Nephroprotective mechanisms of Ambrette (Abelmoschus moschatus Medik.) leaf extracts in adriamycin mediated acute kidney injury model of Wistar rats

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dc.contributor.author Amarasiri, S.S.
dc.contributor.author Attanayake, A.P.
dc.contributor.author Mudduwa, L.K.B.
dc.contributor.author Jayatilaka, K.A.P.W.
dc.date.accessioned 2022-11-15T08:54:28Z
dc.date.available 2022-11-15T08:54:28Z
dc.date.issued 2022-03-23
dc.identifier.citation Amarasiri, S.S., Attanayake, A.P., Mudduwa, L.K.B., Jayatilaka, K.A.P.W., 2022. Nephroprotective mechanisms of Ambrette (Abelmoschus moschatus Medik.) leaf extracts in adriamycin mediated acute kidney injury model of Wistar rats. Journal of Ethnopharmacology. https://doi.org/10.1016/j.jep.2022.115221 en_US
dc.identifier.issn 0378-8741
dc.identifier.uri http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/9261
dc.description.abstract Ethnopharmacological relevance: Ambrette (Abelmoschus moschatus Medik., Family: Malvaceae) is a common Ay urvedic herbal medicine used in the treatment of kidney-related diseases, in the forms of tea, medicated oil, medicated wine, etc., however, its nephroprotective mechanisms remain unexploited. Aim of the study: To investigate the mechanisms by which the hexane (A-HE), ethyl acetate (A-EE), butanol (A BE), and aqueous (A-WE) leaf extracts of Ambrette protect against the adriamycin-mediated acute kidney injury in Wistar rats. Materials and methods: A-HE, A-EE, A-BE, A-WE, and fosinopril sodium were administered at therapeutically effective doses (55, 75, 60, 140, 0.09 mg/kg) to adriamycin-induced (5 mg/kg, ip) Wistar rats for 28 consecutive days. Results: Oral administration of the selected extracts of A. moschatus resulted in amelioration of kidney injury as observed by the significant changes of biomarkers of kidney function in serum and in urine, biochemical pa rameters of oxidative stress, and inflammation in kidney homogenates (p < 0.05). Furthermore, the adminis tration of plant extracts caused a significant reduction in total kidney injury scores in H and E stained kidney sections (p < 0.05). The immunohistochemical expression of the inflammatory marker, COX-2, and the pro apoptotic marker, Bax, were attenuated and the expression of the anti-apoptotic marker, BCL-2, was increased. A-HE exerted superior nephroprotective effects over the other three extracts and the drug reference standard. Conclusions: The findings revealed that Ambrette exerts promising protective effects against adriamycin-mediated acute kidney injury through antioxidant, anti-inflammatory, and anti-apoptosis pathways. A-HE might serve as a potential candidate for the development of therapeutic drug leads that will be beneficial in the treatment of acute kidney injury. en_US
dc.language.iso en en_US
dc.publisher Elsevier B.V. en_US
dc.subject Acute kidney injury en_US
dc.subject Ambrette en_US
dc.subject Anti-apoptosis effects en_US
dc.subject Anti-Inflammatory effects en_US
dc.subject Antioxidant potential en_US
dc.title Nephroprotective mechanisms of Ambrette (Abelmoschus moschatus Medik.) leaf extracts in adriamycin mediated acute kidney injury model of Wistar rats en_US
dc.type Article en_US


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