ANTIMICROBIAL, CYTOTOXIC, AND ENZYME INHIBITORY ACTIVITIES OF Garcinia mangostana L. PERICARP EXTRACT RELEVANT TO DIABETES AND ALZHEIMER’S DISEASE: FINDINGS FROM AN IN VITRO STUDY | Hiền | TNU Journal of Science and Technology

ANTIMICROBIAL, CYTOTOXIC, AND ENZYME INHIBITORY ACTIVITIES OF Garcinia mangostana L. PERICARP EXTRACT RELEVANT TO DIABETES AND ALZHEIMER’S DISEASE: FINDINGS FROM AN IN VITRO STUDY

About this article

Received: 12/05/25                Revised: 14/08/25                Published: 14/08/25

Authors

1. Nguyen Thi Hien, University of Economics - Technology for Industries
2. Nguyen Thi Hong Hanh Email to author, Hanoi National University of Education

Abstract


This study evaluated the antimicrobial activity, enzyme inhibition (of α-glucosidase and acetylcholinesterase), and in vitro cytotoxicity of the crude extract from mangosteen (Garcinia mangostana L.) pericarp. The antimicrobial activity was assessed against seven Gram-positive, Gram-negative bacterial, and yeast microbial strains. The half maximal inhibitory concentration (IC₅₀) values of α-glucosidase and acetylcholinesterase inhibition were determined using interpolation methods with TableCurve software. Cytotoxicity was evaluated on Vero and HEK293 cell lines. The extract exhibited selective antibacterial activity against Gram-positive bacteria (Staphylococcus aureus, Lactobacillus fermentum, and Bacillus subtilis) with minimum inhibitory concentration values ranging from 4 to 16 µg/mL and IC₅₀ < 10 µg/mL. In enzyme inhibition assays, the extract showed moderate inhibitory activity with IC₅₀ values of 99.37 µg/mL for α-glucosidase and 83.20 µg/mL for acetylcholinesterase, higher than reference drugs but still within a biologically active range. Cytotoxicity assays revealed IC₅₀ values of 64.97 µg/mL on Vero cells and 53.42 µg/mL on HEK293 cells. Overall, the mangosteen pericarp extract demonstrated notable biological activity and acceptable cellular safety, suggesting its potential as a natural therapeutic candidate for the supportive treatment of microbial infections, metabolic disorders, and neurodegenerative diseases. Further in-depth studies on molecular mechanisms and in vivo efficacy are required to validate its clinical applicability.

Keywords


Garcinia mangostana L.; Antimicrobial activity; α-glucosidase; Acetylcholinesterase; Cytotoxicity

References


[1] D. Obolskiy, I. Pischel, N. Siriwatanametanon, and M. Heinrich, “Garcinia mangostana L.: a phytochemical and pharmacological review,” Phytotherapy Research: An International Journal Devoted to Pharmacological and Toxicological Evaluation of Natural Product Derivatives, vol. 23, no. 8, pp. 1047-1065, 2009.

[2] J. Pedraza-Chaverri, N. Cárdenas-Rodríguez, M. Orozco-Ibarra, and J. M. Pérez-Rojas, “Medicinal properties of mangosteen (Garcinia mangostana),” Food and chemical toxicology, vol. 46, no. 10, pp. 3227-3239, 2008.

[3] I. Ahmad, “Recent insight into the biological activities of synthetic xanthone derivatives,” European Journal of Medicinal Chemistry, vol. 116, pp. 267-280, 2016.

[4] K. Matsumoto, Y. Akao, E. Kobayashi et al., “Induction of apoptosis by xanthones from mangosteen in human leukemia cell lines,” Journal of Natural Products, vol. 66, no. 8, pp. 1124-1127, 2003.

[5] A. F. Majdalawieh, T. M. Terro, S. H. Ahari, and I. A. Abu-Yousef, “α-Mangostin: A Xanthone Derivative in Mangosteen with Potent Anti-Cancer Properties,” Biomolecules, vol. 14, no. 11, 2024, Art. no. 1382.

[6] K. L. Ong, L. K. Stafford, S. A. McLaughlin et al., “Global, regional, and national burden of diabetes from 1990 to 2021, with projections of prevalence to 2050: A systematic analysis for the Global Burden of Disease Study 2021,” The Lancet, vol. 402, no. 10397, pp. 203-234, 2023.

[7] E. Giacobini, “Cholinergic function and Alzheimer's disease,” International Journal of Geriatric Psychiatry, vol. 18, no. S1, pp. S1-S5, 2003.

[8] L. A. Profenno, A. P. Porsteinsson, and S. V. Faraone, “Meta-analysis of Alzheimer's disease risk with obesity, diabetes, and related disorders,” Biological Psychiatry, vol. 67, no. 6, pp. 505-512, 2010.

[9] M. Alssema, C. Ruijgrok, E. E. Blaak et al., “Effects of alpha-glucosidase-inhibiting drugs on acute postprandial glucose and insulin responses: A systematic review and meta-analysis,” Nutrition & diabetes, vol. 11, no. 1, pp. 11-19, 2021.

[10] K. Sharma, “Cholinesterase inhibitors as Alzheimer's therapeutics,” Molecular Medicine Reports, vol. 20, no. 2, pp. 1479-1487, 2019.

[11] J. A. Hendrix, R. J. Bateman, H. R. Brashear et al., “Challenges, solutions, and recommendations for Alzheimer's disease combination therapy,” Alzheimer's & Dementia, vol. 12, no. 5, pp. 623-630, 2016.

[12] T. H. Nguyen, T. H. H. Nguyen, T. N. Tran, and H. P. Cao “Assessment of acute oral toxicity and minimum inhibitory concentration against yogurt fermentation microbial strains of ethanol extract and alpha-mangostin-rich extract from mangosteen (Garcinia mangostana L.) pericarp,” in Proceeding of the 6th National Scientific Conference on Biological Research and Teaching in Vietnam. Natural Science and Technology Publishing House, 2024, pp. 871-881.

[13] T. Mosman, “Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assay,” J. Immunol. Method., vol. 65, pp. 55-63, 1983.

[14] D. A. Scudiero, R. H. Shoemaker, D. P. Kenneth, et al., “Evaluation of a soluable tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines,” Cancer Reseach, vol. 48, pp. 4827-4833, 1988.

[15] W. Hakamata, M. Kurihara, H. Okuda, et al., “Design and screening strategies for α-glucosidase inhibitors based on enzymological information,” Current Topics in Medicinal Chemistry, vol. 9, no. 1, pp. 3-12, 2009.

[16] G. L. Ellman, K. D. Courtney, V. Andres, et al., "A new and rapid colorimetric determination of acetylcholinesterase activity," Biochemical Pharmacology, vol. 7, pp. 88-95, 1961.

[17] G. Somani, C. Kulkarni, P. Shinde, et al.,In vitro acetylcholinesterase inhibition by psoralen using molecular docking and enzymatic studies,” J. Pharm Bioallied Sci., vol. 7, no. 1, pp. 32-36, 2015.

[18] N. H. Tran and N. L. Nguyen, “Antimicrobial activity from the extract of the pericarp of Lai Thieu mangosteen (Garcinia mangostana),” (in Vietnamese), Can Tho University Journal of Science, vol. 57, no. 1B, pp. 93-98, 2021.

[19] T. T. Do, T. H. Mai, T. M. Phi, et al., “Investigation on antibacterial activity of alpha-mangostin from the fruit hulls of Garcinia mangostana L.,” (in Vietnamese), Journal of Science and Technology – Industrial University of Ho Chi Minh City, vol. 50, no. 1, pp. 21-28, 2012.

[20] R. Watanapokasin, F. Jarinthanan, Y. Nakamura, et al., “Effects of α-mangostin on apoptosis induction of human colon cancer,” World Journal of Gastroenterology: WJG, vol. 17, no. 16, 2011, Art. no. 2086.

[21] A. M. Omar, D. F. AlKharboush, K. A. Mohammad, et al., “Mangosteen metabolites as promising alpha-amylase inhibitor candidates: in silico and in vitro evaluations,” Metabolites, vol. 12, no. 12, pp. 1229-1247, 2022.

[22] K. Y. Khaw, S. B. Choi, S. C. Tan, H. A. Wahab, K. L. Chan, and V. Murugaiyah, “Prenylated xanthones from mangosteen as promising cholinesterase inhibitors and their molecular docking studies,” Phytomedicine, vol. 21, no. 11, pp. 1303-1309, 2014.




DOI: https://doi.org/10.34238/tnu-jst.12780

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