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  1. Article ; Online: Endosulfan induces CYP2B6 and CYP3A4 by activating the pregnane X receptor.

    Casabar, Richard C T / Das, Parikshit C / Dekrey, Gregory K / Gardiner, Catherine S / Cao, Yan / Rose, Randy L / Wallace, Andrew D

    Toxicology and applied pharmacology

    2010  Volume 245, Issue 3, Page(s) 335–343

    Abstract: Endosulfan is an organochlorine pesticide commonly used in agriculture. Endosulfan has affects on vertebrate xenobiotic metabolism pathways that may be mediated, in part, by its ability to activate the pregnane X receptor (PXR) and/or the constitutive ... ...

    Abstract Endosulfan is an organochlorine pesticide commonly used in agriculture. Endosulfan has affects on vertebrate xenobiotic metabolism pathways that may be mediated, in part, by its ability to activate the pregnane X receptor (PXR) and/or the constitutive androstane receptor (CAR) which can elevate expression of cytochrome P450 (CYP) enzymes. This study examined the dose-dependency and receptor specificity of CYP induction in vitro and in vivo. The HepG2 cell line was transiently transfected with CYP2B6- and CYP3A4-luciferase promoter reporter plasmids along with human PXR (hPXR) or hCAR expression vectors. In the presence of hPXR, endosulfan-alpha exposure caused significant induction of CYP2B6 (16-fold) and CYP3A4 (11-fold) promoter activities over control at 10 microM. The metabolite endosulfan sulfate also induced CYP2B6 (12-fold) and CYP3A4 (6-fold) promoter activities over control at 10 microM. In the presence of hCAR-3, endosulfan-alpha induced CYP2B6 (2-fold) promoter activity at 10 microM, but not at lower concentrations. These data indicate that endosulfan-alpha significantly activates hPXR strongly and hCAR weakly. Using western blot analysis of human hepatocytes, the lowest concentrations at which CYP2B6 and CYP3A4 protein levels were found to be significantly elevated by endosulfan-alpha were 1.0 microM and 10 microM, respectively. In mPXR-null/hPXR-transgenic mice, endosulfan-alpha exposure (2.5mg/kg/day) caused a significant reduction of tribromoethanol-induced sleep times by approximately 50%, whereas no significant change in sleep times was observed in PXR-null mice. These data support the role of endosulfan-alpha as a strong activator of PXR and inducer of CYP2B6 and CYP3A4, which may impact metabolism of CYP2B6 or CYP3A4 substrates.
    MeSH term(s) Anesthetics/metabolism ; Anesthetics/pharmacology ; Animals ; Apoptosis/drug effects ; Aryl Hydrocarbon Hydroxylases/biosynthesis ; Aryl Hydrocarbon Hydroxylases/genetics ; Cytochrome P-450 CYP2B6 ; Cytochrome P-450 CYP3A/biosynthesis ; Cytochrome P-450 CYP3A/genetics ; Cytochrome P-450 Enzyme System/biosynthesis ; Dose-Response Relationship, Drug ; Endosulfan/toxicity ; Enzyme Induction ; Ethanol/analogs & derivatives ; Ethanol/metabolism ; Ethanol/pharmacology ; Genes, Reporter ; Hep G2 Cells ; Hepatocytes/drug effects ; Hepatocytes/enzymology ; Humans ; Insecticides/toxicity ; Luciferases/biosynthesis ; Luciferases/genetics ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Oxidoreductases, N-Demethylating/biosynthesis ; Oxidoreductases, N-Demethylating/genetics ; Pregnane X Receptor ; Promoter Regions, Genetic/drug effects ; RNA, Messenger/metabolism ; Receptors, Cytoplasmic and Nuclear/agonists ; Receptors, Cytoplasmic and Nuclear/genetics ; Receptors, Cytoplasmic and Nuclear/metabolism ; Receptors, Steroid/agonists ; Receptors, Steroid/genetics ; Receptors, Steroid/metabolism ; Sleep/drug effects ; Time Factors ; Transfection
    Chemical Substances Anesthetics ; Insecticides ; Pregnane X Receptor ; RNA, Messenger ; Receptors, Cytoplasmic and Nuclear ; Receptors, Steroid ; tribromoethanol (149JI83A44) ; Ethanol (3K9958V90M) ; constitutive androstane receptor (438XLITDI3) ; Cytochrome P-450 Enzyme System (9035-51-2) ; Luciferases (EC 1.13.12.-) ; Aryl Hydrocarbon Hydroxylases (EC 1.14.14.1) ; CYP2B6 protein, human (EC 1.14.14.1) ; CYP3A protein, mouse (EC 1.14.14.1) ; Cytochrome P-450 CYP2B6 (EC 1.14.14.1) ; Cytochrome P-450 CYP3A (EC 1.14.14.1) ; CYP3A4 protein, human (EC 1.14.14.55) ; Oxidoreductases, N-Demethylating (EC 1.5.-) ; Endosulfan (OKA6A6ZD4K)
    Language English
    Publishing date 2010-03-31
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 204477-8
    ISSN 1096-0333 ; 0041-008X
    ISSN (online) 1096-0333
    ISSN 0041-008X
    DOI 10.1016/j.taap.2010.03.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Effects of paraquat on development of preimplantation embryos in vivo and in vitro.

    Hausburg, Mellisa A / Dekrey, Gregory K / Salmen, James J / Palic, Michelle R / Gardiner, Catherine S

    Reproductive toxicology (Elmsford, N.Y.)

    2005  Volume 20, Issue 2, Page(s) 239–246

    Abstract: Paraquat can cause oxidative stress through redox cycling, and preimplantation embryos are sensitive to oxidative stress in vitro. In this study, the effects of paraquat on preimplantation embryo development were examined. Exposure of preimplantation ... ...

    Abstract Paraquat can cause oxidative stress through redox cycling, and preimplantation embryos are sensitive to oxidative stress in vitro. In this study, the effects of paraquat on preimplantation embryo development were examined. Exposure of preimplantation embryos (collected on the day after ovulation) to paraquat in vitro for 24 h at concentrations as low as 8 microM caused a significant decrease in the percentage of 8-cell embryos and an increase in the percentage of compacted morulae, but the content of reduced glutathione (GSH) in embryos was not changed. Altered embryo development was most likely due to premature compaction because a 42% decrease in cell number per compacted morulae was observed in embryos exposed to paraquat at 1 mM. Exposure of preimplantation embryos to paraquat in vitro for 4 days at 200 microM or higher eliminated development beyond the blastocyst stage. Exposure of bred female mice to paraquat at 30 mg/kg on day 2 after ovulation led to a small but significant decrease in the percentage of 8-cell embryos on day 3 without a detectable increase in the percentage of compacted morulae. No detectable change in preimplantation embryo development was found following paraquat exposure on the day of ovulation (day 0), although a significant decrease in embryo GSH was found on day 1. These data indicate that paraquat can adversely impact the development of preimplantation embryos in vitro and in vivo without consistent modulation of GSH level.
    MeSH term(s) Animals ; Animals, Outbred Strains ; Blastocyst/cytology ; Blastocyst/drug effects ; Blastocyst/metabolism ; Cells, Cultured ; Dose-Response Relationship, Drug ; Embryonic Development ; Female ; Glutathione/analysis ; Glutathione/metabolism ; Herbicides/pharmacology ; Injections, Intraperitoneal ; Mice ; Microscopy, Fluorescence ; Morula/drug effects ; Paraquat/pharmacology ; Pregnancy ; Time Factors
    Chemical Substances Herbicides ; Glutathione (GAN16C9B8O) ; Paraquat (PLG39H7695)
    Language English
    Publishing date 2005-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 639342-1
    ISSN 1873-1708 ; 0890-6238
    ISSN (online) 1873-1708
    ISSN 0890-6238
    DOI 10.1016/j.reprotox.2005.03.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) reduces Leishmania major burdens in C57BL/6 mice.

    Bowers, Owen J / Sommersted, Kirsa B / Sowell, Ryan T / Boling, Gretchen E / Hanneman, William H / Titus, Richard G / Dekrey, Gregory K

    The American journal of tropical medicine and hygiene

    2006  Volume 75, Issue 4, Page(s) 749–752

    Abstract: Acute exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) can suppress adaptive immunity. In this study, pre-exposure of Leishmania major-infected mice to TCDD caused a dose-dependent and unexpected decrease in parasite burdens on day 20 after ... ...

    Abstract Acute exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) can suppress adaptive immunity. In this study, pre-exposure of Leishmania major-infected mice to TCDD caused a dose-dependent and unexpected decrease in parasite burdens on day 20 after infection. In contrast, TCDD-mediated lymphoid atrophy, suppressed antibody levels, and enhanced interleukin-2 production were observed as expected. These results suggest that TCDD may enhance resistance to L. major in the face of immune suppression.
    MeSH term(s) Animals ; Antibodies, Protozoan/blood ; Antibodies, Protozoan/drug effects ; Cytokines/biosynthesis ; Cytokines/drug effects ; Dose-Response Relationship, Drug ; Environmental Pollutants/pharmacology ; Immunity, Cellular/drug effects ; Leishmania major/drug effects ; Leishmania major/growth & development ; Leishmania major/immunology ; Leishmaniasis, Cutaneous/immunology ; Leishmaniasis, Cutaneous/parasitology ; Mice ; Mice, Inbred C57BL ; Polychlorinated Dibenzodioxins/pharmacology
    Chemical Substances Antibodies, Protozoan ; Cytokines ; Environmental Pollutants ; Polychlorinated Dibenzodioxins
    Language English
    Publishing date 2006-10
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    Database MEDical Literature Analysis and Retrieval System OnLINE

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