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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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.
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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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