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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 |
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