Proteomic analysis of small intestinal epithelial cells in antibiotic-treated mice: Changes in drug transporters and metabolizing enzymes.
ATP Binding Cassette Transporter, Subfamily B, Member 1
/ analysis
Administration, Oral
Animals
Anti-Bacterial Agents
/ administration & dosage
Epithelial Cells
/ drug effects
Glutathione Transferase
/ analysis
Intestine, Small
/ cytology
Male
Mice
Mice, Inbred C57BL
Multidrug Resistance-Associated Protein 2
Multidrug Resistance-Associated Proteins
/ analysis
Peptide Transporter 1
/ analysis
Polymyxin B
/ administration & dosage
Proteomics
Vancomycin
/ administration & dosage
Antibiotics
Drug metabolizing enzyme
Drug transporter
Intestinal flora
Proteomics
Small intestine
Journal
Drug metabolism and pharmacokinetics
ISSN: 1880-0920
Titre abrégé: Drug Metab Pharmacokinet
Pays: England
ID NLM: 101164773
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
25
09
2018
revised:
16
12
2018
accepted:
08
01
2019
pubmed:
4
3
2019
medline:
26
7
2019
entrez:
4
3
2019
Statut:
ppublish
Résumé
Antibiotics act on bacterial flora originally present in the intestine, and changes in the intestinal flora have various effects on the host. This study investigated changes in the protein levels of drug transporters and metabolizing enzymes in the small intestines of antibiotic-treated mice by proteomic analysis. After the oral administration of non-absorbable antibiotics (vancomycin and polymyxin B) for 5 days, 15 drug transporter or metabolizing enzyme proteins had significantly changed levels among 1780 proteins identified in small intestinal epithelial cells. Of these, the levels of peptide transporter 1 (Pept1), multidrug resistance protein 1a (Mdr1a), and multidrug resistance-associated protein 2 (Mrp2) were increased approximately 2-fold. In addition, the levels of two Cyp4f proteins were decreased and those of Cyp4b1, Ces1d, and three glutathione S-transferase (Gst) proteins were increased. Our results indicate that the oral administration of antibiotics changes the levels of proteins related to the absorption and metabolism of drugs in the small intestine, and suggest that substrate drugs of these proteins have a risk for indirect drug interactions with antibacterial drugs via the intestinal flora.
Identifiants
pubmed: 30826185
pii: S1347-4367(18)30434-8
doi: 10.1016/j.dmpk.2019.01.001
pii:
doi:
Substances chimiques
ATP Binding Cassette Transporter, Subfamily B, Member 1
0
Anti-Bacterial Agents
0
Multidrug Resistance-Associated Protein 2
0
Multidrug Resistance-Associated Proteins
0
Peptide Transporter 1
0
Vancomycin
6Q205EH1VU
Glutathione Transferase
EC 2.5.1.18
Polymyxin B
J2VZ07J96K
Types de publication
Journal Article
Langues
eng
Pagination
159-162Informations de copyright
Copyright © 2019 The Japanese Society for the Study of Xenobiotics. Published by Elsevier Ltd. All rights reserved.