Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon

In this study we investigated the chemopreventive effects of quercetin and rutin when added to standard AIN-76A diet and fed to normal and azoxymethane (AOM)-treated mice. Early changes in colonic mucosa were analyzed, including colonic cell proliferation, apoptotic cell death, cyclin D1 expression...

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Main Authors: YANG, K., Lamprecht, S. A., Liu, Y., Shinozaki, H., Fan, K. H., Leung, Denis H. Y., Newmark, H., Steele, V. E., Kelloff, G. J., Lipkin, M.
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Published: Institutional Knowledge at Singapore Management University 2000
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Online Access:https://ink.library.smu.edu.sg/soe_research/145
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spelling sg-smu-ink.soe_research-11442010-09-23T05:48:03Z Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon YANG, K. Lamprecht, S. A. Liu, Y. Shinozaki, H. Fan, K. H. Leung, Denis H. Y. Newmark, H. Steele, V. E. Kelloff, G. J. Lipkin, M. In this study we investigated the chemopreventive effects of quercetin and rutin when added to standard AIN-76A diet and fed to normal and azoxymethane (AOM)-treated mice. Early changes in colonic mucosa were analyzed, including colonic cell proliferation, apoptotic cell death, cyclin D1 expression and focal areas of dysplasia (FAD). The findings show that the number of colonic epithelial cells per crypt column increased (P < 0.01) in each normal mouse group fed the flavonoids; AOM administration increased colonic crypt cell proliferation and resulted in a marked rise of bromodeoxyuridine-labeled cells in the lower proliferative zone of the crypt. Both supplementary dietary quercetin and rutin increased the apoptotic index and caused a redistribution of apoptotic cells along the crypt axis in normal mice fed a standard AIN-76A diet. The number of apoptotic cells/column and apoptotic indices markedly increased (P < 0.01) in the AOM-treated group compared with untreated animals; apoptotic cells expanded throughout the colonic crypts after flavonoid supplementation and AOM administration. Positive cyclin D1 expression was detected in mice on diets supplemented either with quercetin (P < 0.01) or rutin (P < 0.05). AOM administration resulted in the formation of FAD. Both the number of mice exhibiting FAD and the total numer of FAD observed were significantly reduced (P < 0.01) in AOM-treated animals fed flavonoids compared with mice maintained on the standard AIN-76A diet. Surprisingly, however, quercetin alone was able to induce FAD in 22% of normal mice fed the standard AIN-76A diet. 2000-01-01T08:00:00Z text https://ink.library.smu.edu.sg/soe_research/145 info:doi/10.1093/carcin/21.9.1655 Research Collection School Of Economics eng Institutional Knowledge at Singapore Management University Econometrics Medicine and Health Sciences
institution Singapore Management University
building SMU Libraries
continent Asia
country Singapore
Singapore
content_provider SMU Libraries
collection InK@SMU
language English
topic Econometrics
Medicine and Health Sciences
spellingShingle Econometrics
Medicine and Health Sciences
YANG, K.
Lamprecht, S. A.
Liu, Y.
Shinozaki, H.
Fan, K. H.
Leung, Denis H. Y.
Newmark, H.
Steele, V. E.
Kelloff, G. J.
Lipkin, M.
Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon
description In this study we investigated the chemopreventive effects of quercetin and rutin when added to standard AIN-76A diet and fed to normal and azoxymethane (AOM)-treated mice. Early changes in colonic mucosa were analyzed, including colonic cell proliferation, apoptotic cell death, cyclin D1 expression and focal areas of dysplasia (FAD). The findings show that the number of colonic epithelial cells per crypt column increased (P < 0.01) in each normal mouse group fed the flavonoids; AOM administration increased colonic crypt cell proliferation and resulted in a marked rise of bromodeoxyuridine-labeled cells in the lower proliferative zone of the crypt. Both supplementary dietary quercetin and rutin increased the apoptotic index and caused a redistribution of apoptotic cells along the crypt axis in normal mice fed a standard AIN-76A diet. The number of apoptotic cells/column and apoptotic indices markedly increased (P < 0.01) in the AOM-treated group compared with untreated animals; apoptotic cells expanded throughout the colonic crypts after flavonoid supplementation and AOM administration. Positive cyclin D1 expression was detected in mice on diets supplemented either with quercetin (P < 0.01) or rutin (P < 0.05). AOM administration resulted in the formation of FAD. Both the number of mice exhibiting FAD and the total numer of FAD observed were significantly reduced (P < 0.01) in AOM-treated animals fed flavonoids compared with mice maintained on the standard AIN-76A diet. Surprisingly, however, quercetin alone was able to induce FAD in 22% of normal mice fed the standard AIN-76A diet.
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author YANG, K.
Lamprecht, S. A.
Liu, Y.
Shinozaki, H.
Fan, K. H.
Leung, Denis H. Y.
Newmark, H.
Steele, V. E.
Kelloff, G. J.
Lipkin, M.
author_facet YANG, K.
Lamprecht, S. A.
Liu, Y.
Shinozaki, H.
Fan, K. H.
Leung, Denis H. Y.
Newmark, H.
Steele, V. E.
Kelloff, G. J.
Lipkin, M.
author_sort YANG, K.
title Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon
title_short Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon
title_full Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon
title_fullStr Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon
title_full_unstemmed Chemoprevention Studies of the Flavonoids Quercetin and Rutin in Normal and Azoxymethane Treated Mouse Colon
title_sort chemoprevention studies of the flavonoids quercetin and rutin in normal and azoxymethane treated mouse colon
publisher Institutional Knowledge at Singapore Management University
publishDate 2000
url https://ink.library.smu.edu.sg/soe_research/145
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