Journal of Medicinal Materials, 2025, Vol. 30, No. 2 (pp. 86 - 91)

TRITERPENOID SAPONINS FROM THE ROOTS OF POLYGALA TENUIFOLIA: IN VITRO AND IN SILICO STUDY OF ACETYLCHOLINESTERASE INHIBITORY ACTIVITIES

Le Ba Vinh, Nguyen Van Chinh, Nguyen Cao Cuong*

Faculty of Medicine and Pharmacy, Yersin University of Da Lat, Lam Dong, Vietnam

*Corresponding author: nguyencaocuong2712@gmail.com

Summary

Triterpenoid Saponins from the Roots of Polygala tenuifolia: In vitro and in silico Study
of Acetylcholinesterase Inhibitory Activities

Polygala tenuifolia, known as Yuan Zhi in traditional Chinese medicine and Viễn Chí in Vietnamese medicine, is renowned for its cognitive-enhancing and anti-inflammatory properties. Phytochemical investigations of its roots have led to the isolation of four oleanane-type triterpenoid saponins (1–4). Using sophisticated analytical techniques, such as electrospray ionization mass spectrometry (ESI-MS) and both 1D and 2D nuclear magnetic resonance (NMR) spectroscopy, the structures of these compounds were elucidated. The identified compounds were polygalasaponin XXVIII (1), onjisaponin B (2), desacylsenegasaponin B (3), and platycodin D (4). The acetylcholinesterase (AChE) inhibitory activities of these compounds were tested, revealing that compound 1 exhibited an IC₅₀ value of 12.3 ± 1.6 μM, which is relatively higher than that of the positive control, tacrine (IC₅₀ = 3.2 ± 1.8 μM). To further investigate the underlying mechanisms of AChE inhibition, molecular docking studies were performed. These findings validate the potential of P. tenuifolia as an AChE inhibitor through its triterpenoid saponin constituents. However, in vivo studies are crucial to confirm its therapeutic potential and explore its clinical applications.

Keywords: Polygala tenuifolia; Triterpenoid saponin; Acetylcholinesterase inhibition.

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