Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/11228
Title: Cytotoxic effects of α-Eleostearic acid-rich fat extracted from seeds of bitter melon (Momordica charantia) on Vero 76 cells
Authors: Ranasinghe, K.N.K.
Jayasooriya, A.P.
Premachandra, T.N.
Hilmi, A.J.
Kularatne, S.A.M.
Madhujith, T.
Rajapakse, R.P.V.J.
Keywords: Bitter melon
α - Eleostearic acid
Vero 76
Cytotoxicity
Issue Date: 2015
Publisher: Faculty of Graduate Studies, University of Kelaniya
Citation: Ranasinghe, K.N.K., Jayasooriya, A.P., Premachandra, T.N., Hilmi, A.J., Kularatne, S.A.M., Madhujith, T. and Rajapakse, R.P.V.J. 2015. Cytotoxic effects of α-Eleostearic acid-rich fat extracted from seeds of bitter melon (Momordica charantia) on Vero 76 cells, p. 177, In: Proceedings of the International Postgraduate Research Conference 2015 University of Kelaniya, Kelaniya, Sri Lanka, (Abstract), 339 pp.
Abstract: Some seed fat sources contain conjugated trienoic fatty acids in high proportions (30- 80%). Previous studies have revealed that these fatty acids possess potent anticarcinogenic properties. The bitter melon (Momordica charantia) seed fat contains a conjugated trieneoic fatty acid named α - Eleostearic acid (α – ESA; 18:3;9c,11t,13t). The reported proportion of α-ESA in the fatty acid profile ranges from 50% - 60% and it is consistent with our study giving a result of 50.56%. Thus, the current in vitro study was conducted to evaluate the cytotoxicity of α-ESA-rich fat using a continuous cell line named Vero 76. It has been previously suggested that Vero cells can be used for preliminary studies in cancer research in vitro. For the in vitro evaluation, fatty acid methyl esters (FAMEs) of bitter melon seed fat (BMO) was prepared and was incorporated into the cell line with RPMI 1640 medium (10μl FAME + 90μl RPMI medium). As a control, FAMEs of coconut fat (Cocos nucifera; CO) was incorporated (10μl FAME + 90μl RPMI medium) into growing cells. Furthermore, in the positive control, Absolute Ethanol (100 % Ethanol) was added (100μl) and in the negative control 100μl of RPMI medium was added. MTT assay was conducted after 24 hours incubation. Finally Absorbance (A) was measured at 570 nm. The results revealed that Vero cells treated with FAMEs of BMO have exhibited a significantly less cell viability (A = 0.2138) as compared with cells treated with FAMEs of CO (A = 0.8475). The viability of cells treated with FAMEs of CO was comparable with the negative control (A = 1.027). Interestingly, the viability of cells treated with FAMEs of BMO was comparable with the positive control (A = 0.2443) indicating a potent cytotoxicity on these cells. BMO exhibited a significant cytotoxic action compared with CO. As Vero cells have been recognized a suitable cell culture for preliminary cytotoxicity studies, these results pave the way for further studies on this cytotoxic conjugated fatty acid using cancer cell lines in vitro.
URI: http://repository.kln.ac.lk/handle/123456789/11228
Appears in Collections:IPRC - 2015

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