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ANTI-NUTRITIONAL CONSTITUENT OF COLOCASIA ESCULENTA ...

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C.4.1 Introduction<br />

CHAPTERC-4<br />

DISCUSSION<br />

This section ofthe study was conducted to investigate the effects ofbeta-sitosterol on the<br />

digestive and absorptive enzymes of Sprague-Dawley rats. Results obtained for the<br />

nutritional evaluation are discussed in this chapter.<br />

C.4.2 Experimental test<br />

The rats were in good health throughout the study: no mortality was observed in any of<br />

the groups tested with beta-sitosterol. This is in agreement with studies conducted on<br />

phytosterols. Similar studies have consistently demonstrated a lack oftoxicity in animals<br />

and humans fed beta-sitosterol., except for individuals with an extremely rare genetic<br />

condition, sitostero1aemia (Malini and Vanithakumari, 1990; Hicks and Morean, 2001).<br />

Plasma phytosterol levels are generally very low in mammalian tissues. Poor absorption<br />

from the intestine and quicker excretion from the liver, compared to that of cholesterol,<br />

are responsible for these low levels (Ling and Jones, 1995). Intestinal absorption of total<br />

dietary beta-sitosterol consumed is negligible in mammals. Animal studies have<br />

demonstrated that this absorption should possibly be as little as five percent (Borgstrom,<br />

1968; Gould, 1955). In rats, the absorption of beta-sitosterol is about four percent<br />

(Sanders et al., 2000). A reason for the low absorption ofplant sterols might be that plant<br />

sterols are poorly esterified, possibly due to the low affinity ofACAT (acyl-coenzyme A<br />

cholesterol acyltransferase) for these components (Bhattacharyya, 1981; Ntauios et al.,<br />

1998). Within the enterocyte, free cholesterol is is esterified by ACAT, incorporated into<br />

chylomicrons, which are subsequently excreted into the circulation and converted into a<br />

chylomicron-remnant by the action oflipoprotein lipase (Kwiterovich, 2000). Absorption<br />

212

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