Effects of total parenteral nutrition on drug metabolism gene expression in mice
Parenteral nutrition-associated liver disease (PNALD) is a liver dysfunction caused by various risk factors presented in patients receiving total parenteral nutrition (TPN). Omega-6 rich Intralipid® and omega-3 rich Omegaven® are two intravenous lipid emulsions used in TPN. TPN could affect the hepa...
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doaj-f6377ca2c73543e1bea80cbeaf5795da2020-11-25T02:38:46ZengElsevierActa Pharmaceutica Sinica B2211-38352020-01-01101153158Effects of total parenteral nutrition on drug metabolism gene expression in miceChristina Ferrucci-Da Silva0Le Zhan1Jianliang Shen2Bo Kong3Michael J. Campbell4Naureen Memon5Thomas Hegyi6Lucy Lu7Grace L. Guo8Division of Neonatology, Department of Pediatrics, Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USARutgers Cancer Institute of New Jersey, New Brunswick, NJ 08901, USADepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854, USADepartment of Pharmacology and Toxicology, School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USADepartment of Pharmacology and Toxicology, School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USAMidAtlantic Neonatology Associates, Morristown, NJ 07960, USADivision of Neonatology, Department of Pediatrics, Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USASchool of Pharmacy, University of Pittsburgh, Pittsburgh, PA 15260, USADepartment of Pharmacology and Toxicology, School of Pharmacy, Rutgers University, Piscataway, NJ 08854, USA; Environmental and Occupational Health Institute, Rutgers University, Piscataway, NJ 08854, USA; VA NJ Health Care Systems, East Orange, NJ 07018, USA; Corresponding author.Parenteral nutrition-associated liver disease (PNALD) is a liver dysfunction caused by various risk factors presented in patients receiving total parenteral nutrition (TPN). Omega-6 rich Intralipid® and omega-3 rich Omegaven® are two intravenous lipid emulsions used in TPN. TPN could affect the hepatic expression of genes in anti-oxidative stress, but it's unknown whether TPN affects genes in drug metabolism. In this study, either Intralipid®- or Omegaven®-based TPN was administered to mice and the expression of a cohort of genes involved in anti-oxidative stress or drug metabolism was analyzed, glutathione (GSH) levels were measured, and protein levels for two key drug metabolism genes were determined. Overall, the expression of most genes was downregulated by Intralipid®-based TPN (Gstp1, Gstm1, 3, 6, Nqo1, Ho-1, Mt-1, Gclc, Gclm, Cyp2d9, 2f2, 2b10, and 3a11). Omegaven® showed similar results as Intralipid® except for preserving the expression of Gstm1 and Cyp3a11, and increasing Ho-1. Total GSH levels were decreased by Intralipid®, but increased by Omegaven®. CYP3A11 protein levels were increased by Omegaven®. In conclusion, TPN reduced the expression of many genes involved in anti-oxidative stress and drug metabolism in mice. However, Omegaven® preserved expression of Cyp3a11, suggesting another beneficial effect of Omegaven® in protecting liver functions. Key words: Total parenteral nutrition, Glutathione, Drug metabolism, Liver, Parenteral nutrition-associated liver diseasehttp://www.sciencedirect.com/science/article/pii/S2211383519309773 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Christina Ferrucci-Da Silva Le Zhan Jianliang Shen Bo Kong Michael J. Campbell Naureen Memon Thomas Hegyi Lucy Lu Grace L. Guo |
spellingShingle |
Christina Ferrucci-Da Silva Le Zhan Jianliang Shen Bo Kong Michael J. Campbell Naureen Memon Thomas Hegyi Lucy Lu Grace L. Guo Effects of total parenteral nutrition on drug metabolism gene expression in mice Acta Pharmaceutica Sinica B |
author_facet |
Christina Ferrucci-Da Silva Le Zhan Jianliang Shen Bo Kong Michael J. Campbell Naureen Memon Thomas Hegyi Lucy Lu Grace L. Guo |
author_sort |
Christina Ferrucci-Da Silva |
title |
Effects of total parenteral nutrition on drug metabolism gene expression in mice |
title_short |
Effects of total parenteral nutrition on drug metabolism gene expression in mice |
title_full |
Effects of total parenteral nutrition on drug metabolism gene expression in mice |
title_fullStr |
Effects of total parenteral nutrition on drug metabolism gene expression in mice |
title_full_unstemmed |
Effects of total parenteral nutrition on drug metabolism gene expression in mice |
title_sort |
effects of total parenteral nutrition on drug metabolism gene expression in mice |
publisher |
Elsevier |
series |
Acta Pharmaceutica Sinica B |
issn |
2211-3835 |
publishDate |
2020-01-01 |
description |
Parenteral nutrition-associated liver disease (PNALD) is a liver dysfunction caused by various risk factors presented in patients receiving total parenteral nutrition (TPN). Omega-6 rich Intralipid® and omega-3 rich Omegaven® are two intravenous lipid emulsions used in TPN. TPN could affect the hepatic expression of genes in anti-oxidative stress, but it's unknown whether TPN affects genes in drug metabolism. In this study, either Intralipid®- or Omegaven®-based TPN was administered to mice and the expression of a cohort of genes involved in anti-oxidative stress or drug metabolism was analyzed, glutathione (GSH) levels were measured, and protein levels for two key drug metabolism genes were determined. Overall, the expression of most genes was downregulated by Intralipid®-based TPN (Gstp1, Gstm1, 3, 6, Nqo1, Ho-1, Mt-1, Gclc, Gclm, Cyp2d9, 2f2, 2b10, and 3a11). Omegaven® showed similar results as Intralipid® except for preserving the expression of Gstm1 and Cyp3a11, and increasing Ho-1. Total GSH levels were decreased by Intralipid®, but increased by Omegaven®. CYP3A11 protein levels were increased by Omegaven®. In conclusion, TPN reduced the expression of many genes involved in anti-oxidative stress and drug metabolism in mice. However, Omegaven® preserved expression of Cyp3a11, suggesting another beneficial effect of Omegaven® in protecting liver functions. Key words: Total parenteral nutrition, Glutathione, Drug metabolism, Liver, Parenteral nutrition-associated liver disease |
url |
http://www.sciencedirect.com/science/article/pii/S2211383519309773 |
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