IN VIVO AND NETWORK PHARMACOLOGY BASED MOLECULAR SCREENING OF POTENTIAL COMPOUNDS FROM CASSIA ABSUS SEEDS AGAINST HYPERLIPIDEMIA

Background: Medicinal plants are valuable sources of bioactive chemicals with multi-target effects. Cassia absus, traditionally used to treat various ailments such as conjunctivitis, tumours, and hepatic disorders, was investigated for its anti-hyperlipidemic potential—a major risk factor for hypertension and cardiovascular diseases. Objectives: To prepare C. absus seeds extract in methanol and measure their efficacy against hyperlipidemia in selected rat groups. To identify the bioactive, drug-like compounds using network pharmacology and molecular docking. Methodology: Rats were divided into four groups: control on a normal diet (T0), hyperlipidemic group on a fat-rich diet (T1), atorvastatin-treated group (T2), and seeds extract-treated group (T3). Lipid levels were measured on days 0, 7 and 14. Active compounds in C. absus seeds were identified using databases and screened for drug-likeness by Lipinski's Rule and Swiss ADME. Swiss TargetPrediction, GeneCards and NCBI identified compounds and disease-targeted genes. Compounds-target interacting genes were identified via Venn diagram. Protein-protein interaction created by STRING, DAVID provided functional gene annotations and KEGG Pathways. Compound-target-pathway networks visualized using Cytoscape, with molecular docking predicted binding affinity. Results: The T3 group showed a significant improvement in lipid profile, with a reduction in TC (47.2%), triglycerides (53.4%), LDL (61.7%), and an elevated HDL (51.5%). A study identified six anti-hyperlipidemic compounds, including 4,6-dimethyl mannose, methyl gallate, and syringic acid. Strong binding affinity observed between ALB1, PPARG, and ESR1 proteins. Most interacting disease-targeted pathways were also identified. Conclusion: The study supported the anti-hyperlipidemic potential of C. absus seeds and their drug-like compounds through network pharmacology, thus paving the way for the development of herbal medicine.

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Journal
International Journal of Pharmacy & Integrated Health Sciences
Published
2025-08-28
DOI
https://doi.org/10.56536/ijpihs.v6i2.280
Primary Topic
Phytochemistry and biological activity of medicinal plants
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article
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article

IN VIVO AND NETWORK PHARMACOLOGY BASED MOLECULAR SCREENING OF POTENTIAL COMPOUNDS FROM CASSIA ABSUS SEEDS AGAINST HYPERLIPIDEMIA

Muhammad Nadeem Abbas, Niaz Muhammad, A. Chaudary, S MEHBOOB
International Journal of Pharmacy & Integrated Health Sciences
Phytochemistry and biological activity of medicinal plants
article

IN VIVO AND NETWORK PHARMACOLOGY BASED MOLECULAR SCREENING OF POTENTIAL COMPOUNDS FROM CASSIA ABSUS SEEDS AGAINST HYPERLIPIDEMIA

Muhammad Nadeem Abbas, Niaz Muhammad, A. Chaudary, S MEHBOOB
article en

Abstract

Background: Medicinal plants are valuable sources of bioactive chemicals with multi-target effects. Cassia absus, traditionally used to treat various ailments such as conjunctivitis, tumours, and hepatic disorders, was investigated for its anti-hyperlipidemic potential—a major risk factor for hypertension and cardiovascular diseases. Objectives: To prepare C. absus seeds extract in methanol and measure their efficacy against hyperlipidemia in selected rat groups. To identify the bioactive, drug-like compounds using network pharmacology and molecular docking. Methodology: Rats were divided into four groups: control on a normal diet (T0), hyperlipidemic group on a fat-rich diet (T1), atorvastatin-treated group (T2), and seeds extract-treated group (T3). Lipid levels were measured on days 0, 7 and 14. Active compounds in C. absus seeds were identified using databases and screened for drug-likeness by Lipinski's Rule and Swiss ADME. Swiss TargetPrediction, GeneCards and NCBI identified compounds and disease-targeted genes. Compounds-target interacting genes were identified via Venn diagram. Protein-protein interaction created by STRING, DAVID provided functional gene annotations and KEGG Pathways. Compound-target-pathway networks visualized using Cytoscape, with molecular docking predicted binding affinity. Results: The T3 group showed a significant improvement in lipid profile, with a reduction in TC (47.2%), triglycerides (53.4%), LDL (61.7%), and an elevated HDL (51.5%). A study identified six anti-hyperlipidemic compounds, including 4,6-dimethyl mannose, methyl gallate, and syringic acid. Strong binding affinity observed between ALB1, PPARG, and ESR1 proteins. Most interacting disease-targeted pathways were also identified. Conclusion: The study supported the anti-hyperlipidemic potential of C. absus seeds and their drug-like compounds through network pharmacology, thus paving the way for the development of herbal medicine.

International Journal of Pharmacy & Integrated Health SciencesVol. 6(2)
Minhaj University Lahore (PK), Centre of Excellence in Molecular Biology (PK), Indiana University – Purdue University Indianapolis (US)
Openalex Percentile: Top 76%
Phytochemistry and biological activity of medicinal plants
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