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Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine

Five non‐genotoxic chemicals previously demonstrated to be bladder cancer promoters in 36‐week in vivo assays for carcinogenesis were reevaluated in a 20‐week experiment in order to assess the summation influence of dietary nracil, a component of RNA, on the development of (pre)neoplastic lesions. T...

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Autores principales: de Camargo, João Lauro Viana, Shirai, Tomoyuki, Kato, Toshio, Asamoto, Makoto, Shoji, Shoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918328/
https://www.ncbi.nlm.nih.gov/pubmed/1752781
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01784.x
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author de Camargo, João Lauro Viana
Shirai, Tomoyuki
Kato, Toshio
Asamoto, Makoto
Shoji, Shoji
author_facet de Camargo, João Lauro Viana
Shirai, Tomoyuki
Kato, Toshio
Asamoto, Makoto
Shoji, Shoji
author_sort de Camargo, João Lauro Viana
collection PubMed
description Five non‐genotoxic chemicals previously demonstrated to be bladder cancer promoters in 36‐week in vivo assays for carcinogenesis were reevaluated in a 20‐week experiment in order to assess the summation influence of dietary nracil, a component of RNA, on the development of (pre)neoplastic lesions. The test chemicals, sodium bicarbonate, sodium L‐ascorbate, sodium citrate, butylated hydroxytoluene and ethoxyquin, were mixed into the diet at concentrations of 3%, 5%, 5%, 1% and 0.8%, respectively, and administered to male F344 rats after initiation with 0,05% N‐butyl‐N‐(4‐hydroxybutyDnitrosamine (BBN) in their drinking water for 4 weeks. The test chemicals were given from the 4th to the 8th and the llth to 20th experimental weeks, uracil being administered at the level of 3% in the diet during the intervening period. Rats in the control group received only BBN and uracil. All animals were killed at week 20 and the bladders were evaluated for the occurrence of putative preneoplastic papillary or nodular (PN) hyperplasia and tumors. Significant increase in the occurrence of FN hyperplasia was observed in all groups initiated with BBN and fed uracil and test chemicals. Quantitative values for papillomas were also significantly increased except in the ethoxyquin‐treated group. The results confirm that uracil given in the middle of the post‐initiation stage enhances the promoting activity of chemicals and suggest that the use of this chemical might be useful to reduce the duration of current bioassays for bladder chemical carcinogens.
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spelling pubmed-59183282018-05-11 Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine de Camargo, João Lauro Viana Shirai, Tomoyuki Kato, Toshio Asamoto, Makoto Shoji, Shoji Jpn J Cancer Res Article Five non‐genotoxic chemicals previously demonstrated to be bladder cancer promoters in 36‐week in vivo assays for carcinogenesis were reevaluated in a 20‐week experiment in order to assess the summation influence of dietary nracil, a component of RNA, on the development of (pre)neoplastic lesions. The test chemicals, sodium bicarbonate, sodium L‐ascorbate, sodium citrate, butylated hydroxytoluene and ethoxyquin, were mixed into the diet at concentrations of 3%, 5%, 5%, 1% and 0.8%, respectively, and administered to male F344 rats after initiation with 0,05% N‐butyl‐N‐(4‐hydroxybutyDnitrosamine (BBN) in their drinking water for 4 weeks. The test chemicals were given from the 4th to the 8th and the llth to 20th experimental weeks, uracil being administered at the level of 3% in the diet during the intervening period. Rats in the control group received only BBN and uracil. All animals were killed at week 20 and the bladders were evaluated for the occurrence of putative preneoplastic papillary or nodular (PN) hyperplasia and tumors. Significant increase in the occurrence of FN hyperplasia was observed in all groups initiated with BBN and fed uracil and test chemicals. Quantitative values for papillomas were also significantly increased except in the ethoxyquin‐treated group. The results confirm that uracil given in the middle of the post‐initiation stage enhances the promoting activity of chemicals and suggest that the use of this chemical might be useful to reduce the duration of current bioassays for bladder chemical carcinogens. Blackwell Publishing Ltd 1991-11 /pmc/articles/PMC5918328/ /pubmed/1752781 http://dx.doi.org/10.1111/j.1349-7006.1991.tb01784.x Text en
spellingShingle Article
de Camargo, João Lauro Viana
Shirai, Tomoyuki
Kato, Toshio
Asamoto, Makoto
Shoji, Shoji
Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine
title Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine
title_full Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine
title_fullStr Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine
title_full_unstemmed Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine
title_short Summation Effects of Uracil and Other Promoters on Epithelial Lesion Development in the F344 Rat Urinary Bladder Initiated by N‐Butyl‐N‐(4‐hydroxybutyl)nitrosamine
title_sort summation effects of uracil and other promoters on epithelial lesion development in the f344 rat urinary bladder initiated by n‐butyl‐n‐(4‐hydroxybutyl)nitrosamine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918328/
https://www.ncbi.nlm.nih.gov/pubmed/1752781
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01784.x
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