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Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats

The inhibitory effect of dietary perilla oil rich in the n‐3 polyunsaturated fatty acid α‐linolenic acid against colon carcinogenesis was investigated in rats. Four groups of 26 F344 rats each received an intrarectal dose of 2 mg of N‐methyl‐N‐nitrosourea 3 times a week for 2 weeks, and received a d...

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Autores principales: Narisawa, Tomio, Takahashi, Masahiro, Kotanagi, Hitoshi, Kusaka, Hisashi, Yamazaki, Yoshihiko, Koyama, Hirofumi, Fukaura, Yoko, Nishizawa, Yukio, Kotsugai, Mieko, Isoda, Yoshihiro, Hirano, Jiro, Noritoshi, Noritoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918260/
https://www.ncbi.nlm.nih.gov/pubmed/1683347
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01762.x
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author Narisawa, Tomio
Takahashi, Masahiro
Kotanagi, Hitoshi
Kusaka, Hisashi
Yamazaki, Yoshihiko
Koyama, Hirofumi
Fukaura, Yoko
Nishizawa, Yukio
Kotsugai, Mieko
Isoda, Yoshihiro
Hirano, Jiro
Noritoshi, Noritoshi
author_facet Narisawa, Tomio
Takahashi, Masahiro
Kotanagi, Hitoshi
Kusaka, Hisashi
Yamazaki, Yoshihiko
Koyama, Hirofumi
Fukaura, Yoko
Nishizawa, Yukio
Kotsugai, Mieko
Isoda, Yoshihiro
Hirano, Jiro
Noritoshi, Noritoshi
author_sort Narisawa, Tomio
collection PubMed
description The inhibitory effect of dietary perilla oil rich in the n‐3 polyunsaturated fatty acid α‐linolenic acid against colon carcinogenesis was investigated in rats. Four groups of 26 F344 rats each received an intrarectal dose of 2 mg of N‐methyl‐N‐nitrosourea 3 times a week for 2 weeks, and received a diet containing 12% perilla oil, 6% or 12% safflower oil (rich in the n‐6 polyunsaturated fatty acid linoleic acid), or 12% palm oil (rich in saturated and monounsaturated fatty acids). At week 35, the incidence of colon cancer was significantly lower in perilla oil‐fed rats than in other dietary groups; 19% vs. 46%, 56% and 58%. When examined at week 10, the concentration of fecal bile acids, known to be tumor promoters, was not significantly different among the dietary groups, and the intrarectal deoxycholic acid‐induced colonic mucosal ornithine decarboxylase activity, a marker of tumor promotion, was significantly lower in perilla oil‐fed group than in other groups. The serum and colonic mucosal fatty acid compositions and the blood plasma prostaglandin E(2) level directly reflected the fatty acid composition of each dietary fat. The results suggest that the anti‐tumor‐promoting effect of dietary perilla oil was a result of a decreased sensitivity of colonic mucosa to tumor promoters arising from the altered fatty acid composition in membrane phospholipid of colonic epithelial cells, and was not a consequence of a decrease of promoters such as bile acids.
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spelling pubmed-59182602018-05-11 Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats Narisawa, Tomio Takahashi, Masahiro Kotanagi, Hitoshi Kusaka, Hisashi Yamazaki, Yoshihiko Koyama, Hirofumi Fukaura, Yoko Nishizawa, Yukio Kotsugai, Mieko Isoda, Yoshihiro Hirano, Jiro Noritoshi, Noritoshi Jpn J Cancer Res Article The inhibitory effect of dietary perilla oil rich in the n‐3 polyunsaturated fatty acid α‐linolenic acid against colon carcinogenesis was investigated in rats. Four groups of 26 F344 rats each received an intrarectal dose of 2 mg of N‐methyl‐N‐nitrosourea 3 times a week for 2 weeks, and received a diet containing 12% perilla oil, 6% or 12% safflower oil (rich in the n‐6 polyunsaturated fatty acid linoleic acid), or 12% palm oil (rich in saturated and monounsaturated fatty acids). At week 35, the incidence of colon cancer was significantly lower in perilla oil‐fed rats than in other dietary groups; 19% vs. 46%, 56% and 58%. When examined at week 10, the concentration of fecal bile acids, known to be tumor promoters, was not significantly different among the dietary groups, and the intrarectal deoxycholic acid‐induced colonic mucosal ornithine decarboxylase activity, a marker of tumor promotion, was significantly lower in perilla oil‐fed group than in other groups. The serum and colonic mucosal fatty acid compositions and the blood plasma prostaglandin E(2) level directly reflected the fatty acid composition of each dietary fat. The results suggest that the anti‐tumor‐promoting effect of dietary perilla oil was a result of a decreased sensitivity of colonic mucosa to tumor promoters arising from the altered fatty acid composition in membrane phospholipid of colonic epithelial cells, and was not a consequence of a decrease of promoters such as bile acids. Blackwell Publishing Ltd 1991-10 /pmc/articles/PMC5918260/ /pubmed/1683347 http://dx.doi.org/10.1111/j.1349-7006.1991.tb01762.x Text en
spellingShingle Article
Narisawa, Tomio
Takahashi, Masahiro
Kotanagi, Hitoshi
Kusaka, Hisashi
Yamazaki, Yoshihiko
Koyama, Hirofumi
Fukaura, Yoko
Nishizawa, Yukio
Kotsugai, Mieko
Isoda, Yoshihiro
Hirano, Jiro
Noritoshi, Noritoshi
Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats
title Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats
title_full Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats
title_fullStr Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats
title_full_unstemmed Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats
title_short Inhibitory Effect of Dietary Perilla Oil Rich in the n‐3 Polyunsaturated Fatty Acid α‐Linolenic Acid on Colon Carcinogenesis in Rats
title_sort inhibitory effect of dietary perilla oil rich in the n‐3 polyunsaturated fatty acid α‐linolenic acid on colon carcinogenesis in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918260/
https://www.ncbi.nlm.nih.gov/pubmed/1683347
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01762.x
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