Cytotoxic effects of hydro-alcoholic extracts of cress (Lepidium Sativum) - made from different stages of the plant - on k۵۶۲ Leukemia cell line
Publish place: Hormozgan Medical Journal، Vol: 18، Issue: 5
Publish Year: 1393
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:
JR_HMJ-18-5_005
تاریخ نمایه سازی: 28 بهمن 1402
Abstract:
Introduction: Chronic myeloid leukemia (CML) is a malignant clonal disorder of hematopoietic stem cells resulting in the increase of myeloid cells, erythroid cells and platelets in the peripheral blood and hyperplasia in bone marrow. The research evaluated the cytotoxic effects of hydro-alcoholic extracts of Lepidium Sativum (Cress plant) shoots before and after flowering on K۵۶۲ cell line as a model of CML. Methods: In this laboratory experimental study, the Lepidium Sativum shoots including stems and leaves of the plant before flowering and its shoots after flowering including stems, leaves and flowers were collected from Afoos city (Iran). They were extracted using maceration (۵۰% Ethanol ۹۶% and ۵۰% water) method. K۵۶۲ cells were cultured. Then the cells were treated with different concentrations of the extract (۱۲.۵-۱۰۰ μg/ml) at different time intervals (۲۴, ۴۸ and ۷۲ hour). The Lepidium Sativum cytotoxicity was evaluated by the MTT test method before and after flowering against K۵۶۲ leukemia cells. The absorption was measured using an ELISA plate reader at ۵۴۰ nm wave length. Data were analyzed using SPSS۱۵ software and one-way ANOVA test analysis as well as Tukey test; where P<۰.۰۵ was considered significant. Results: Hydro-alcoholic extracts of Lepidium Sativum showed the most optimum cytotoxicity both before and after flowering with a dose of IC۵۰=۲۵ μg/ml and ۷۲ hour after treatment on K۵۶۲ cell line. In other words, hydro-alcoholic extracts of Lepidium Sativum prepared before and after flowering exhibited a dose and time dependent cytotoxic effect on K۵۶۲ cell line. Conclusion: Considering the cytotoxic effect of hydro-alcoholic extracts of Lepidium Sativum shoots before and after flowering on K۵۶۲ cells, the plant can be considered as a potential candidate for further studies on CML treatment.
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