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No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats

To clarify the modifying effect of N-Acetyl-L-Cysteine (NAC), which has antioxidative ability, on hepatocarcinogenesis promoted by fenofibrate (FF), a peroxisome proliferator-activated receptor (PPAR) alpha agonist , male F344/N rats were administered a single intraperitoneal injection of N-diethyln...

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Autores principales: Nishimura, Jihei, Dewa, Yasuaki, Jin, Meilan, Saegusa, Yukie, Kawai, Masaomi, Kemmochi, Sayaka, Shimamoto, Keisuke, Harada, Tomoaki, Itoh, Tadashi, Shima, Tomomi, Shibutani, Makoto, Mitsumori, Kunitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Toxicologic Pathology 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234604/
https://www.ncbi.nlm.nih.gov/pubmed/22272000
http://dx.doi.org/10.1293/tox.22.255
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author Nishimura, Jihei
Dewa, Yasuaki
Jin, Meilan
Saegusa, Yukie
Kawai, Masaomi
Kemmochi, Sayaka
Shimamoto, Keisuke
Harada, Tomoaki
Itoh, Tadashi
Shima, Tomomi
Shibutani, Makoto
Mitsumori, Kunitoshi
author_facet Nishimura, Jihei
Dewa, Yasuaki
Jin, Meilan
Saegusa, Yukie
Kawai, Masaomi
Kemmochi, Sayaka
Shimamoto, Keisuke
Harada, Tomoaki
Itoh, Tadashi
Shima, Tomomi
Shibutani, Makoto
Mitsumori, Kunitoshi
author_sort Nishimura, Jihei
collection PubMed
description To clarify the modifying effect of N-Acetyl-L-Cysteine (NAC), which has antioxidative ability, on hepatocarcinogenesis promoted by fenofibrate (FF), a peroxisome proliferator-activated receptor (PPAR) alpha agonist , male F344/N rats were administered a single intraperitoneal injection of N-diethylnitrosamine (DEN) as an initiator followed by administration of a diet containing 3,000 ppm of FF for 16 weeks. Two-thirds partial hepatectomy was performed 1 week after the FF treatment. Additionally, NAC treatments for 14 weeks from 2 weeks after the FF treatment were performed. Although the expression level of tumor protein p53 (Tp53) mRNA decreased in the DEN+FF+NAC group as compared with that in the DEN+FF group, no significant differences between the DEN+FF and DEN+FF+NAC groups were observed in the number of hepatocellular altered foci and activities of hepatocellular proliferation. In addition, the results of an antioxidant enzyme assay and measurement of the amounts of total glutathione in the liver revealed no significant difference between the DEN+FF and DEN+FF+NAC groups; although no significant differences were observed in many genes between the DEN+FF and DEN+FF+NAC groups, only glutathione peroxidase 2 (Gpx2) mRNA increased in the DEN+FF+NAC group as compared with the DEN+FF group. The results under the present experimental conditions indicate no obvious modifying effect of NAC on liver tumor promotion by FF in rats.
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spelling pubmed-32346042012-01-23 No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats Nishimura, Jihei Dewa, Yasuaki Jin, Meilan Saegusa, Yukie Kawai, Masaomi Kemmochi, Sayaka Shimamoto, Keisuke Harada, Tomoaki Itoh, Tadashi Shima, Tomomi Shibutani, Makoto Mitsumori, Kunitoshi J Toxicol Pathol Original To clarify the modifying effect of N-Acetyl-L-Cysteine (NAC), which has antioxidative ability, on hepatocarcinogenesis promoted by fenofibrate (FF), a peroxisome proliferator-activated receptor (PPAR) alpha agonist , male F344/N rats were administered a single intraperitoneal injection of N-diethylnitrosamine (DEN) as an initiator followed by administration of a diet containing 3,000 ppm of FF for 16 weeks. Two-thirds partial hepatectomy was performed 1 week after the FF treatment. Additionally, NAC treatments for 14 weeks from 2 weeks after the FF treatment were performed. Although the expression level of tumor protein p53 (Tp53) mRNA decreased in the DEN+FF+NAC group as compared with that in the DEN+FF group, no significant differences between the DEN+FF and DEN+FF+NAC groups were observed in the number of hepatocellular altered foci and activities of hepatocellular proliferation. In addition, the results of an antioxidant enzyme assay and measurement of the amounts of total glutathione in the liver revealed no significant difference between the DEN+FF and DEN+FF+NAC groups; although no significant differences were observed in many genes between the DEN+FF and DEN+FF+NAC groups, only glutathione peroxidase 2 (Gpx2) mRNA increased in the DEN+FF+NAC group as compared with the DEN+FF group. The results under the present experimental conditions indicate no obvious modifying effect of NAC on liver tumor promotion by FF in rats. The Japanese Society of Toxicologic Pathology 2009-12 2009-12-21 /pmc/articles/PMC3234604/ /pubmed/22272000 http://dx.doi.org/10.1293/tox.22.255 Text en 2009 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
Nishimura, Jihei
Dewa, Yasuaki
Jin, Meilan
Saegusa, Yukie
Kawai, Masaomi
Kemmochi, Sayaka
Shimamoto, Keisuke
Harada, Tomoaki
Itoh, Tadashi
Shima, Tomomi
Shibutani, Makoto
Mitsumori, Kunitoshi
No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats
title No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats
title_full No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats
title_fullStr No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats
title_full_unstemmed No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats
title_short No Modifying Effect of Antioxidant N-Acetyl-L-Cysteine on Fenofibrate-induced Hepatocarcinogenesis in Rats
title_sort no modifying effect of antioxidant n-acetyl-l-cysteine on fenofibrate-induced hepatocarcinogenesis in rats
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234604/
https://www.ncbi.nlm.nih.gov/pubmed/22272000
http://dx.doi.org/10.1293/tox.22.255
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