Literature DB >> 2161167

Variation in drug-metabolizing enzyme activities during the growth of human Hep G2 hepatoma cells.

H Doostdar1, A Demoz, M D Burke, W T Melvin, M H Grant.   

Abstract

1. The activities of several drug-metabolizing enzymes change during the growth cycle (exponential growth to confluence) of Hep G2 cells in culture. As the rate of cell growth slowed down (days 7 to 10 after passage) the activities of ethoxy- and methoxy-resorufin O-dealkylase and of NADPH cytochrome c- and NADH cytochrome b5-reductase increased. In contrast, the O-dealkylations of pentoxy- and benzyloxy-resorufin did not change significantly during culture. 2. UDP-glucuronyltransferase activities also showed substrate-dependent alterations with time in culture. In contrast, glutathione-S-transferase activity remained constant despite a decline in the intracellular reduced glutathione content. 3. Epoxide hydrolase activity altered throughout time in culture, with an initial decrease in activity followed by a marked increase between days 7 and 10 after passage. 4. These results indicate the importance of standardizing the protocol with regard to the timing of experiments within the growth period of the cells when using hepatoma cell lines for assessing the metabolism and cytotoxicity of chemicals.

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Year:  1990        PMID: 2161167     DOI: 10.3109/00498259009046859

Source DB:  PubMed          Journal:  Xenobiotica        ISSN: 0049-8254            Impact factor:   1.908


  5 in total

1.  Modulation of the pentose phosphate pathway alters phase I metabolism of testosterone and dextromethorphan in HepG2 cells.

Authors:  Wen-jing Xiao; Ting Ma; Chun Ge; Wen-juan Xia; Yong Mao; Run-bin Sun; Xiao-yi Yu; Ji-ye Aa; Guang-ji Wang
Journal:  Acta Pharmacol Sin       Date:  2015-01-26       Impact factor: 6.150

2.  Prolonged lidocaine metabolizing activity of primary hepatocytes with spheroid culture using polyurethane foam as a culture substratum.

Authors:  K Nakazawa; T Matsushita; K Funatsu
Journal:  Cytotechnology       Date:  1997-09       Impact factor: 2.058

3.  Hydrogen peroxide- and cell-density-regulated expression of NADH-cytochrome b5 reductase in HeLa cells.

Authors:  Rosario I Bello; Francisco J Alcaín; Consuelo Gómez-Díaz; Guillermo López-Lluch; Plácido Navas; José M Villalba
Journal:  J Bioenerg Biomembr       Date:  2003-04       Impact factor: 2.945

4.  Primary hepatocytes outperform Hep G2 cells as the source of biotransformation functions in a bioartificial liver.

Authors:  S L Nyberg; R P Remmel; H J Mann; M V Peshwa; W S Hu; F B Cerra
Journal:  Ann Surg       Date:  1994-07       Impact factor: 12.969

5.  Dietary polyphenols protect against N-nitrosamines and benzo(a)pyrene-induced DNA damage (strand breaks and oxidized purines/pyrimidines) in HepG2 human hepatoma cells.

Authors:  Maria Eugenia Delgado; Ana Isabel Haza; Núria Arranz; Almudena García; Paloma Morales
Journal:  Eur J Nutr       Date:  2008-10-30       Impact factor: 5.614

  5 in total

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