Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8127
Title: Epilobium hirsutum alters xenobiotic metabolizing CYP1A1, CYP2E1, NQO1 and GPx activities, mRNA and protein levels in rats
Authors: Karakurt, S.
Semiz, Aslı
Çelik, Gurbet
Gencler-Ozkan, A.M.
Sen, A.
Adali, O.
Keywords: Cytochrome P450
Drug metabolism
Glutathione peroxidase
Liver enzymes
Medicinal plant
NQO1
Onagraceae
cytochrome P450 1A1
cytochrome P450 2E1
Epilobium hirsutum extract
ethoxyresorufin deethylase
glutathione peroxidase
messenger RNA
nadph quinone oxidoreductase 1
natural product
oxygenase
reduced nicotinamide adenine dinucleotide dehydrogenase (ubiquinone)
unclassified drug
animal experiment
animal model
animal tissue
article
controlled study
drug mechanism
drug metabolism
enzyme activity
enzyme metabolism
Epilobium
epilobium hirsutum
in vivo study
liver level
male
nonhuman
phytochemistry
protein expression
rat
xenobiotic metabolism
Animals
Blotting, Western
Cytochrome P-450 CYP1A1
Cytochrome P-450 CYP2E1
Gene Expression Regulation
Glutathione Peroxidase
Injections, Intraperitoneal
Liver
Male
NAD(P)H Dehydrogenase (Quinone)
Plant Extracts
Polymerase Chain Reaction
Rats
Rats, Wistar
RNA, Messenger
Xenobiotics
Animalia
Epilobium hirsutum
Rattus
Abstract: Context: Natural products have attracted increasing interests due to their use in flavoring, nutrition, cosmetics, pharmacy and medicine. Epilobium hirsutum L. (Onagraceae) is known for its analgesic, antimicrobial, and antiproliferative activity. CYP1A1 and CYP2E1, xenobiotic metabolizing enzymes, serve as a metabolic activation route yielding reactive metabolites that are eliminated by the action of NQO1 and glutathione peroxidase (GPx) enzymes. Objective: This study investigated in vivo effects of Epilobium hirsutum (EH) on CYP2E1, CYP1A1, NQO1 and GPx activities, protein and mRNA expressions in liver. Materials and methods: Male Wistar Albino rats were injected with EH at a dose of 37.5mg/kg i.p. daily for 9d. CYP2E1, CYP1A1, NQO1 and GPx activities, protein and mRNA levels were determined by enzyme assays, Western blotting and qPCR, respectively. Results: CYP1A1 associated ethoxyresorufin-O-deethylase activity of control and EH-treated animals were found as 6.54±1.21 and 4.48±1.67nmol/min/mg, respectively. CYP2E1 associated aniline 4-hydroxylase of control and EH group were 0.537±0.011 and 0.109±0.01nmol/min/mg, respectively. However, EH treatment increased the GPx and NQO1 activities from 0.069±0.015 to 0.107±0.026nmol/min/mg and from 163.34±92 to 588.3±14nmol/min/mg, respectively. Furthermore, protein and mRNA expression analysis revealed that CYP1A1 and CYP2E1 levels were decreased while those of NQO1 and GPx increased after EH treatment. Discussion and conclusion: Our current data suggest that the metabolism of xenobiotics, including drugs, may be altered due to changes in the expression and activity of these proteins by EH. © 2013 Informa Healthcare USA, Inc.
URI: https://hdl.handle.net/11499/8127
https://doi.org/10.3109/13880209.2012.762404
ISSN: 1388-0209
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Teknoloji Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

Files in This Item:
File SizeFormat 
10.3109 13880209.2012.762404.pdf772.32 kBAdobe PDFView/Open
Show full item record



CORE Recommender

SCOPUSTM   
Citations

17
checked on Dec 14, 2024

WEB OF SCIENCETM
Citations

13
checked on Dec 20, 2024

Page view(s)

50
checked on Aug 24, 2024

Download(s)

34
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.