评价西尔维斯特醇作为儿童COVID-19潜在治疗剂:一种解释计算和植物化学方法

IF 4.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2025-09-17 eCollection Date: 2025-01-01 DOI:10.3389/fphar.2025.1673591
Yi Zhang, Shanshan Pu, Hui Wang
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引用次数: 0

摘要

背景:由SARS-CoV-2诱导的持续性COVID-19疾病引发了对儿科患者现有治疗方法安全性和有效性的巨大质疑。目前用于治疗COVID-19的抗病毒药物,无论是瑞德西韦还是单克隆抗体,主要是为成人设计的。在许多情况下,由于对安全和儿科人口的担忧,它们的发展受到阻碍。目的:在本研究中,我们考虑从大戟中提取的天然产物西尔维斯特罗作为儿童COVID-19的潜在治疗方法。方法:分子对接研究表明,希尔维斯特罗与SARS-CoV-2刺突蛋白受体结合域(RBD)具有-7.5 kcal/mol的高度竞争性结合亲和力,表明其可能抑制病毒进入。为了进一步了解这种相互作用的动力学,进行了分子动力学(MD)模拟,证明了蛋白质在150ns内稳定,而配体则发生构象变化以适应结合袋,并最终稳定。药效团的表征还揭示了重要的相互作用点,包括4个氢键供体、12个氢键受体和8个疏水位点,这些相互作用点增加了药效团的结合潜力。结果:良好的ADMET分析预测了西威司罗的药代动力学特性,具有体外和体内的肿瘤杀伤特性,LD50为2300 mg/kg(毒性5),具有较高的安全边际。大多数西尔维斯特醇的毒性终点可能是无活性的;但可能存在免疫毒性和营养毒性,有待进一步研究。通过DFT分析得到其合理值0.20606 eV,证实了其抗病毒相互作用的反应性。结论:观察结果表明,西尔维斯特罗具有强效抗病毒、低毒性和良好的药代动力学,是治疗儿童COVID-19的有希望的药物。需要进一步的临床前和临床试验来证明其在儿童中的有效性和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of silvestrol as a potential therapeutic agent for pediatric COVID-19: an interpreted computational and phytochemistry approach.

Background: The persistent COVID-19 disease, induced by SARS-CoV-2, sparked great questions about the safety and efficacy of the existing therapies in pediatric patients. The currently available antiviral drugs for treating COVID-19, either remdesivir or monoclonal antibodies, are primarily designed for adults. In many cases, their development has been hindered by concerns about safety and pediatric populations.

Objectives: In the present study, we consider Silvestrol, a natural product derived from Euphorbia hirta, as a potential treatment for pediatric COVID-19.

Methods: The molecular docking studies revealed that Silvestrol exhibits a highly competitive binding affinity of -7.5 kcal/mol with the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein, indicating that it may inhibit viral entry. In order to learn more about the dynamics of this interaction, the molecular dynamics (MD) simulations were carried out, which proved that the protein was stabilized in 150 ns, whereas the ligand showed conformational changes to be fit in the binding pocket, and finally stabilizing. The characterization of the pharmacophore also revealed important interaction points, including four hydrogen bond donors, 12 hydrogen bond acceptors, and eight hydrophobic sites, which increase its binding potential.

Results: The favorable ADMET analysis predicted the pharmacokinetic properties of Silvestrol, which exhibited tumor-killing characteristics in vitro and in vivo activities, and an LD50 of 2,300 mg/kg (toxicity 5), implying a high safety margin. Most toxicity endpoints of Silvestrol were likely to be inactive; however, there was a chance of immunotoxicity and nutritional toxicity, which require further investigation. Its reactivity in antiviral interactions has been confirmed by its reasonable value of 0.20606 eV obtained through the DFT analysis.

Conclusion: The observations suggest that Silvestrol is a promising agent for treating COVID-19 in children, as it exhibits a potent antiviral effect, low toxicity, and favorable pharmacokinetics. Further preclinical and clinical testing is needed to demonstrate its effectiveness and safety in children.

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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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