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Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats

β‐Cryptoxanthin (βCx), one of 4 major carotenoids in the blood, was investigated for anticarcinogenic activity in F344 rats. Four groups of 25 rats each received an intrarectal dose of 2 mg of N‐methylnitrosourea 3 times a week for 5 weeks, and were fed the diet supplemented with 0 ppm (control), 25...

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Detalles Bibliográficos
Autores principales: Narisawa, Tomio, Fukaura, Yoko, Oshima, Shunji, Inakuma, Takahiro, Yano, Masamichi, Nishino, Hoyoku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5925991/
https://www.ncbi.nlm.nih.gov/pubmed/10595732
http://dx.doi.org/10.1111/j.1349-7006.1999.tb00677.x
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author Narisawa, Tomio
Fukaura, Yoko
Oshima, Shunji
Inakuma, Takahiro
Yano, Masamichi
Nishino, Hoyoku
author_facet Narisawa, Tomio
Fukaura, Yoko
Oshima, Shunji
Inakuma, Takahiro
Yano, Masamichi
Nishino, Hoyoku
author_sort Narisawa, Tomio
collection PubMed
description β‐Cryptoxanthin (βCx), one of 4 major carotenoids in the blood, was investigated for anticarcinogenic activity in F344 rats. Four groups of 25 rats each received an intrarectal dose of 2 mg of N‐methylnitrosourea 3 times a week for 5 weeks, and were fed the diet supplemented with 0 ppm (control), 25 ppm, 5 ppm or 1 ppm βCx throughout the experiment. The colon cancer incidence at week 30 was significantly lower in the βCx (25 ppm) diet group, but not in the βCx (5 ppm) and βCx (1 ppm) diet groups, than in the control diet group: 68%, 84%, 80% vs. 96%. The results suggested that dietary βCx may affect colon carcinogenesis after accumulation in the colonic mucosa, perhaps due to absorption from the colon as well as the small intestine.
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spelling pubmed-59259912018-05-11 Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats Narisawa, Tomio Fukaura, Yoko Oshima, Shunji Inakuma, Takahiro Yano, Masamichi Nishino, Hoyoku Jpn J Cancer Res Article β‐Cryptoxanthin (βCx), one of 4 major carotenoids in the blood, was investigated for anticarcinogenic activity in F344 rats. Four groups of 25 rats each received an intrarectal dose of 2 mg of N‐methylnitrosourea 3 times a week for 5 weeks, and were fed the diet supplemented with 0 ppm (control), 25 ppm, 5 ppm or 1 ppm βCx throughout the experiment. The colon cancer incidence at week 30 was significantly lower in the βCx (25 ppm) diet group, but not in the βCx (5 ppm) and βCx (1 ppm) diet groups, than in the control diet group: 68%, 84%, 80% vs. 96%. The results suggested that dietary βCx may affect colon carcinogenesis after accumulation in the colonic mucosa, perhaps due to absorption from the colon as well as the small intestine. Blackwell Publishing Ltd 1999-10 /pmc/articles/PMC5925991/ /pubmed/10595732 http://dx.doi.org/10.1111/j.1349-7006.1999.tb00677.x Text en
spellingShingle Article
Narisawa, Tomio
Fukaura, Yoko
Oshima, Shunji
Inakuma, Takahiro
Yano, Masamichi
Nishino, Hoyoku
Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats
title Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats
title_full Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats
title_fullStr Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats
title_full_unstemmed Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats
title_short Chemoprevention by the Oxygenated Carotenoid β‐Cryptoxanthin of N‐Methylnitrosourea‐induced Colon Carcinogenesis in F344 Rats
title_sort chemoprevention by the oxygenated carotenoid β‐cryptoxanthin of n‐methylnitrosourea‐induced colon carcinogenesis in f344 rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5925991/
https://www.ncbi.nlm.nih.gov/pubmed/10595732
http://dx.doi.org/10.1111/j.1349-7006.1999.tb00677.x
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