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1.
J Biochem Mol Toxicol ; 15(4): 187-96, 2001.
Article in English | MEDLINE | ID: mdl-11673847

ABSTRACT

The aryl hydrocarbon receptor (AhR) is a ligand-dependent transcription factor that mediates many of the biological and toxicological actions of a diverse range of chemicals, including the environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, dioxin). Although no endogenous physiological ligand for the AhR has yet been described, numerous studies support the existence of such a ligand(s). Here we have examined the ability of prostaglandins and related chemicals to activate the AhR signaling system. Using two AhR-based bioassay systems we report that relatively high concentrations of several prostaglandins (namely, PGB3, PGD3, PGF3alpha, PGG2, PGH1, and PGH2) can not only stimulate AhR transformation and DNA binding in vitro, but also induce AhR-dependent reporter gene expression in mouse hepatoma cells in culture. PGG2 also induced AhR-dependent reporter gene expression to a level three-to four fold greater than that observed with a maximal inducing dose of TCDD. Sucrose gradient ligand binding analysis revealed that PGG2 could competitively displace [3H]TCDD from the AhR. Overall, our results demonstrate that selected prostaglandins are weak agonists for the AhR and they represent a structurally distinct and novel class of activator of the AhR signal transduction pathway.


Subject(s)
Prostaglandins/pharmacology , Receptors, Aryl Hydrocarbon/drug effects , Signal Transduction/drug effects , Animals , Cells, Cultured , Centrifugation, Density Gradient , Chromatography, Gel , Cytosol/metabolism , DNA/biosynthesis , DNA/genetics , Dinoprostone/pharmacology , Dose-Response Relationship, Drug , Guinea Pigs , Liver/drug effects , Liver/metabolism , Luciferases/metabolism , Male , Mice , Polychlorinated Dibenzodioxins/pharmacology , Receptors, Aryl Hydrocarbon/genetics , Signal Transduction/genetics , Sucrose
2.
Toxicol Sci ; 54(1): 183-93, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10746945

ABSTRACT

Polycyclic and halogenated aromatic hydrocarbons (PAHs/HAHs) are a diverse group of widespread and persistent environmental contaminants that can cause a variety of detrimental effects in vertebrates. As most available methods to detect these contaminants are expensive, labor and time intensive, and require large amounts of tissue for extraction and analysis, several rapid mechanistically based bioassay systems have been developed to detect these chemicals. Here we describe application and optimization of a recently developed recombinant mouse cell bioassay system that responds to both PAHs and HAHs with the rapid induction of firefly luciferase for the detection of these chemicals in whole serum samples. This chemically activated luciferase expression (CALUX) bioassay has been modified to allow rapid (4-h) and direct analysis of small volumes (25-50 microl) of whole serum in a 96-well microtiter plate format without the need for solvent extraction. This bioassay can detect as little as 10 parts per trillion of the most potent HAH, 2,3,7,8-TCDD, and is also sensitive to other HAHs and PAHs. The use of simple procedures corrects for interplate and intraplate variability and the Ah receptor dependence of the induction response is accounted for by use of the antagonist 4-amino-3-methoxyflavone.


Subject(s)
Hydrocarbons, Aromatic/toxicity , Hydrocarbons, Halogenated/toxicity , Polycyclic Aromatic Hydrocarbons/toxicity , Algorithms , Animals , Biological Assay , Cell Line , Clone Cells , Liver Neoplasms, Experimental/metabolism , Luciferases/biosynthesis , Mice
3.
Environ Pollut ; 107(3): 295-304, 2000 Mar.
Article in English | MEDLINE | ID: mdl-15092975

ABSTRACT

The Unocal-Metrolink oil spill of 21 February 1995 resulted in approximately 7800 barrels of San Joaquin crude oil being deposited into the San Gabriel River in Huntington Beach, CA, USA. In order to determine long-term pathological effects of oil exposure and rehabilitation, hematological and serum biochemical parameters for both rehabilitated (RHB) American coots (Fulica americana) and reference (REF) coots were examined every 3-4 weeks (56, 81, 108 and 140 days post oil exposure) after birds were cleaned, rehabilitated and soft-released. Most significant differences in monthly comparisons between RHB and REF birds occurred 56 days following oil exposure. Total white blood cell (WBC) count, albumin:globulin (A:G) ratio and calcium concentration were higher in RHB birds compared to REF birds 56 days post oil exposure. In addition, mean cell hemoglobin (MCH), mean cell hemoglobin concentration (MCHC), alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase and creatine kinase activities, and creatinine, total protein (TP) and globulin concentrations were lower in RHB birds. Blood results from 56 days post oil exposure for RHB coots which subsequently died were compared to blood results from days 108 and 140 for REF coots which survived. Oiled and rehabilitated birds which died had significantly higher WBCs, packed cell volume, TP and globulin concentrations, and lower A:G ratio, MCH, MCHC, glucose and sodium concentrations compared to REF birds which survived. Blood result differences detected at 3-4-week intervals between RHB and REF survivors, and differences detected between RHB coots which died and REF coots which survived, suggested that RHB coots developed an inflammatory response (infectious or non-septic) and, concurrently, may have experienced decreased immune responsiveness. Additionally, RHB coots experienced either an iron (Fe) utilization or Fe metabolism problem. These pathophysiological mechanisms were consistent with increased hemosiderin (stored Fe) present in the liver, spleen and kidney of necropsied RHB birds, and may have contributed to RHB coot mortality. When blood parameter differences were examined for their impact on survival time, it was determined that RHB coots had shorter survival times if they had very high cholesterol (> or =449 mg/dl) or chloride (> or =110 MEQ/l) concentrations on day 56 post oil exposure. Interestingly, the lack of differences between RHB and REF coots from day 81 through day 140 suggested that, from a hematologic and clinical chemistry perspective, coots which were oiled, rehabilitated, released and survived at least 3.5 months could not be differentiated from wild (REF) coots. From these findings it appears that blood analysis, coupled with post-release survival data, may help discern reasons for increased mortality of oiled and rehabilitated birds, compared to non-oiled reference birds.

4.
Toxicol Appl Pharmacol ; 152(2): 406-14, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9853009

ABSTRACT

The aryl hydrocarbon receptor (AhR) is a ligand-dependent transcription factor that mediates many of the biological and toxicological actions of a variety of hydrophobic natural and synthetic chemicals, including the environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, dioxin). Induction of CYP1A1 gene expression is one such response that is known to be regulated by the AhR complex. It was recently reported (Ledirac et al., Toxicol. Appl. Pharmacol. 144, 177-182, 1997) that, although carbaryl, a carbamate insecticide, can induce AhR-dependent expression of CYP1A1, it was not an AhR ligand. Since this apparent ligand-independent activation of the AhR is difficult to reconcile given what is known about the mechanism of AhR action, we have examined the ability of carbaryl to stimulate the AhR signaling pathway. Not only was dioxin responsive element-driven luciferase gene expression induced by carbaryl in stably transfected mouse, rat, guinea pig, and human cells, gel retardation analysis revealed that carbaryl stimulated AhR transformation and DNA binding in vitro and in cells in culture. Dose-response experiments revealed that carbaryl was 300,000-fold less potent that the prototypical inducer, TCDD, in both inducing luciferase gene expression and stimulating AhR transformation and DNA binding in vitro, suggesting that carbaryl itself was the inducing agent. The identification of carbaryl as an AhR ligand was demonstrated by its ability to competitively inhibit [3H]-TCDD to the guinea pig hepatic cytosolic AhR. Our results confirm that carbaryl is both a weak AhR ligand and inducer of AhR-dependent gene expression and argue against its proposed ligand-independent mechanism of AhR activation.


Subject(s)
Carbaryl/metabolism , Gene Expression/drug effects , Insecticides/metabolism , Receptors, Aryl Hydrocarbon/metabolism , Animals , Binding, Competitive , Carbaryl/pharmacology , DNA-Binding Proteins/metabolism , Dioxins/pharmacology , Genes, Reporter , Guinea Pigs , Humans , Insecticides/pharmacology , Ligands , Liver Neoplasms/metabolism , Liver Neoplasms/pathology , Male , Mice , Rats , Receptors, Aryl Hydrocarbon/genetics , Tumor Cells, Cultured
5.
J Wildl Dis ; 32(1): 51-6, 1996 Jan.
Article in English | MEDLINE | ID: mdl-8627936

ABSTRACT

Western blots and a kinetic enzyme-linked immunosorbent assay (ELISA) were used to characterize and quantify the prevalence of antibodies to Psoroptes sp. mites in elk (Cervus elaphus) from nine herds in North America. Sera from infested (n = 18) and non-infested (n = 22) elk were used to optimize test methodology and to define cut-off values for negative, suspect, and positive samples. Among 357 samples, 35 (9.8%) of the animals were seropositive, 259 (73%) were negative, and 63 (18%) were suspect. Six of nine herds (67%) contained positive animals and two additional herds (22%) had suspect animals. Sex was not associated with prevalence of antibodies, but adults greater than 2 yr old were approximately five times more likely (95% confidence interval = 2.6-15.4) to be seropositive than calves. Based on these results, we propose that exposure to Psoroptes sp. mites may be widespread in free-ranging elk of North America.


Subject(s)
Antibodies/blood , Deer/parasitology , Enzyme-Linked Immunosorbent Assay/veterinary , Mite Infestations/veterinary , Mites/immunology , Animals , Blotting, Western/veterinary , Female , Kinetics , Male , Mite Infestations/epidemiology , Odds Ratio , Prevalence , United States/epidemiology
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