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ANTI-NUTRITIONAL CONSTITUENT OF COLOCASIA ESCULENTA ...

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C.1.2.3<br />

respoDSlble for transport of beta-sitosterol to other tissues in the body. Some beta­<br />

sitosterol is glueoronidated in the liver and a portion is also metabolized to cholic acid<br />

and chenodeoxycholic acid (Marteau et al., 1980). Excretion is mainly via the biliary<br />

route.<br />

In an attempt to improve sterol solubility, plant sterols have been esterified with fatty<br />

acids in order to prodoce oil-soluble plant sterol esters (Mattson, 1964, U.S. Patent No.<br />

5,502,045).<br />

Biological activities<br />

Beta-sitosterol offers a remarkable display ofscientifically recognized benefits for major<br />

areas ofhea1th. Health benefits include:<br />

• lowering cholesterol (Farquhar et al., 1956; Lees et ai, 1977);<br />

• anti-diabetic properties (Ivorra, 1988);<br />

• anti-tumor activities (Romero and Lichtenberger, 1990; Janezic and Rao, 1992);<br />

• anti-bacterial properties (Hess et al., 1995; Padmaja etaI., 1993);<br />

• anti-fungal abilities (Smania et al., 2003);<br />

• anti-inflammatory predilection (Bouic et al., 2001);<br />

• anti-atherogenecity activities (Moghadasian et aI., 1997);<br />

• anti-ulcer properties(Jayaraj et al., 2003); and<br />

• preventing cardiovascular events (Miettinen et al., 1990; Gylling and Miettinen,<br />

1997).<br />

Human research already includes the treatment ofhypercholesterolemia, benign prostatic<br />

hypertrophy (BPH) and rheumatoid arthritis with beta-sitosterol (pegel, 1997). Success in<br />

these areas, particularly with regard to cardiovascular diseases, may be attributed to the<br />

cholesterol-lowering effects ofplant sterols (Drexel et at., 1981; Miettinen et at., 2000).<br />

184

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