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

IF 1.9 4区 医学 Q3 CHEMISTRY, MEDICINAL
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
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引用次数: 0

摘要

导言:Rhipicephalus microplus 是一种重要的牛体外寄生虫,由于生产力损失,它对经济造成了巨大的负面影响。广泛使用的商业杀螨剂出现了抗药性,这促使人们努力探索控制蜱虫的替代产品:方法:为应对这一挑战,针对蜱的基本酶(如谷胱甘肽 S-转移酶(GST))的创新解决方案受到了关注。二聚黄酮类化合物,尤其是双链脲类(BRAs),已证明具有多种生物活性,包括抗寄生虫作用。本研究的目的是从Fridericia platyphylla根中分离出四种二聚黄酮类化合物,并评估它们作为R. microplus GST抑制剂的潜力:体外试验证实,BRA-G、BRA-I、BRA-J 和 BRA-K 对 R. microplus GST 具有抑制作用,其 IC50 值分别为 0.075、0.079、0.075 和 0.058 mg/mL,且溶血作用极小。将 BRA-G、BRA-I、BRA-J 和 BRA-K 与 R. microplus GST 的三维模型进行分子对接,发现预测的相互作用 MolDock 得分分别为 -142.537、-126.831、-108.571 和 -123.041。硅学和体外分析表明,双氢脒是 R. microplus GST 的潜在抑制剂:本研究的结果加深了我们对蜱体内 GST 抑制作用的了解,肯定了其作为药物靶点的可行性。这些知识有助于改进蜱虫控制的治疗方法和策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Medicinal Chemistry
Medicinal Chemistry 医学-医药化学
CiteScore
4.30
自引率
4.30%
发文量
109
审稿时长
12 months
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.
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