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Permanent link (DOI): https://doi.org/10.7939/R3XD0R86Z

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Differential Modulation of Aryl Hydrocarbon Receptor Regulated Genes by Chromium Open Access

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Other title
Subject/Keyword
Chromium
Aryl Hydrocarbon Receptor
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Asiri, Abdulrahman Y
Supervisor and department
El-Kadi, Ayman (Faculty of Pharmacy and Pharmaceutical Sciences)
Examining committee member and department
Baker, Glen (Faculty of Psychiatry)
El-Kadi, Ayman (Faculty of Pharmacy and Pharmaceutical Sciences)
Siraki, Arno (Faculty of Pharmacy and Pharmaceutical Sciences)
Department
Faculty of Pharmacy and Pharmaceutical Sciences
Specialization
Pharmaceutical Sciences
Date accepted
2015-06-17T16:02:28Z
Graduation date
2015-11
Degree
Master of Science
Degree level
Master's
Abstract
Several studies have examined the toxic effects of individual aryl hydrocarbon receptor (AhR) ligands, yet there are relatively few reports of the combined toxic effects of AhR ligands and other environmental co-contaminants, such as heavy metals. Chromium (Cr+6) is one of the major environmental toxic metal contaminants and a potent human toxin, mutagen, and carcinogen. Heavy metals alter the carcinogenicity of AhR ligands by modulating the cytochrome P450 1 (Cyp1) enzyme; however, the mechanism(s) remain unresolved. The objective of the current study was to investigate the effect of Cr+6 on expression and activity, of Cyp1a1, NQO1 and HO-1 in C57BL/6 mouse liver. C57BL/6 mice were injected intraperitoneally with Cr+6 (20 mg/kg) in the absence and presence of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) (15 μg/kg) for 24 h. The mice were segregated into 4 experimental groups. The first group was control mice, and they received saline plus corn oil. The second group was Cr+6-treated mice, and they received Cr+6 dissolved in saline plus corn oil. The third group was TCDD-treated mice, and they received TCDD dissolved in corn oil plus saline. The fourth group was Cr+6 plus TCDD–treated mice, and they received Cr+6 dissolved in saline plus TCDD dissolved in corn oil. Moreover, real-time PCR and Western blot were used to measure mRNA and protein expression, respectively. EROD was used to measure Cyp1a1 activity. Cr+6 alone did not significantly alter Cyp1a1, NQO1 or HO-1 at mRNA, protein, or catalytic activity levels. Upon co-exposure to Cr+6 and TCDD, Cr+6 significantly inhibited the TCDD-mediated induction of the Cyp1a1 mRNA, protein, or catalytic activity levels, whereas it significantly potentiated the induction of NQO1 and HO-1 mediated by TCDD at the mRNA, protein and catalytic activity levels at 24 h. We demonstrated that Cr+6 inhibits the AhR-ligand -mediated effect on the carcinogen-activating enzymes whereas it potentiated the carcinogen detoxifying enzymes NQO1 and HO-1.
Language
English
DOI
doi:10.7939/R3XD0R86Z
Rights
Permission is hereby granted to the University of Alberta Libraries to reproduce single copies of this thesis and to lend or sell such copies for private, scholarly or scientific research purposes only. The author reserves all other publication and other rights in association with the copyright in the thesis and, except as herein before provided, neither the thesis nor any substantial portion thereof may be printed or otherwise reproduced in any material form whatsoever without the author's prior written permission.
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