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Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats

This study was conducted to determine the concordance of results for a pair of structural isomers, 2-nitropropane (2-NP) and 1-nitropropane (1-NP), using the rat medium-term liver carcinogenesis bioassay (Ito test) and previously published long-term carcinogenicity tests. Male F344 rats were given a...

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Autores principales: Doi, Yuko, Tamano, Seiko, Kawabe, Mayumi, Sano, Masashi, Imai, Norio, Nakashima, Hironao, Furukawa, Fumio, Hagiwara, Akihiro, Otsuka, Masanori, Shirai, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Toxicologic Pathology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266355/
https://www.ncbi.nlm.nih.gov/pubmed/22319232
http://dx.doi.org/10.1293/tox.24.207
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author Doi, Yuko
Tamano, Seiko
Kawabe, Mayumi
Sano, Masashi
Imai, Norio
Nakashima, Hironao
Furukawa, Fumio
Hagiwara, Akihiro
Otsuka, Masanori
Shirai, Tomoyuki
author_facet Doi, Yuko
Tamano, Seiko
Kawabe, Mayumi
Sano, Masashi
Imai, Norio
Nakashima, Hironao
Furukawa, Fumio
Hagiwara, Akihiro
Otsuka, Masanori
Shirai, Tomoyuki
author_sort Doi, Yuko
collection PubMed
description This study was conducted to determine the concordance of results for a pair of structural isomers, 2-nitropropane (2-NP) and 1-nitropropane (1-NP), using the rat medium-term liver carcinogenesis bioassay (Ito test) and previously published long-term carcinogenicity tests. Male F344 rats were given a single intraperitoneal injection of DEN (200 mg/kg b.w.) to initiate hepatocarcinogenesis. After 2 weeks, they received per os 0, 0.8, 4 or 20 mg/kg/day of 2-NP or 1-NP six times a week and were subjected to two-thirds partial hepatectomy at week 3. Non-initiated groups receiving 0 or 20 mg/kg/day were also included. The animals were sacrificed for quantitative analysis of GST-P-positive foci at week 8. With the highest dose of 2-NP, significantly increased numbers and areas of GST-P-positive foci were demonstrated as compared with the respective control but were not noted with 1-NP. In the non-DEN-initiated groups, many small GST-P-positive foci of less than 0.2 mm in diameter were also induced in the rats treated with 2-NP at 20 mg/kg/day but were lacking with 1-NP. These results strongly support that 2-NP is a complete hepatocarcinogen with a potent initiation activity, whereas 1-NP is not.
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spelling pubmed-32663552012-02-08 Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats Doi, Yuko Tamano, Seiko Kawabe, Mayumi Sano, Masashi Imai, Norio Nakashima, Hironao Furukawa, Fumio Hagiwara, Akihiro Otsuka, Masanori Shirai, Tomoyuki J Toxicol Pathol Original This study was conducted to determine the concordance of results for a pair of structural isomers, 2-nitropropane (2-NP) and 1-nitropropane (1-NP), using the rat medium-term liver carcinogenesis bioassay (Ito test) and previously published long-term carcinogenicity tests. Male F344 rats were given a single intraperitoneal injection of DEN (200 mg/kg b.w.) to initiate hepatocarcinogenesis. After 2 weeks, they received per os 0, 0.8, 4 or 20 mg/kg/day of 2-NP or 1-NP six times a week and were subjected to two-thirds partial hepatectomy at week 3. Non-initiated groups receiving 0 or 20 mg/kg/day were also included. The animals were sacrificed for quantitative analysis of GST-P-positive foci at week 8. With the highest dose of 2-NP, significantly increased numbers and areas of GST-P-positive foci were demonstrated as compared with the respective control but were not noted with 1-NP. In the non-DEN-initiated groups, many small GST-P-positive foci of less than 0.2 mm in diameter were also induced in the rats treated with 2-NP at 20 mg/kg/day but were lacking with 1-NP. These results strongly support that 2-NP is a complete hepatocarcinogen with a potent initiation activity, whereas 1-NP is not. The Japanese Society of Toxicologic Pathology 2011-12 2012-01-07 /pmc/articles/PMC3266355/ /pubmed/22319232 http://dx.doi.org/10.1293/tox.24.207 Text en ©2011 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original
Doi, Yuko
Tamano, Seiko
Kawabe, Mayumi
Sano, Masashi
Imai, Norio
Nakashima, Hironao
Furukawa, Fumio
Hagiwara, Akihiro
Otsuka, Masanori
Shirai, Tomoyuki
Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats
title Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats
title_full Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats
title_fullStr Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats
title_full_unstemmed Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats
title_short Concordance between Results of Medium-term Liver Carcinogenesis Bioassays and Long-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane in F344 Rats
title_sort concordance between results of medium-term liver carcinogenesis bioassays and long-term findings for carcinogenic 2-nitropropane and non-carcinogenic 1-nitropropane in f344 rats
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266355/
https://www.ncbi.nlm.nih.gov/pubmed/22319232
http://dx.doi.org/10.1293/tox.24.207
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