Jh. Exon et al., DIETARY QUERCETIN, IMMUNE FUNCTIONS AND COLONIC CARCINOGENESIS IN RATS, Immunopharmacology and immunotoxicology, 20(1), 1998, pp. 173-190
Rats fed 100 mg/kg quercetin (QUE) daily for 7 weeks had significantly
enhanced natural killer cell activity compared to their vehicle (VEH)
-fed control. In contrast, rats fed 100 mg/kg QUE and treated with the
colon carcinogen, azoxymethane had significantly reduced natural kill
er cell activity compared to their VEH-fed azoxymethane-treated contro
l. There was no significant difference in natural killer cell activity
between the two control groups. Antibody production and delayed-type
hypersensitivity were not altered by QUE feeding in any treatment grou
p. In vitro exposure of splenic natural killer cells to 1mM QUE signif
icantly decreased natural killer cell cytotoxicity. Lower QUE concentr
ations produced a non-significant reduction in natural killer cell act
ivity that was restored to control values at 1x10(-13)M QUE. The distr
ibution, multiplicity and total number of colonic preneoplastic lesion
s, aberrant crypt foci, was not significantly different in the QUE-fed
azoxymethane-treated rats when compared to azoxymethane-treated vehic
le-fed rats at the conclusion of the 7 week feeding period. We found n
o correlation between immune function and development of preneoplastic
colon lesions in this study.