In Silico Rationalization for Leads from Oldenlandia umbellata L. to Inhibit Multiple Molecular Targets Regulating Osteoporosis

IF 0.6 4区 医学 Q4 CHEMISTRY, MEDICINAL Pharmacognosy Magazine Pub Date : 2023-10-17 DOI:10.1177/09731296231196189
Sivasakthi Paramasivam, Senthamil Selvan Perumal
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Abstract

Background Osteoporosis is a chronic metabolic bone disease caused due to the dysregulation in the functioning of osteoblast and osteoclast cells leading to increased bone resorption predominantly in postmenopausal women and the elderly, thereby affecting a significant global population. Purpose The present study aims to computationally screen the phytochemical constituents of Oldenlandia umbellata Linn against the unique molecular therapeutic targets of osteoporosis and validate the results using Molecular Dynamics (MD) Simulation. Methods The molecular docking analysis of the selected phytoconstituents against the molecular targets were performed using AutoDock 4.2.6 – AutoDock Tools 1.5.6. In addition, the drug likeliness, ADME, bioactivity, and toxicity were predicted using Molinspiration ADMELAB2.0, ProTox-II and Orisis DataWarrior online tools. Molecular Dynamic Simulation studies were performed using WebGRO macromolecular simulation server. Results Molecular docking results and data analysis revealed that deacetylasperuloside possesses good drug-likeness, ADME properties, and bioactive scores and did not indicate any toxicity compared to other phytochemicals exhibiting binding energies below –8.00 Kcal/mol against the targets. Together, the study emphasized that deacetylasperuloside could bind with the molecular targets of osteoporosis, and the lead is a potential therapeutic candidate for osteoporosis treatment. Further, molecular dynamic simulation analysis for 100 ns revealed that the ligand–protein complexes, including glycogen synthase kinase 3β (GSK3β)-deacetylasperuloside and cathepsin K (CTSK)-deacetylasperuloside complexes, were stable and highly compact assessed from their trajectories. Hence, it can be emphasized that deacetylasperuloside could be a potential therapeutic molecule that could inhibit the targets, including GSK3β and CTSK. Conclusion Oldenlandia umbellata L. is a potential candidate for identifying therapeutic leads for osteoporosis treatment. Further, in vitro and in vivo studies are needed as an output of this research to evaluate its therapeutic efficacy.
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大黄铅抑制调节骨质疏松的多个分子靶点的硅理顺研究
骨质疏松症是一种慢性代谢性骨病,由于成骨细胞和破骨细胞功能失调导致骨吸收增加,主要发生在绝经后妇女和老年人中,因此影响了全球大量人群。目的利用分子动力学(molecular Dynamics, MD)模拟技术,对大黄叶的化学成分进行计算筛选,以对抗骨质疏松症的独特分子治疗靶点。方法采用AutoDock 4.2.6 - AutoDock Tools 1.5.6软件对所选植物成分与分子靶点进行分子对接分析。此外,使用Molinspiration ADMELAB2.0、ProTox-II和Orisis DataWarrior在线工具预测药物的药物可能性、ADME、生物活性和毒性。使用WebGRO大分子模拟服务器进行分子动力学模拟研究。结果分子对接结果和数据分析表明,与其他结合能低于-8.00 Kcal/mol的植物化学物质相比,去乙酰甲葡糖苷具有良好的药物相似性、ADME特性和生物活性评分,对靶标没有毒性。综上所述,该研究强调去乙酰甲葡糖苷可以结合骨质疏松症的分子靶点,该先导物是治疗骨质疏松症的潜在候选药物。此外,100 ns的分子动力学模拟分析表明,配体蛋白复合物,包括糖原合成酶激酶3β (GSK3β)-去乙酰甲葡糖苷和组织蛋白酶K (CTSK)-去乙酰甲葡糖苷复合物,从它们的轨迹评估是稳定和高度紧密的。因此,可以强调,去乙酰甲葡糖苷可能是一种潜在的治疗分子,可以抑制GSK3β和CTSK等靶点。结论大黄是鉴别骨质疏松症治疗线索的潜在候选植物。此外,需要体外和体内研究作为本研究的输出,以评估其治疗效果。
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
Pharmacognosy Magazine
Pharmacognosy Magazine CHEMISTRY, MEDICINAL-
CiteScore
1.87
自引率
0.00%
发文量
37
审稿时长
3 months
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