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Elucidating the active interaction mechanism of phytochemicals withanolide and withanoside derivatives with human serum albumin

机译:阐明植物化学物质阿糖苷和阿糖苷衍生物与人血清白蛋白的相互作用机理

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摘要

Withania somnifera (Ashwagandha) is an efficient medicinal plant known in Ayurveda and Chinese medicine since ancient times, whose extracts are consumed orally as food supplement or as a health tonic owing to its several restorative properties for various CNS disorders, inflammation, tumour, stress, rheumatism etc. In this study, we have analyzed the binding interaction of four derivatives of Withania somnifera (Withanolide A, Withanolide B, Withanoside IV and Withanoside V) with HSA because of their important pharmacological properties. To unravel the binding between derivatives of Withania somnifera and HSA, fluorescence spectroscopy was used. Binding studies were further studied by molecular docking and dynamics and results confirmed greater stability upon binding of derivatives with HSA. Circular dichroism data illustrated change in the secondary structure of protein upon interaction with these derivatives, particularly the helical structure was increased and β-sheets and random coils were decreased. Furthermore, morphological and topological changes were observed using AFM and TEM upon binding of ligands with HSA indicating that HSA-withnoside/withanolide complexes were formed. All the results cumulatively demonstrate strong binding of withanosides and withanolides derivatives with serum albumin, which should further be explored to study the pharmacokinetics and pharmacodynamics of these derivatives.
机译:Withania somnifera(Ashwagandha)是一种有效的药用植物,自古以来就在阿育吠陀和中草药中广为人知,由于其对多种中枢神经系统疾病,炎症,肿瘤,压力,在这项研究中,由于其重要的药理特性,我们分析了睡茄(Withaniaide A,Withanolide B,Withanoside IV和Withanoside V)的四种衍生物(Withanolide A,Withanolide B,Withanoside IV和Withanoside V)的结合作用。为了阐明Withania催眠药和HSA之间的结合,使用了荧光光谱法。通过分子对接和动力学进一步研究了结合研究,结果证实了衍生物与HSA结合后具有更大的稳定性。圆二色性数据说明了与这些衍生物相互作用时蛋白质二级结构的变化,特别是螺旋结构增加了,β-折叠和无规卷曲减少了。此外,在配体与HSA结合后,使用AFM和TEM观察到形态学和拓扑学变化,表明形成了HSA-无糖苷/ withanolide复合物。所有结果均累积证明了山梨糖苷和withanolides衍生物与血清白蛋白的强结合,应进一步探索研究这些衍生物的药代动力学和药效学。

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