CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro
In this study, we investigated the enzymes catalyzing the phaseⅠmetabolism of thiacalixarene (TCAS) based on in vitro system including cDNA-expressed P450 enzymes, human liver microsomes plus inhibitors and monoclonal antibodies. In addition, the inhibitory potential of TCAS on major CYP450 drug met...
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doaj-d43b8237cc66428fa40c2acb0222e2b22020-11-25T00:50:24ZengMDPI AGInternational Journal of Environmental Research and Public Health1660-46012015-09-01129107831079310.3390/ijerph120910783ijerph120910783CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in VitroGuolin Shen0Cheng Wang1Lili Zhou2Lei Li3Huiming Chen4Wenlian Yu5Haishan Li6Chinese Academy of Inspection and Quarantine, Beijing 100123, ChinaChinese Academy of Inspection and Quarantine, Beijing 100123, ChinaChinese Academy of Inspection and Quarantine, Beijing 100123, ChinaChinese Academy of Inspection and Quarantine, Beijing 100123, ChinaChinese Academy of Inspection and Quarantine, Beijing 100123, ChinaChinese Academy of Inspection and Quarantine, Beijing 100123, ChinaChinese Academy of Inspection and Quarantine, Beijing 100123, ChinaIn this study, we investigated the enzymes catalyzing the phaseⅠmetabolism of thiacalixarene (TCAS) based on in vitro system including cDNA-expressed P450 enzymes, human liver microsomes plus inhibitors and monoclonal antibodies. In addition, the inhibitory potential of TCAS on major CYP450 drug metabolizing enzymes (CYP1A2, CYP2C9, CYP2B6, CYP2D6 and CYP3A4) was assessed. The results showed that CYP1A2 and CYP2C9 mediated TCAS hydroxylation. IC50 values for TCAS in rat and human liver microsomes were greater than 50 µM, and it demonstrated a weak inhibition of rat and human CYP450 enzymes. Finally, sandwiched hepatocytes were used to evaluate the induction of CYP1A and CYP3A to define the function of TCAS in vivo. The results showed that incubation of TCAS at different concentrations for 72 h failed to induce CYP1A and CYP3A. However, incubation of the cells with 50 and 100 µM TCAS caused a profound decrease in the activities of CYP1A and CYP3A, which was probably due to cytotoxic effects, suggesting that exposure to TCAS might be a health concern.http://www.mdpi.com/1660-4601/12/9/10783thiacalix[4]arene tetrasulfonateCYP450hepatocytemetabolism |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Guolin Shen Cheng Wang Lili Zhou Lei Li Huiming Chen Wenlian Yu Haishan Li |
spellingShingle |
Guolin Shen Cheng Wang Lili Zhou Lei Li Huiming Chen Wenlian Yu Haishan Li CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro International Journal of Environmental Research and Public Health thiacalix[4]arene tetrasulfonate CYP450 hepatocyte metabolism |
author_facet |
Guolin Shen Cheng Wang Lili Zhou Lei Li Huiming Chen Wenlian Yu Haishan Li |
author_sort |
Guolin Shen |
title |
CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro |
title_short |
CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro |
title_full |
CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro |
title_fullStr |
CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro |
title_full_unstemmed |
CYP450 Enzyme-Mediated Metabolism of TCAS and Its Inhibitory and Induced Effects on Metabolized Enzymes in Vitro |
title_sort |
cyp450 enzyme-mediated metabolism of tcas and its inhibitory and induced effects on metabolized enzymes in vitro |
publisher |
MDPI AG |
series |
International Journal of Environmental Research and Public Health |
issn |
1660-4601 |
publishDate |
2015-09-01 |
description |
In this study, we investigated the enzymes catalyzing the phaseⅠmetabolism of thiacalixarene (TCAS) based on in vitro system including cDNA-expressed P450 enzymes, human liver microsomes plus inhibitors and monoclonal antibodies. In addition, the inhibitory potential of TCAS on major CYP450 drug metabolizing enzymes (CYP1A2, CYP2C9, CYP2B6, CYP2D6 and CYP3A4) was assessed. The results showed that CYP1A2 and CYP2C9 mediated TCAS hydroxylation. IC50 values for TCAS in rat and human liver microsomes were greater than 50 µM, and it demonstrated a weak inhibition of rat and human CYP450 enzymes. Finally, sandwiched hepatocytes were used to evaluate the induction of CYP1A and CYP3A to define the function of TCAS in vivo. The results showed that incubation of TCAS at different concentrations for 72 h failed to induce CYP1A and CYP3A. However, incubation of the cells with 50 and 100 µM TCAS caused a profound decrease in the activities of CYP1A and CYP3A, which was probably due to cytotoxic effects, suggesting that exposure to TCAS might be a health concern. |
topic |
thiacalix[4]arene tetrasulfonate CYP450 hepatocyte metabolism |
url |
http://www.mdpi.com/1660-4601/12/9/10783 |
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