苍耳草提取物作为杀螨剂的体外生物测定及硅质药动学特性研究。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Nabi Amin, Chia-Hung Wu, Nosheen Malak, Afshan Khan, Shakir Ullah, Imtiaz Ahmad, Muazzam Ali Khan, Muhammad Naveed, Zakir Ullah, Saira Naz, Adil Khan, Chien-Chin Chen
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引用次数: 0

摘要

背景:防治蜱虫侵害的有效管理策略是必要的,因为蜱传疾病对全世界人类和动物的健康构成严重危害。本研究的目的是研究苍耳提取物对一种臭名昭著的蜱种——微头蜱的杀幼虫和杀卵性能。方法:采用浸渍法制备野田菊醇提物。然后将提取液用于成虫浸泡试验(AIT)和幼虫包试验(LPT)以评估该植物的毒性。为了阐明其作用方式,进行了分子建模和对接研究。然后进行ADMET分析以找出植物化学物质的药物相似谱。结果:采用幼虫包试验(LPT)和成虫浸渍试验(AIT)对不同剂量的提取液均有显著的死亡率和卵抑制作用。浓度为40 mg/mL时,幼虫死亡率最高(92±2.646),卵抑制率最高(77.057±2.186)。此外,通过计算其致死浓度(LC50, LC90和LC99)来确定提取物对微褐螺旋体的效价。建立了微章鱼胺受体的三维模型,对接研究表明,受体和可能的配体,尤其是黄嘌呤和黄嘌呤,相互作用良好。药物相似性和ADMET研究显示,化合物的药代动力学特征和毒性特征突出了它们作为蜱虫控制剂的潜力。分子动力学模拟进一步证明了蛋白质-配体复合物的稳定性,表明配体与靶蛋白之间的结合是一致的。结论:本研究为瘤x提取物及其化合物作为杀幼剂和杀卵剂的应用前景提供了有价值的见解,为进一步研究蜱虫防治策略奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro Bioassay and In silico Pharmacokinetic Characteristics of Xanthium strumarium Plant Extract as Possible Acaricidal Agent.

Background: Effective management strategies against tick infestations are necessary because tickborne diseases represent serious hazards to the health of humans and animals worldwide. The aim of this study was to examine the larvicidal and ovicidal properties of Xanthium strumarium extract against a notorious tick species, Rhipicephalus microplus.

Methodology: The maceration method was used to prepare the ethanolic extract of X. strumarium. The extract was then used in an adult immersion test (AIT) and larval packet test (LPT) to asses the plant's toxicity. To elucidate the mode of action, molecular modeling and docking studies were conducted. ADMET analysis was then carried out to find out the drug-likeness profiles of the plant phytochemicals.

Results: Significant death rates and egg inhibition were found at different extract doses using the larval packet test (LPT) and adult immersion test (AIT). A concentration-dependent impact was observed at a concentration of 40 mg/mL, which resulted in the maximum larval mortality (92 ± 2.646) and egg inhibition (77.057 ± 2.186). Additionally, the potency of the extract against R. microplus was determined by calculating its fatal concentrations (LC50, LC90, and LC99). A three-dimensional model of the R. microplus octopamine receptor was created, and docking studies showed that the receptor and possible ligands, most notably Xanthatin and Xanthosin, interacted well. The potential of compounds as tick control agents was highlighted by their pharmacokinetic characteristics and toxicity profiles, as revealed by drug-likeness and ADMET studies. Molecular dynamic simulations further demonstrated the stability of the protein-ligand complex, indicating the consistent association between the ligand and the target protein.

Conclusion: Overall, this study provides valuable insights into the potential use of X. strumarium extract and its compounds as larvicidal and ovicidal agents against R. microplus, paving the way for further research on tick control strategies.

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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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