Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7256
Title: In vivo effects of Urtica urens (dwarf nettle) on the expression of CYP1A in control and 3-methylcholanthrene-exposed rats
Authors: Ozkarsli, M.
Sevim, H.
Şen, Alaattin.
Keywords: 3-methylcholanthrene
7-ethoxyresorufin O-deethylase (EROD)
7-methoxyresorufin O-demethylase (MROD)
Chemoprotection
CYP1A
Urtica urens
3 methylcholanthrene
carcinogen
cytochrome P450 1A
cytochrome P450 1A2
ethoxyresorufin deethylase
messenger RNA
unclassified drug
Urtica extract
Urtica urens extract
animal experiment
animal model
animal tissue
article
body weight
controlled study
enzyme active site
enzyme activity
gene expression
kidney
liver
lung
male
medicinal plant
nonhuman
plant seed
protein expression
rat
reverse transcription polymerase chain reaction
Western blotting
Wistar rat
Animals
Carcinogens
Cytochrome P-450 CYP1A1
Cytochrome P-450 CYP1A2
Kidney
Liver
Lung
Male
Methylcholanthrene
Plant Extracts
Rats
Rats, Wistar
RNA, Messenger
Urticaceae
Rattus
Rattus norvegicus
Urtica
Abstract: The in vivo effects of the intraperitoneal administration of an Urtica urens L. (dwarf nettle) seed extract were examined on the hepatic, pulmonary, and renal cytochrome P450-dependent monooxygenase activities of rats co-administered with 3-methylcholanthrene (MC). Urtica extract was administered by intraperitoneal injection to male Wistar rats at 200mgkg-1day-1 for 4 days from which were also co-administered with intraperitoneal injection of 50mg of MCkg-1 of body weight twice on days 1 and 3. MC treatment increased the 7-ethoxyresorufin O-deethylase (EROD) activity of the liver, lung, and kidney 54-, 21-, and 119-fold, respectively. Urtica treatment substantially reduced the 3MC induction of hepatic, lung, and renal EROD activity by 79, 42, and 50%, respectively. Similarly, compared with the control, MROD activities in liver and kidney were increased after MC administration, and these increases were significantly inhibited by Urtica. reverse transcriptase-polymerase chain reaction (RT-PCR) analysis clearly showed that the hepatic CYP1A1 and CYP1A2 mRNA levels substantially increased after treatment with MC, which was suppressed by Urtica supplementation. Western blotting studies also supported the alterations observed in the catalytic activities and mRNA levels. In conclusion, substantial reduction in CYP1A1 and CYP1A2 expression levels and related activities with Urtica are possibly associated with a potential chemoprotective ability of the Urtica due to the anticipated decrease in the activation of environmental chemical carcinogens through modulation of the CYP1A enzymes. © 2008 Informa UK Ltd.
URI: https://hdl.handle.net/11499/7256
https://doi.org/10.1080/00498250701713968
ISSN: 0049-8254
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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