Mangifera indica L. Extract and Mangiferin Modulate Cytochrome P450 and UDP‐Glucuronosyltransferase Enzymes in Primary Cultures of Human Hepatocytes
Abstract
The aqueous stem bark extract of Mangifera indica L. (MSBE) has been reported to have antioxidant, anti-inflammatory and analgesic properties. In previous studies, we showed that MSBE and mangiferin, its main component, lower the activity of some cytochrome P-450 (P450) enzymes in rat hepatocytes and human liver microsomes. In the present study, the effects of MSBE and mangiferin on several P450 enzymes and UDP-glucuronosyltransferases (UGTs) in human-cultured hepatocytes have been examined. After hepatocytes underwent a 48-h treatment with sub-cytotoxic concentrations of the products (50-250 µg/mL), a concentration-dependent decrease of the activity of the five P450 enzymes measured (CYP1A2, 2A6, 2C9, 2D6 and 3A4) was observed. For all the activities, a reduction of at least 50% at the highest concentration (250 µg/mL) was observed. In addition, UGT activities diminished. MSBE considerably reduced UGT1A9 activity (about 60% at 250 µg/mL) and lesser effects on the other UGTs. In contrast, 250 µg/mL mangiferin had greater effects on UGT1A1 and 2B7 than on UGT1A9 (about 55% vs. 35% reduction, respectively). Quantification of specific mRNAs revealed reduced CYP3A4 and 3A5 mRNAs content, and an increase in CYP1A1, CYP1A2, UGT1A1 and UGT1A9 mRNAs. No remarkable effects on the CYP2A6, 2B6, 2C9, 2C19, 2D6 and 2E1 levels were observed. Our results suggest that the activity and/or expression of major P450 and UGT enzymes is modulated by MSBE and that potential herb-drugs interactions…
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Material standardization is uneven, with frequent use of extracts or nanoparticles without full reporting of purity, content uniformity, or release profiles.
“Material standardization is uneven, with frequent use of extracts or nanoparticles without full reporting of purity, content uniformity or release profiles, making cross-study comparisons difficult and weakening conclusions regarding the active entity (161,181).”
From Mangiferin in human disease: Multifaceted mechanisms and applications (Review) (2026) · cites this paper as [181]
Evaluation of drug-drug interaction risks for MGF is sparse.
“ii) sparse evaluation of drug-drug interaction risks given pathway cross-talk (for example, with PI3K/Akt, AMPK or NF-κB modulators) (181-183)”
From Mangiferin in human disease: Multifaceted mechanisms and applications (Review) (2026) · cites this paper as [181]
Cites
Guha, S., Ghosal, S., & Chattopadhyay, U. (2009) · Chemotherapy · doi:10.1159/000239478 · Cited by 275 · cited 2× · see citing works
“The pharmacological actions of mangiferin include antioxidant, analgesic (Dar et al., 2005), antidiabetic (Ichiki et al., 1998), anti-inflammatory (Ojewole, 2005), antitumor, immunomodulatory and anti-HIV effects (Guha et al., 1996).”
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Sarfraz, M., Khan, A., Batiha, G. E.-S., Akhtar, M. F., Saleem, A., Ajiboye, B. O., Kamal, M., Ali, A., Alotaibi, N. M., Aaghaz, S., et al. (2023) · Cancers · doi:10.3390/cancers15164194 · Cited by 20 · see citing works
Mangiferin in human disease: Multifaceted mechanisms and applications (Review)
Dai, Y., Huang, Q., Tan, M., Wang, Z., Jiang, C., Liu, Z., Zhang, S., & Song, S. (2026) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2026.5736 · Cited by 3 · see citing works
“Material standardization is uneven, with frequent use of extracts or nanoparticles without full reporting of purity, content uniformity or release profiles, making cross‑study comparisons difficult and weakening conclusions regarding the active entity (161,181).”
- Authors
- Rodeiro, I., José Gómez‐Lechón, M., Perez, G., Hernandez, I., Herrera, J. A., Delgado, R., Castell, J. V., & Teresa Donato, M.
- Affiliations
- Departamento de Farmacología Centro de Bioproductos Marinos (CEBIMAR) Loma 37, Vedado 10400 Havana Cuba
- Unidad de Hepatología Experimental Centro de Investigación, Hospital La Fe Avda Campanar 21 46009 Valencia Spain
- University of Havana (CU)
- Laboratorio Farmacología Molecular Centro de Investigación y Desarrollo de Medicamentos, 26 y 51 Plaza de la Revolución 10400 Havana Cuba
- Universitat de València (ES)
- Corresponding author
- Rodeiro, Idania
- Venue
- Phytotherapy Research
- Publisher
- Wiley
- Published
- 2012-07-20
- Volume
- 27
- Issue
- 5
- Pages
- 745-752
- ISSN
- 0951-418X (ISSN-L)
- 1099-1573
- OpenAlex
- W1849883515
- Cited by
- 29
- References
- 1
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 1 · 2023: 2 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 3 · 2018: 5 · 2017: 1 · 2016: 2 · 2015: 3 · 2013: 2
- FWCI
- 3.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Phytotherapy Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Complementary and alternative medicine › Mangiferin and Mango Extracts
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Keywords
- mango, mangiferin, stem bark extract, cytochrome P450, UDP-glucuronosyltransferase, human hepatocytes, drug-metabolizing enzymes, herb-drug interactions, CYP3A4, UGT1A9, UGT1A1, CYP1A2, gene expression, ADMET properties
- MeSH terms
- Cells, Cultured, Cytochrome P-450 Enzyme System, Humans, Plant Extracts, Glucuronosyltransferase, Hepatocytes, Plant Bark, Mangifera
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