug target. 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In silico and In vitro Assessment of Dimeric Flavonoids (Brachydins) on Rhipicephalus microplus Glutathione S-transferase.
Introduction: Rhipicephalus microplus, an important cattle ectoparasite, is responsible for a substantial negative impact on the economy due to productivity loss. The emergence of resistance to widely used commercial acaricides has sparked efforts to explore alternative products for tick control.
Methods: To address this challenge, innovative solutions targeting essential tick enzymes, like glutathione S-transferase (GST), have gained attention. Dimeric flavonoids, particularly brachydins (BRAs), have demonstrated various biological activities, including antiparasitic effects. The objectives of this study were to isolate four dimeric flavonoids from Fridericia platyphylla roots and to evaluate their potential as inhibitors of R. microplus GST.
Results: In vitro assays confirmed the inhibition of R. microplus GST by BRA-G, BRA-I, BRA-J, and BRA-K with IC50 values of 0.075, 0.079, 0.075, and 0.058 mg/mL, respectively, with minimal hemolytic effects. Molecular docking of BRA-G, BRA-I, BRA-J, and BRA-K in a threedimensional model of R. microplus GST revealed predicted interactions with MolDock Scores of - 142.537, -126.831, -108.571, and -123.041, respectively. Both in silico and in vitro analyses show that brachydins are potential inhibitors of R. microplus GST.
Conclusion: The findings of this study deepen our understanding of GST inhibition in ticks, affirming its viability as a drug target. This knowledge contributes to the advancement of treatment modalities and strategies for improved tick control.
期刊介绍:
Aims & Scope
Medicinal Chemistry a peer-reviewed journal, aims to cover all the latest outstanding developments in medicinal chemistry and rational drug design. The journal publishes original research, mini-review articles and guest edited thematic issues covering recent research and developments in the field. Articles are published rapidly by taking full advantage of Internet technology for both the submission and peer review of manuscripts. Medicinal Chemistry is an essential journal for all involved in drug design and discovery.