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Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes
Hepatocytes from male Spragne‐Dawley rats pretreated with a cytochrome P‐450 inducer, 3‐methoxy‐4‐aminoazobenzene (3‐MeO‐AAB), 3‐methylcholanthrene (MC) or phenobarbital (PB), were cultured in vitro, and changes in the quantity and activity of microsomal cytochrome P‐450 isozymes in the cells were d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1989
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917698/ https://www.ncbi.nlm.nih.gov/pubmed/2498247 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02279.x |
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author | Namiki, Masayuki Degawa, Masakuni Masuko, Takashi Hashimoto, Yoshiyuki |
author_facet | Namiki, Masayuki Degawa, Masakuni Masuko, Takashi Hashimoto, Yoshiyuki |
author_sort | Namiki, Masayuki |
collection | PubMed |
description | Hepatocytes from male Spragne‐Dawley rats pretreated with a cytochrome P‐450 inducer, 3‐methoxy‐4‐aminoazobenzene (3‐MeO‐AAB), 3‐methylcholanthrene (MC) or phenobarbital (PB), were cultured in vitro, and changes in the quantity and activity of microsomal cytochrome P‐450 isozymes in the cells were determined by means of immunochemical methods and a bacterial mutation test, respectively. The results of enzyme‐linked immunosorbent assay using monoclonal antibodies against rat P‐450 isozymes ‐ test using Salmonella typhimurium TA 98 and carcinogenic aromatic amines. These results indicate that microsomal cytochrome P‐450c in primary cultured rat hepatocytes is more stable in culture, in terms of both quantity and activity, than cytochrome P‐450d and P‐450b/e. |
format | Online Article Text |
id | pubmed-5917698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59176982018-05-11 Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes Namiki, Masayuki Degawa, Masakuni Masuko, Takashi Hashimoto, Yoshiyuki Jpn J Cancer Res Article Hepatocytes from male Spragne‐Dawley rats pretreated with a cytochrome P‐450 inducer, 3‐methoxy‐4‐aminoazobenzene (3‐MeO‐AAB), 3‐methylcholanthrene (MC) or phenobarbital (PB), were cultured in vitro, and changes in the quantity and activity of microsomal cytochrome P‐450 isozymes in the cells were determined by means of immunochemical methods and a bacterial mutation test, respectively. The results of enzyme‐linked immunosorbent assay using monoclonal antibodies against rat P‐450 isozymes ‐ test using Salmonella typhimurium TA 98 and carcinogenic aromatic amines. These results indicate that microsomal cytochrome P‐450c in primary cultured rat hepatocytes is more stable in culture, in terms of both quantity and activity, than cytochrome P‐450d and P‐450b/e. Blackwell Publishing Ltd 1989-02 /pmc/articles/PMC5917698/ /pubmed/2498247 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02279.x Text en |
spellingShingle | Article Namiki, Masayuki Degawa, Masakuni Masuko, Takashi Hashimoto, Yoshiyuki Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes |
title | Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes |
title_full | Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes |
title_fullStr | Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes |
title_full_unstemmed | Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes |
title_short | Changes in the Quantity and Activity of Cytochrome P‐450 Isozymes in Primary Cultured Rat Hepatocytes |
title_sort | changes in the quantity and activity of cytochrome p‐450 isozymes in primary cultured rat hepatocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917698/ https://www.ncbi.nlm.nih.gov/pubmed/2498247 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02279.x |
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