Withanolides from Withania somnifera as an immunity booster and their therapeutic options against COVID-19
Khanal P, Chikhale R, Dey YN, Pasha I, Chand S, Gurav N, Ayyanar M, Patil BM, Gurav S
Journal of biomolecular structure & dynamics · 37 citations
Review labels
Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.
How it was studied
- Design
- In vitro/mechanistic study (classified by our AI screen)
- Studied in
- Cells or lab samples
- Main outcome
- Mechanisms only
Who paid for it
- Funding
- Funding not disclosed
Publication
- Published
- 2021-01-18 · J Biomol Struct Dyn · vol. 40 · issue 12 · pp. 5295–5308
- Publisher
- Taylor & Francis
- Cited
- 64 citations · more than 98% of similar papers · 7.6× the field average
- Impact
- Top 10% most cited in its field
- References
- 52 works
- Access
- Paywalled
- Research areas
- Computational Drug Discovery Methods · Phytochemicals and Medicinal Plants · Diverse Scientific Research Studies
- Keywords
- Withanolide, Withania somnifera, Withaferin A, Chemistry, Biology, Biochemistry, Medicine
- MeSH
- humans, withania, withanolides, spike glycoprotein, coronavirus, covid-19 drug treatment
9 authors
From IN, GB, ER
- Pukar KhanalKLE Academy of Higher Education and Research
- Rupesh V. ChikhaleUniversity of East Anglia
- Yadu Nandan DeyAdamas University
- Ismail PashaUniversity of Asmara
- Sharad ChandNitte University
- Nilambari S. GuravGoa University
Abstract
Traditionally, Withania somnifera is widely used as an immune booster, anti-viral, and for multiple medicinal purposes. The present study investigated the withanolides as an immune booster and anti-viral agents against the coronavirus-19. Withanolides from Withania somnifera were retrieved from the open-source database, their targets were predicted using DIGEP-Pred, and the protein-protein interaction was evaluated. The drug-likeness score and intestinal absorptivity of each compound were also predicted. The network of compounds, proteins, and modulated pathways was constructed using Cytoscape, and docking was performed using autodock4.0, and selected protein-ligand complexes were subjected to 100 ns Molecular Dynamics simulations. The molecular dynamics trajectories were subjected to free energy calculation by the MM-GBSA method. Withanolide_Q was predicted to modulate the highest number of proteins, showed human intestinal absorption, and was predicted for the highest drug-likeness score. Similarly, combined network interaction identified Withanolide_Q to target the highest number of proteins; RAC1 was majorly targeted, and fluid shear stress and atherosclerosis associated pathway were chiefly regulated. Similarly, Withanolide_D and Withanolide_G were predicted to have a better binding affinity with PLpro, Withanolide_M with 3CLpro, and Withanolide_M with spike protein based on binding energy and number of hydrogen bond interactions. MD studies suggested Withanoside_I with the highest binding free energy (ΔGbind-31.56 kcal/mol) as the most promising inhibitor. Among multiple withanolides from W. somnifera, Withanolide_D, Withanolide_G, Withanolide_M, and Withanolide_Q were predicted as the lead hits based on drug-likeness score, modulated proteins, and docking score to boost the immune system and inhibit the COVID-19 infection, which could primarily act against COVID-19. HighlightsWithanolides are immunity boosters.Withanolides are a group of bio-actives with potential anti-viral properties.Withanolide_G, Withanolide_I, and Withanolide_M from Withania somnifera showed the highest binding affinity with PLpro, 3CLpro, and spike protein, respectively.Withanolides from Withania somnifera holds promising anti-viral efficacy against COVID-19.Communicated by Vsevolod Makeev.
Abstract via Europe PMC. Copyright remains with the authors or publisher.
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