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Investigation on the Antioxidant Activity of Roots and Stem of Colchicum turcicum L.
Corresponding Author(s) : Yesim Yesiloglu
Asian Journal of Chemistry,
Vol. 26 No. 1 (2014): Vol 26 Issue 1
Abstract
Water and acetone extracts from Colchicum turcicum L. were investigated for their antioxidant and radical scavenging activities in four different assays, namely, total antioxidant activity, 1,1-dipenyl-2-picryl-hydrazyl (DPPH) free radical scavenging, hydrogen peroxide scavenging and ferrous chelating activities. Antioxidant activity, ferrous chelating and hydrogen peroxide scavenging activities of C. turcicum extracts showed dose dependence and increased with concentration of C. turcicum extract. At the same concentration (100 μg/mL), water extract of C. turcicum (WECT) and acetone extract of C. turcicum (AECT) showed 53 and 48 % inhibition of lipid peroxidation of linoleic acid emulsion, respectively. On the other hand, butylated hydroxyanisole, butylated hydroxytoluene and ascorbic acid indicated inhibitions of 77, 71 and 59 % on the peroxidation of linoleic acid emulsion, respectively, at 50 μg/mL. Also, the total phenolic content in both water extract of C. turcicum and acetone extract of C. turcicum were determined as catechol equivalents. The total phenolics content of water and acetone extracts were determined by the Folin-Ciocalteu procedure and 0.454 and 2.172 mg catechol equivalent of phenols was detected in 1 g water extract of C. turcicum and acetone extract of C. turcicum.
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References
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R.S. Farag, A.Z.M.A. Badei, F.M. Hewedi and G.S.A. El-Baroty, J. Am. Oil Chem. Soc., 66, 792 (1989); doi:10.1007/BF02653670.
Y. Yeşiloğlu and L. Şit, Spectrochim. Acta [A], 95, 100 (2012); doi:10.1016/j.saa.2012.04.036.
Y.Yesiloglu, H. Aydin and I. Kilic, Asian J. Chem., 25, in press.
B. Nordenstam, “Colchicaceae”, In: Kubitzki, K. (Ed.), “The Families and General of Vascular Plants”, “Part III Flowering Plants”, “Monocotyledons”, “Lilianae” (except Orchidaceae). SpringerVerlag, Berlin, Heidelberg, New York, 175, (1998).
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R.A. Terkeltaub, N. Engl. J. Med., 349, 1647 (2003); doi:10.1056/NEJMcp030733.
J.P. Drenth and J.W. Van Der Meer, N. Engl. J. Med., 345, 1748 (2001); doi:10.1056/NEJMra010200.
T. Sakane and M. Takeno, Expert Opin. Investig. Drugs, 9, 1993 (2000); doi:10.1517/13543784.9.9.1993.
O.J. Eigsti and J.P. Dustin, “Colchicine in agriculture, medicine, biology, and chemistry”, The Iowa State College Press, Ames, 255 (1955).
F.Q. Alali, K. Tawaha and T. El-Elimat, Pharmazie, 62, 739 (2007).
N.E. Basova, E.V. Rozengart and A.A. Suvorov, Dokl. Biochem. Biophys., 406, 27 (2006); doi:10.1134/S160767290601008X.
K. Slinkard and V.L. Singleton, Am. J. Enol. Vitic., 28, 49 (1977).
D. Kim, S. Jeong and C.H. Lee, Food Chem., 81, 321 (2003); doi:10.1016/S0308-8146(02)00423-5.
J. Wang, X. Yuan, Z. Jin, Y. Tian and H. Song, Food Chem., 104, 242 (2007); doi:10.1016/j.foodchem.2006.11.035.
M.S. Blois, Nature, 181, 1199 (1958); doi:10.1038/1811199a0.
İ. Gülçin, Life Sci., 78, 803 (2006); doi:10.1016/j.lfs.2005.05.103.
R.J. Ruch, S.J. Cheng and J.E. Klaunig, Carcinogenesis, 10, 1003 (1989); doi:10.1093/carcin/10.6.1003.
K. Dastmalchi, H.J. Damien Dorman, P.P. Oinonen, Y. Darwis, I. Laakso and R. Hiltunen, LWT- Food Sci. Technol, 41, 391 (2008); doi:10.1016/j.lwt.2007.03.007.
Y. Pan, K. Wang, S. Huang, H. Wang, X. Mu, C. He, X. Ji, J. Zhang and F. Huang, Food Chem., 106, 1264 (2008); doi:10.1016/j.foodchem.2007.07.033.
A. Ardestani and R. Yazdanparast, Food Chem., 104, 21 (2007); doi:10.1016/j.foodchem.2006.10.066.
A. Meda, C.E. Lamien, M. Romito, J. Millogo and O.G. Nacoulma, Food Chem., 91, 571 (2005); doi:10.1016/j.foodchem.2004.10.006.
G. Miliauskas, P.R. Venskutonis and T.A. Van Beek, Food Chem., 85, 231 (2004); doi:10.1016/j.foodchem.2003.05.007.
B. Halliwell and J.M.C. Gutteridge, Biochem. J., 219, 1 (1984).