Essential Oils of Alpinia vietnamica Rhizomes and Leaves: Chemical Composition, Cytotoxicity, α-Glucosidase Inhibition, and Molecular Docking Approach

Author:

Tra Nguyen Thanh1,Ha Nguyen Xuan2ORCID,Tuyen Nguyen Van1,Thuy Linh Nguyen Thi1,Thu Ha Nguyen Thi1,Cham Ba Thi1,Tu Anh Le Thi1,Hai Yen Le Thi3,The Son Ninh1ORCID

Affiliation:

1. Institute of Chemistry, Vietnam Academy of Science and Technology (VAST), Caugiay, Hanoi, Vietnam

2. Institute of Natural Products Chemistry, VAST, Caugiay, Hanoi, Vietnam

3. Hanoi Medical College, Dongda, Hanoi, Vietnam

Abstract

Objective: Alpinia is a big genus of flowering plants in the family Zingiberaceae. The plants of this genus are generally aromatic due to their essential oils. The current study aims to identify chemical compositions in the rhizome and leaf oils of Alpinia vietnamica H.Đ. Trần, Luu & Škorničk. Methods: Essential oils of A vietnamica rhizomes and leaves obtained by hydrodistillation were investigated by the gas chromatography–flame ionization detection/mass spectrometry (GC–FID/MS) analysis. A vietnamica essential oils have been subjected to cytotoxic and α-glucosidase inhibitory assays. The protein interactions of the major compounds were viewed by molecular docking study. Results: In general, monoterpene hydrocarbons (60.4%-62.5%) and their oxygenated derivatives (18.1%-29.0%) were the main chemical classes of the rhizome and leaf oils. In the meantime, 1,8-cineole (25.7%-29.0%), β-pinene (12.8%-21.3%), geraniol (9.0%-15.2%), and α-pinene (6.1%-7.5%) can be seen as the main compounds. A vietnamica essential oils showed cytotoxicity toward four cancer cell lines KB, Hep-G2, Lu-1, and MCF-7 with IC50 values of 82.39 to 254.1 µg/mL. Significantly, the leaf oil (IC50 115.18 µg/mL) was better than the standard compound acarbose (IC50 156.68 µg/mL) in the α-glucosidase inhibitory assay. The results of molecular docking simulation suggested that 1,8-cineole, geraniol, α-pinene, and β-pinene could generate a similar inhibition (binding affinities) with acarbose, and the hydrogen and hydrophobic interactions played contributory roles in the binding to α-glucosidase enzyme. Conclusion: Further phytochemical investigations on this species, especially chromatographic separations to isolate bioactive metabolites, are needed. As well, pharmacological experiments are welcome since the current study is the first result.

Funder

Vietnam Academy Science and Technology

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

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