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Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo
The lack of information concerning individual variation in content and activity of human liver microsomal protein is one of the most important obstacles for designing personalized medicines. We demonstrated that the mean value of microsomal protein per gram of liver (MPPGL) was 39.46 mg/g in 128 hum...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669488/ https://www.ncbi.nlm.nih.gov/pubmed/26635233 http://dx.doi.org/10.1038/srep17671 |
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author | Zhang, Haifeng Gao, Na Tian, Xin Liu, Tingting Fang, Yan Zhou, Jun Wen, Qiang Xu, Binbin Qi, Bing Gao, Jie Li, Hongmeng Jia, Linjing Qiao, Hailing |
author_facet | Zhang, Haifeng Gao, Na Tian, Xin Liu, Tingting Fang, Yan Zhou, Jun Wen, Qiang Xu, Binbin Qi, Bing Gao, Jie Li, Hongmeng Jia, Linjing Qiao, Hailing |
author_sort | Zhang, Haifeng |
collection | PubMed |
description | The lack of information concerning individual variation in content and activity of human liver microsomal protein is one of the most important obstacles for designing personalized medicines. We demonstrated that the mean value of microsomal protein per gram of liver (MPPGL) was 39.46 mg/g in 128 human livers and up to 19-fold individual variations existed. Meanwhile, the metabolic activities of 10 cytochrome P450 (CYPs) were detected in microsomes and liver tissues, respectively, which showed huge individual variations (200-fold). Compared with microsomes, the activities of liver tissues were much suitable to express the individual variations of CYP activities. Furthermore, individual variations in the in vivo clearance of tolbutamide were successfully predicted with the individual parameter values. In conclusion, we offer the values for MPPGL contents in normal liver tissues and build a new method to assess the in vitro CYP activities. In addition, large individual variations exist in predicted hepatic clearance of tolbutamide. These findings provide important physiological parameters for physiologically-based pharmacokinetics models and thus, establish a solid foundation for future development of personalized medicines. |
format | Online Article Text |
id | pubmed-4669488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46694882015-12-11 Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo Zhang, Haifeng Gao, Na Tian, Xin Liu, Tingting Fang, Yan Zhou, Jun Wen, Qiang Xu, Binbin Qi, Bing Gao, Jie Li, Hongmeng Jia, Linjing Qiao, Hailing Sci Rep Article The lack of information concerning individual variation in content and activity of human liver microsomal protein is one of the most important obstacles for designing personalized medicines. We demonstrated that the mean value of microsomal protein per gram of liver (MPPGL) was 39.46 mg/g in 128 human livers and up to 19-fold individual variations existed. Meanwhile, the metabolic activities of 10 cytochrome P450 (CYPs) were detected in microsomes and liver tissues, respectively, which showed huge individual variations (200-fold). Compared with microsomes, the activities of liver tissues were much suitable to express the individual variations of CYP activities. Furthermore, individual variations in the in vivo clearance of tolbutamide were successfully predicted with the individual parameter values. In conclusion, we offer the values for MPPGL contents in normal liver tissues and build a new method to assess the in vitro CYP activities. In addition, large individual variations exist in predicted hepatic clearance of tolbutamide. These findings provide important physiological parameters for physiologically-based pharmacokinetics models and thus, establish a solid foundation for future development of personalized medicines. Nature Publishing Group 2015-12-04 /pmc/articles/PMC4669488/ /pubmed/26635233 http://dx.doi.org/10.1038/srep17671 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhang, Haifeng Gao, Na Tian, Xin Liu, Tingting Fang, Yan Zhou, Jun Wen, Qiang Xu, Binbin Qi, Bing Gao, Jie Li, Hongmeng Jia, Linjing Qiao, Hailing Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
title | Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
title_full | Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
title_fullStr | Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
title_full_unstemmed | Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
title_short | Content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
title_sort | content and activity of human liver microsomal protein and prediction of individual hepatic clearance in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669488/ https://www.ncbi.nlm.nih.gov/pubmed/26635233 http://dx.doi.org/10.1038/srep17671 |
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