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dc.contributor.authorZubaidi, Siti Norliyana
dc.contributor.authorQadi, Wasim S. M.
dc.contributor.authorMaarof, Syahida
dc.contributor.authorHellal, Khaoula
dc.date.accessioned2023-09-15T12:27:17Z
dc.date.available2023-09-15T12:27:17Z
dc.date.issued2023en_US
dc.identifier.citationZubaidi, S.N.; Qadi, W.S.M.; Maarof, S.; Mohmad Misnan, N.; Mohammad Noor, H.S.; Hamezah, H.S.; Baharum, S.N.; Rosli, N.; Jam, F.A.; Al-Olayan, E.; et al. Assessing the Acute Toxicological Effects of Annona muricata Leaf Ethanol Extract on Rats: Biochemical, Histopathological, and Metabolomics Analyses. Toxics 2023, 11, 688. https://doi.org/10.3390/toxics11080688en_US
dc.identifier.issn2305-6304
dc.identifier.urihttps://doi.org/10.3390/toxics11080688
dc.identifier.urihttps://hdl.handle.net/20.500.12809/10964
dc.description.abstractAnnona muricata is a common plant used in Africa and South America to manage various types of disease. However, there is insufficient toxicological information or published standard available regarding repeated dose animal toxicity data. As part of the safety assessment, we exposed Sprague Dawley rats to an acute oral toxicity of A. muricata. The intent of the current study was to use advanced proton nuclear magnetic resonance (H-1 NMR) in serum and urinary metabolomics evaluation techniques to provide the in vivo acute toxicological profile of A. muricata leaf ethanol extract in accordance with the Organization for Economic Co-operation and Development's (OECD) 423 guidelines. A single 2000 mg/kg dose of A. muricata leaf ethanol extract was administered to Sprague Dawley rats over an observational period of 14 days. The toxicity evaluation (physical and behavior observation, body weight, renal function test, liver function test and H-1 NMR analysis) showed no abnormal toxicity. Histopathological analysis manifested mild changes, i.e., the treated kidney manifested mild hypercellularity of mesangial cells and mild red blood cell congestion. In addition, there was mild hemorrhage into tissue with scattered inflammatory cells and mild dilated central vein with fibrosis in the liver. However, the changes were very mild and not significant which correlate with other analyses conducted in this study (biochemical test and H-1 NMR metabolomic analysis). On the other hand, urinary H-1 NMR analysis collected on day 15 revealed high similarity on the metabolite variations for both untreated and treated groups. Importantly, the outcomes suggest that A. muricata leaf ethanol extract can be safely consumed at a dose of 2000 mg/kg and the LD50 must be more than 2000 mg/kg.en_US
dc.item-language.isoengen_US
dc.publisherMDPIen_US
dc.relation.isversionof10.3390/toxics11080688en_US
dc.item-rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectA. muricataen_US
dc.subjectBiochemical testen_US
dc.subjectHistopathologyen_US
dc.subjectToxicityen_US
dc.subject1H NMR metabolomicsen_US
dc.titleAssessing the Acute Toxicological Effects of Annona muricata Leaf Ethanol Extract on Rats: Biochemical, Histopathological, and Metabolomics Analysesen_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Fen Fakültesi, Kimya Bölümüen_US
dc.contributor.authorID0000-0002-1223-271Xen_US
dc.contributor.institutionauthorHellal, Khaoula
dc.identifier.volume11en_US
dc.identifier.issue8en_US
dc.relation.journalTOXICSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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