Byregowda Bharath Harohalli, Baby Krishnaprasad, Maity Swastika, Nayak Usha Yogendra, S Gayathri, Fayaz Shaik Mohammad, Nayak Yogendra
Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.
Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, 576194, India.
F1000Res. 2024 Jun 25;13:216. doi: 10.12688/f1000research.142513.1. eCollection 2024.
Idiopathic pulmonary fibrosis (IPF) is a disease with high mortality, and there are only two specific drugs available for therapeutic management with limitations. The study aims to identify comprehensive therapeutic mechanisms of rhizomes (ZZR) to treat IPF by using network pharmacology followed battery of in silico studies.
The protein-protein interaction network was developed using Cytoscape to obtain core disease targets involved in IPF and their interactive molecules of ZZR. Based on the pharmacophore properties of phytomolecules from ZZR, the drug targets in IPF were explored. Protein-protein interaction network was built in Cytoscape to screen potential targets and components of ZZR. Molecular docking and dynamics were conducted as an empirical study to investigate the mechanism explored through network pharmacology in relation to the hub targets.
The network analysis conferred kaempferol derivatives that had demonstrated a promising therapeutic effect on the perturbed, robust network hubs of TGF-β1, EGFR, TNF-α, MMP2 & MMP9 reported to alter the biological process of mesenchymal transition, myofibroblast proliferation, and cellular matrix deposition in pulmonary fibrosis. The phytomolecules of ZZR act on two major significant pathways, namely the TGF-β-signaling pathway and the FOXO-signaling pathway, to inhibit IPF. Confirmational molecular docking and dynamics simulation studies possessed good stability and interactions of the protein-ligand complexes by RMSD, RMSF, rGyr, SASA, and principal component analysis (PCA). Validated molecular docking and dynamics simulations provided new insight into exploring the mechanism and multi-target effect of ZZR to treat pulmonary fibrosis by restoring the alveolar phenotype through cellular networking.
Network pharmacology and in silico studies confirm the multitargeted activity of ZZR in the treatment of IPF. Further and studies are to be conducted to validate these findings.
特发性肺纤维化(IPF)是一种死亡率很高的疾病,目前仅有两种特效药物用于治疗,但都存在局限性。本研究旨在通过网络药理学结合一系列计算机模拟研究,确定莪术根茎(ZZR)治疗IPF的综合治疗机制。
利用Cytoscape构建蛋白质-蛋白质相互作用网络,以获得IPF相关的核心疾病靶点及其与ZZR的相互作用分子。基于ZZR植物分子的药效团特性,探索IPF中的药物靶点。在Cytoscape中构建蛋白质-蛋白质相互作用网络,以筛选ZZR的潜在靶点和成分。进行分子对接和动力学研究作为实证研究,以探究通过网络药理学探索的与枢纽靶点相关的机制。
网络分析表明,山奈酚衍生物对据报道可改变肺纤维化中间充质转化、肌成纤维细胞增殖和细胞基质沉积生物学过程的TGF-β1、EGFR、TNF-α、MMP2和MMP9等受干扰的强大网络枢纽具有有前景的治疗效果。ZZR的植物分子作用于两个主要的重要信号通路,即TGF-β信号通路和FOXO信号通路,以抑制IPF。通过均方根偏差(RMSD)、均方根波动(RMSF)、回转半径(rGyr)、溶剂可及表面积(SASA)和主成分分析(PCA),验证性分子对接和动力学模拟研究表明蛋白质-配体复合物具有良好的稳定性和相互作用。经过验证的分子对接和动力学模拟通过细胞网络恢复肺泡表型,为探索ZZR治疗肺纤维化的机制和多靶点效应提供了新的见解。
网络药理学和计算机模拟研究证实了ZZR在治疗IPF中的多靶点活性。有待进一步开展研究以验证这些发现。