A computational assay for identifying millet-derived compounds that antagonize the interaction between bisphenols and estrogen-related receptor gamma.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2024-10-31 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1435254
Rajesh Kumar Pathak, Jun-Mo Kim
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引用次数: 0

Abstract

The use of Bisphenol A (BPA) and its analogs in industries, as well as the products made from them, is becoming a significant concern for human health. Scientific studies have revealed that BPA functions as an endocrine disruptor. While some analogs of BPA (bisphenols) have been used for a longer time, it was later discovered that they are toxic, similar to BPA. Their widespread use ensures their presence in the environment, and thus, everyone is exposed to them. Scientific research has shown that BPA interacts with estrogen-related receptor gamma (ERRγ), affecting its normal function. ERRγ is involved in biological processes including energy metabolism and mitochondrial function. Therefore, continuous exposure to bisphenols increases the risk of various diseases. In our previous study, we observed that some analogs of BPA had a higher binding affinity to ERRγ compared to BPA itself and analyzed the amino acid residues involved in this interaction. We hypothesized that by antagonizing the interaction between bisphenols and ERRγ, we could neutralize their toxic effects. Taking into account the health benefits of millets and their toxin removal properties, virtual screening of millet-derived compounds was conducted along with prediction of their ADMET profiles. Top five candidates were prioritized for Density Functional Theory (DFT) calculations and further analyses. Long-term molecular dynamics simulation (1 µs) were utilized to evaluate their binding, stability, and antagonizing abilities. Furthermore, reevaluation of their binding energy was conducted using the MM-PBSA method. This study reports millet-derived compounds, namely, Tricin 7-rutinoside, Tricin 7-glucoside, Glucotricin, Kaempferol, and Setarin. These compounds are predicted to be potent competitive inhibitors that can antagonize the interactions between bisphenols and ERRγ. These compounds could potentially assist in the development of future therapeutics. They may also be considered for use as food supplements, although further investigations, including wet-lab experiments and clinical studies, are needed.

一种用于鉴定可拮抗双酚与雌激素相关受体 gamma 之间相互作用的小米衍生化合物的计算测定法。
双酚 A(BPA)及其类似物在工业中的使用以及由其制成的产品正成为人类健康的一个重大问题。科学研究表明,双酚 A 具有干扰内分泌的功能。虽然双酚 A 类似物(双酚)的使用时间较长,但后来发现它们与双酚 A 类似,都具有毒性。它们的广泛使用确保了它们在环境中的存在,因此,每个人都会接触到它们。科学研究表明,双酚 A 会与雌激素相关受体γ(ERRγ)相互作用,影响其正常功能。ERRγ参与能量代谢和线粒体功能等生物过程。因此,持续接触双酚会增加罹患各种疾病的风险。在之前的研究中,我们观察到与双酚 A 相比,双酚 A 的一些类似物与ERRγ 有更高的结合亲和力,并分析了参与这种相互作用的氨基酸残基。我们假设,通过拮抗双酚与ERRγ之间的相互作用,可以中和它们的毒性作用。考虑到小米对健康的益处及其清除毒素的特性,我们对小米衍生化合物进行了虚拟筛选,并预测了它们的 ADMET 特征。排在前五位的候选化合物将优先进行密度泛函理论(DFT)计算和进一步分析。利用长期分子动力学模拟(1 µs)来评估它们的结合力、稳定性和拮抗能力。此外,还使用 MM-PBSA 方法对它们的结合能进行了重新评估。本研究报告了小米衍生化合物,即三尖杉素 7-芸香糖苷、三尖杉素 7-葡萄糖苷、葡萄糖三尖杉素、山柰酚和 Setarin。据预测,这些化合物是有效的竞争性抑制剂,可以拮抗双酚和ERRγ之间的相互作用。这些化合物可能有助于未来治疗药物的开发。尽管还需要进一步的研究,包括湿实验室实验和临床研究,但它们也可以考虑用作食品补充剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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