Network pharmacology-based toxicity, molecular docking, and molecular dynamics analysis of phytoconstituents from roots of Nerium indicum L

• Oleandrin and odoroside A exhibit high systemic and organ-specific toxicity • Targets PTGS2 and MAPK1 disrupt inflammation and survival signaling pathways • Docking shows strong binding of oleandrin to cardiotoxicity-related proteins • GO analysis links compounds to oxidative stress and neuroinflammation • Supports detox strategies for safer therapeutic use of Nerium indicum Herbal medicine plays a vital role in healthcare, but safety concerns arise due to potential toxicity risks. Nerium indicum (夹竹桃, jiā zhú táo) is used in Chinese herbal medicine for its therapeutic effects, yet it contains toxic cardiac glycosides. This study investigates its toxicity mechanisms using systems biology tools to support safer applications through comprehensive risk-benefit evaluation and detoxification strategies. Computational analyses were performed to predict drug-likeness, toxicity, LD₅₀, and blood-brain barrier (BBB) penetration. Key toxicity-related genes were identified using SwissTargetPrediction and GeneCards. Gene Ontology (GO) and pathway enrichment analyses further explored toxicity mechanisms, while molecular docking and dynamics simulations assessed interactions between core targets, Prostaglandin-endoperoxide synthase 2 (PTGS2) and Mitogen-Activated Protein Kinase 1 (MAPK1), offering deeper insights into toxicity modulation. Computational analyses identified oleandrin, and odoroside A as highly toxic, with significant cardiotoxic and hepatotoxic risks. Network analysis revealed PTGS2 and MAPK1 as key toxicity regulators, mediating pathways linked to inflammation and cellular stress. Molecular docking showed Oleandrin exhibiting the strongest binding affinities with PTGS2 (-8.5 kcal/mol) and MAPK1 (-9.2 kcal/mol), while molecular dynamics simulations confirmed its stable interactions, suggesting a critical role in toxicity modulation. This study highlights Oleandrin and related compounds as major toxicity contributors in Nerium indicum, emphasizing their impact on cardiac, hepatic, and neurological pathways. The findings underscore the need for cautious therapeutic use and potential detoxification strategies for safer applications.

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Publication Details

Journal
Pharmacological Research - Modern Chinese Medicine
Published
2025-06-07
DOI
https://doi.org/10.1016/j.prmcm.2025.100640
Citations
4
Primary Topic
Pharmacological Effects of Natural Compounds
Type
article
Field-Weighted Citation Impact
6.23
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article

Network pharmacology-based toxicity, molecular docking, and molecular dynamics analysis of phytoconstituents from roots of Nerium indicum L

Vishal S. Patil, Anand Desai, Mrityunjaya B. Patil, Banappa S. Unger et al.
4 citations
Pharmacological Research - Modern Chinese Medicine
Pharmacological Effects of Natural Compounds
6.23
article

Network pharmacology-based toxicity, molecular docking, and molecular dynamics analysis of phytoconstituents from roots of Nerium indicum L

Vishal S. Patil, Anand Desai, Mrityunjaya B. Patil, Banappa S. Unger, Shamanand P. Mallapur, Veerkumar P. Japti, S. S. Patil, Akshay Shamnewadi
article en
4 citations

Abstract

• Oleandrin and odoroside A exhibit high systemic and organ-specific toxicity • Targets PTGS2 and MAPK1 disrupt inflammation and survival signaling pathways • Docking shows strong binding of oleandrin to cardiotoxicity-related proteins • GO analysis links compounds to oxidative stress and neuroinflammation • Supports detox strategies for safer therapeutic use of Nerium indicum Herbal medicine plays a vital role in healthcare, but safety concerns arise due to potential toxicity risks. Nerium indicum (夹竹桃, jiā zhú táo) is used in Chinese herbal medicine for its therapeutic effects, yet it contains toxic cardiac glycosides. This study investigates its toxicity mechanisms using systems biology tools to support safer applications through comprehensive risk-benefit evaluation and detoxification strategies. Computational analyses were performed to predict drug-likeness, toxicity, LD₅₀, and blood-brain barrier (BBB) penetration. Key toxicity-related genes were identified using SwissTargetPrediction and GeneCards. Gene Ontology (GO) and pathway enrichment analyses further explored toxicity mechanisms, while molecular docking and dynamics simulations assessed interactions between core targets, Prostaglandin-endoperoxide synthase 2 (PTGS2) and Mitogen-Activated Protein Kinase 1 (MAPK1), offering deeper insights into toxicity modulation. Computational analyses identified oleandrin, and odoroside A as highly toxic, with significant cardiotoxic and hepatotoxic risks. Network analysis revealed PTGS2 and MAPK1 as key toxicity regulators, mediating pathways linked to inflammation and cellular stress. Molecular docking showed Oleandrin exhibiting the strongest binding affinities with PTGS2 (-8.5 kcal/mol) and MAPK1 (-9.2 kcal/mol), while molecular dynamics simulations confirmed its stable interactions, suggesting a critical role in toxicity modulation. This study highlights Oleandrin and related compounds as major toxicity contributors in Nerium indicum, emphasizing their impact on cardiac, hepatic, and neurological pathways. The findings underscore the need for cautious therapeutic use and potential detoxification strategies for safer applications.

Pharmacological Research - Modern Chinese MedicineVol. 16
Indian Council of Medical Research (IN), KLE Academy of Higher Education and Research (IN), Krishna Institute of Medical Sciences Deemed University (IN), Academy of Scientific and Innovative Research (IN)
Zero hunger
Openalex Percentile: Top 4%
Pharmacological Effects of Natural Compounds
6.23
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