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LC–MS/MS metabolite profiling and in vivo antidiabetic, antilipidemic, and hepatoprotective potential of Ipomoea mombassana leaf extract with in silico validation

Lakshmi Rajita Kotta, A. Vijayalakshmi

Pharmaceutical Sciences Asia, 2026

Abstract

Diabetes mellitus, often associated with dyslipidemia and hepatic dysfunction, requires effective plantderived therapeutics. This study evaluated the metabolite profile and pharmacological potential of the ethanolic

leaf extract of Ipomoea mombassana Vatke (IMLE). LC-MS/MS profiling identified 37 phytochemicals,

including flavonoids, alkaloids, terpenoids, and two previously unreported compounds, zinnimidine and

cinncassiol A 19-glucoside. Molecular docking demonstrated strong inhibitory activity of key metabolites against

α-amylase, with binding energies ranging from -7.6 to -9.8 kcal/mol. Tephrosin exhibited the most favorable

binding (-9.8 kcal/mol), stabilized by hydrogen bonds with HIS305 (74.9% occupancy) and TRP59 (52.2%).

Molecular dynamics simulations (100 ns) confirmed complex stability, with protein RMSD ~0.18 nm, ligand

RMSD 0.04-0.07 nm, and average MMGBSA free energy –50.73 kcal/mol. In vivo, IMLE (200 mg/kg)

significantly reduced fasting blood glucose from 344 ± 1.6 to 180 ± 3.9 mg/dL (≈48%; p<0.001), comparable to

metformin (175 ± 7.1 mg/dL), and improved oral glucose tolerance. Dyslipidemia was corrected, with total

cholesterol reduced by 38%, triglycerides by 35%, LDL-C by 68%, and HDL-C increased by 79% (all p<0.001).

Elevated SGOT and SGPT were reduced (71 → 42 U/L; 87 → 51 U/L; p<0.001). Antioxidant markers (SOD,

CAT, GSH) increased ~3-fold, while MDA decreased ~65% (p<0.001). Histopathology confirmed reversal of

pancreatic and hepatic damage. Overall,…

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