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Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity

Four organosulfur compounds from garlic and onions were examined for modifying effects on diethylnitrosamine (DEN)‐induced neoplasia of the liver in male F344 rats using the medium‐term bioassay system based on the two‐step model of hepatocarcinogenesis. Carcinogenic potential was scored by comparin...

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Detalles Bibliográficos
Autores principales: Takada, Nobuyasu, Kitano, Mitsuaki, Chen, Tianxin, Yano, Yoshihisa, Otani, Shuzo, Fukushima, Shoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919373/
https://www.ncbi.nlm.nih.gov/pubmed/7829389
http://dx.doi.org/10.1111/j.1349-7006.1994.tb02908.x
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author Takada, Nobuyasu
Kitano, Mitsuaki
Chen, Tianxin
Yano, Yoshihisa
Otani, Shuzo
Fukushima, Shoji
author_facet Takada, Nobuyasu
Kitano, Mitsuaki
Chen, Tianxin
Yano, Yoshihisa
Otani, Shuzo
Fukushima, Shoji
author_sort Takada, Nobuyasu
collection PubMed
description Four organosulfur compounds from garlic and onions were examined for modifying effects on diethylnitrosamine (DEN)‐induced neoplasia of the liver in male F344 rats using the medium‐term bioassay system based on the two‐step model of hepatocarcinogenesis. Carcinogenic potential was scored by comparing the numbers and areas per cm(2) of induced glutathlone S‐transfcrasc placental form‐positive foci. Isothiocyanic acid isobutyl ester (IAIE), dipropyl trisulfide (DPT), and allyl mercapton (AM) exerted enhancing effects on their development, while dimethyl trisulfide also tended to increase them. To investigate possible mechanisms of the modifying influence, sequential changes in ornithine decarboxylase activity (ODC) over 24 h were measured in AM‐treated liver tissue without prior DEN initiation. The activity started to increase by 4 h after AM‐treatment, and reached maximum at 16 h, compared to controls. Spermidine/spermine N(1)‐acetyltransferase activity was not significantly changed. An increase in proliferating cell nuclear antigen‐positive cells followed the elevation of ODC activity. These results suggest that IAIE, DPT, and AM promote rat hepatocarcinogenesis and their promoting effect might be caused by increased cell proliferation with increased poly‐amine biosynthesis. In evaluating relationships between diet and cancer, it is thus appropriate to consider not only a possible protective role of garlic and onions, but also enhancing effects.
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spelling pubmed-59193732018-05-11 Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity Takada, Nobuyasu Kitano, Mitsuaki Chen, Tianxin Yano, Yoshihisa Otani, Shuzo Fukushima, Shoji Jpn J Cancer Res Article Four organosulfur compounds from garlic and onions were examined for modifying effects on diethylnitrosamine (DEN)‐induced neoplasia of the liver in male F344 rats using the medium‐term bioassay system based on the two‐step model of hepatocarcinogenesis. Carcinogenic potential was scored by comparing the numbers and areas per cm(2) of induced glutathlone S‐transfcrasc placental form‐positive foci. Isothiocyanic acid isobutyl ester (IAIE), dipropyl trisulfide (DPT), and allyl mercapton (AM) exerted enhancing effects on their development, while dimethyl trisulfide also tended to increase them. To investigate possible mechanisms of the modifying influence, sequential changes in ornithine decarboxylase activity (ODC) over 24 h were measured in AM‐treated liver tissue without prior DEN initiation. The activity started to increase by 4 h after AM‐treatment, and reached maximum at 16 h, compared to controls. Spermidine/spermine N(1)‐acetyltransferase activity was not significantly changed. An increase in proliferating cell nuclear antigen‐positive cells followed the elevation of ODC activity. These results suggest that IAIE, DPT, and AM promote rat hepatocarcinogenesis and their promoting effect might be caused by increased cell proliferation with increased poly‐amine biosynthesis. In evaluating relationships between diet and cancer, it is thus appropriate to consider not only a possible protective role of garlic and onions, but also enhancing effects. Blackwell Publishing Ltd 1994-11 /pmc/articles/PMC5919373/ /pubmed/7829389 http://dx.doi.org/10.1111/j.1349-7006.1994.tb02908.x Text en
spellingShingle Article
Takada, Nobuyasu
Kitano, Mitsuaki
Chen, Tianxin
Yano, Yoshihisa
Otani, Shuzo
Fukushima, Shoji
Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity
title Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity
title_full Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity
title_fullStr Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity
title_full_unstemmed Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity
title_short Enhancing Effects of Organosulfur Compounds from Garlic and Onions on Hepatocarcinogenesis in Rats: Association with Increased Cell Proliferation and Elevated Ornithine Decarboxylase Activity
title_sort enhancing effects of organosulfur compounds from garlic and onions on hepatocarcinogenesis in rats: association with increased cell proliferation and elevated ornithine decarboxylase activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919373/
https://www.ncbi.nlm.nih.gov/pubmed/7829389
http://dx.doi.org/10.1111/j.1349-7006.1994.tb02908.x
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