Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/31967
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dc.contributor.authorUsman Ahmed-
dc.contributor.authorSivasothy, Yasodha-
dc.contributor.authorKhan, Khalid Mohammed-
dc.contributor.authorKhan, Naveed Ahmed-
dc.contributor.authorSiti Mariam Abdul Wahab-
dc.contributor.authorKhalijah Awang-
dc.contributor.authorMuhamad Aqmal Othman-
dc.contributor.authorAnwar, Ayaz-
dc.contributor.author(UniKL RCMP)-
dc.date.accessioned2025-06-05T08:02:31Z-
dc.date.available2025-06-05T08:02:31Z-
dc.date.issued2023-12-
dc.identifier.citationAhmed, U., Sivasothy, Y., Khan, K. M., Khan, N. A., Wahab, Siti Mariam Abdul Wahab,Khalijah Awang, Muhamad Aqmal Othman, & Anwar, A. (2023). Malabaricones from the fruit of Myristica cinnamomea King as potential agents agains Acanthamoeba castellanii. Acta Tropica, 248, 107033. https://doi.org/10.1016/j.actatropica.2023.107033en_US
dc.identifier.issn0001706X-
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S0001706X23002206-
dc.identifier.urihttps://ir.unikl.edu.my/jspui/handle/123456789/31967-
dc.description.abstractAcanthamoeba castellanii is an opportunistic free-living amoeba (FLA) pathogen which can cause fatal central nervous system (CNS) infection, granulomatous amoebic encephalitis (GAE) and potentially blinding ocular infection, Acanthamoeba keratitis (AK). Acanthamoeba species remain a challenging protist to treat due to the unavailability of safe and effective therapeutic drugs and their ability to protect themselves in the cyst stage. Natural products and their secondary metabolites play a pivotal role in drug discovery against various pathogenic microorganisms. In the present study, the ethyl acetate extract of Myristica cinnamomea King fruit was evaluated against A. castellanii (ATCC 50492), showing an IC50 of 45.102 ± 4.62 µg/mL. Previously, the bio-guided fractionation of the extract resulted in the identification of three active compounds, namely Malabaricones (A-C). The isolated and thoroughly characterized acylphenols were evaluated for their anti-amoebic activity against A. castellanii for the first time. Among tested compounds, Malabaricone B (IC50 of 101.31 ± 17.41 µM) and Malabaricone C (IC50 of 49.95 ± 6.33 µM) showed potent anti-amoebic activity against A. castellanii trophozoites and reduced their viability up-to 75 and 80 %, respectively. Moreover, both extract and Malabaricones also significantly (p < 0.05) inhibit the encystation and excystation of A. castellanii, while showed minimal toxicity against human keratinocyte cells (HaCaT cells) at lower tested concentrations. Following that, the explanation of the possible mechanism of action of purified compounds were assessed by detection of the state of chromatin. Hoechst/PI 33342 double staining showed that necrotic cell death occurred in A. castellanii trophozoites after 8 h treatment of Malabaricones (A-C). These findings demonstrate that Malabaricones B and C could serve as promising therapeutic options against A. castellanii infections.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectAcanthamoebaen_US
dc.subjectAcylphenolsen_US
dc.subjectMalabaricones A-Cen_US
dc.subjectMyristica cinnamomea Kingen_US
dc.titleMalabaricones from the fruit of Myristica cinnamomea King as potential agents against Acanthamoeba castellaniien_US
dc.typeArticleen_US
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