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Determination of in vitro antioxidant activity and in vivo antineoplastic effects against Ehrlich ascites carcinoma of methanolic extract of Sphagneticola calendulacea (L.) Pruski

BACKGROUND AND AIM: Sphagneticola calendulacea (L.) Pruski (S. calendulacea) is a well-known medicinal plant that is widely used in traditional medicine. This study was conducted to evaluate the antioxidant and antineoplastic properties of S. calendulacea leaf. EXPERIMENTAL PROCEDURE: Methanol was u...

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Detalles Bibliográficos
Autores principales: Bari, Md. Wasim, Islam, Ariful, Islam, Md. Monirul, Sultana, Mst Julia, Afroz, Rashida, Khan, Md. Mahbubur Rahman, Parul, Salina Shaheen, Swaraz, A.M., Hossain, Mohammad Ismail, Islam, Mohammad Amirul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215174/
https://www.ncbi.nlm.nih.gov/pubmed/34189294
http://dx.doi.org/10.1016/j.heliyon.2021.e07228
Descripción
Sumario:BACKGROUND AND AIM: Sphagneticola calendulacea (L.) Pruski (S. calendulacea) is a well-known medicinal plant that is widely used in traditional medicine. This study was conducted to evaluate the antioxidant and antineoplastic properties of S. calendulacea leaf. EXPERIMENTAL PROCEDURE: Methanol was used as a solvent to prepare leaf extract from the dried leaf of S. calendulacea (MESL). We have evaluated the total phenolic and flavonoid contents of MESL, and using five different assays; we have also evaluated the antioxidant property of MESL. In vivo antineoplastic activity of MESL against Ehrlich ascites carcinoma (EAC) cells in experimental mice was also explored. RESULTS: The phytochemical analysis of MESL exhibited the total phenolic, and total flavonoid contents in the dry extracts were 32.86 mg/gm of gallic acid equivalent and 127.26 mg/gm of catechin equivalent, respectively. Moreover, MESL also showed promising scavenging activity in all assays (IC(50) value ≥70.5 μg/mL). In the in vivo antineoplastic assay, MESL showed increased EAC cell death at the doses of 50 mg/kg and 100 mg/kg body weight. MESL administration also induced apoptosis of EAC cells, significantly inhibited EAC cell growth, and increased the life span of EAC cell-bearing mice compared to EAC cell-bearing control mice. CONCLUSIONS: All findings of this study suggest potential antioxidant and antineoplastic properties of MESL.