RESUMEN
Young adult wild-type and aryl hydrocarbon receptor knockout (AHRKO) mice of both sexes and the C57BL/6J background were exposed to 10 weekly oral doses of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD; total dose of 200 µg/kg bw) to further characterize the observed impacts of AHR as well as TCDD on the retinoid system. Unexposed AHRKO mice harboured heavier kidneys, lighter livers and lower serum all-trans retinoic acid (ATRA) and retinol (REOH) concentrations than wild-type mice. Results from the present study also point to a role for the murine AHR in the control of circulating REOH and ATRA concentrations. In wild-type mice, TCDD elevated liver weight and reduced thymus weight, and drastically reduced the hepatic concentrations of 9-cis-4-oxo-13,14-dihydro-retinoic acid (CORA) and retinyl palmitate (REPA). In female wild-type mice, TCDD increased the hepatic concentration of ATRA as well as the renal and circulating REOH concentrations. Renal CORA concentrations were substantially diminished in wild-type male mice exclusively following TCDD-exposure, with a similar tendency in serum. In contrast, TCDD did not affect any of these toxicity or retinoid system parameters in AHRKO mice. Finally, a distinct sex difference occurred in kidney concentrations of all the analysed retinoid forms. Together, these results strengthen the evidence of a mandatory role of AHR in TCDD-induced retinoid disruption, and suggest that the previously reported accumulation of several retinoid forms in the liver of AHRKO mice is a line-specific phenomenon. Our data further support participation of AHR in the control of liver and kidney development in mice.
Asunto(s)
Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/metabolismo , Contaminantes Ambientales/toxicidad , Dibenzodioxinas Policloradas/toxicidad , Receptores de Hidrocarburo de Aril/metabolismo , Retinoides/metabolismo , Animales , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Peso Corporal , Femenino , Riñón/efectos de los fármacos , Riñón/crecimiento & desarrollo , Riñón/metabolismo , Hígado/efectos de los fármacos , Hígado/crecimiento & desarrollo , Hígado/metabolismo , Masculino , Ratones Endogámicos C57BL , Ratones Noqueados , Tamaño de los Órganos , Receptores de Hidrocarburo de Aril/genética , Retinoides/sangre , Caracteres Sexuales , Testículo/efectos de los fármacos , Testículo/crecimiento & desarrollo , Timo/efectos de los fármacos , Timo/crecimiento & desarrolloRESUMEN
In rats, direct exposure to TCDD causes myriad toxicities. Exposed rats experience hepatotoxicity, wasting syndrome and immune suppression, amongst others. "Inherited exposure", as occurs in the F3 generation of directly exposed F0 animals, has also been shown to cause toxicity: both male and female F3 rats demonstrate an increased incidence of adult onset disease, females also display reproductive abnormalities and increased incidence of ovarian diseases while males show increased incidence of kidney disease and an altered sperm epigenome. Here, we explore the hepatic transcriptomic profile of male and female F3 Sprague-Dawley rats bred through the paternal germ line from F0 dams exposed to a single dose of TCDD (0, 30, 100, 300 or 1000 ng/kg body weight) by oral gavage. We hypothesize that RNA transcripts with altered abundance in livers of unexposed F3 progeny of treated F0 Sprague-Dawley rats may result from epigenetic modifications to the genome. We further survey patterns of differential methylation within male F3 rat testis. Female F3 rats demonstrated more TCDD-mediated hepatic transcriptomic changes than males, with differences primarily in the lowest dose group. In testis from male F3 rats, multiple olfactory receptors displayed patterns of differential methylation. Hypermethylation of Egfr and Mc5r among testes from TCDD lineage rats was observed, but without corresponding changes in hepatic mRNA abundance. Further studies examining these differences in other tissue types are warranted.
Asunto(s)
Contaminantes Ambientales/toxicidad , Dibenzodioxinas Policloradas/toxicidad , Animales , Peso Corporal , Metilación de ADN , Epigénesis Genética , Femenino , Genoma , Enfermedades Renales , Masculino , Ratas , Ratas Sprague-Dawley , Espermatozoides , Testículo , TranscriptomaRESUMEN
In a previous study of female Han/Wistar (H/W) and Long-Evans (L-E) rats, we found that adult exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) was associated with size decreases in the cranium and especially the face. In this study we compared these crania to those from male and female Sprague-Dawley (S-D) rats with in utero/lactational exposure to TCDD, using morphometric variables of size, shape, and fluctuating asymmetry to quantify the effects of dose on craniofacial development and growth. At the highest levels of exposure, in utero/lactational and adult TCDD exposures both resulted in small but significant reductions in facial size parameters (i.e., 3-5%) in only females and minor effects on facial shape in both sexes. The shape effects of in utero/lactational exposure were most significant at the sutural intersections, whereas adult exposure to TCDD corresponded to dose-dependent changes of decreasing facial length and vault breadth. Fluctuating asymmetry in general explained a relatively small amount of shape variation compared with other effects, and only increased significantly in female L-E rats with high levels of adult exposure to TCDD. These results indicate that TCDD-related changes in cranial development and growth in rats can vary with the timing and duration of exposure, and with sex. Further investigations of other dioxin-like compounds and animal species will broaden our understanding of how chemicals exposure can influence the development and growth of the mammalian skeleton.
Asunto(s)
Anomalías Craneofaciales/patología , Contaminantes Ambientales/toxicidad , Lactancia , Dibenzodioxinas Policloradas/toxicidad , Tejido Adiposo/metabolismo , Envejecimiento , Animales , Anomalías Craneofaciales/inducido químicamente , Relación Dosis-Respuesta a Droga , Contaminantes Ambientales/farmacocinética , Femenino , Metabolismo de los Lípidos/efectos de los fármacos , Masculino , Dibenzodioxinas Policloradas/farmacocinética , Embarazo , Efectos Tardíos de la Exposición Prenatal/patología , Ratas , Ratas Long-Evans , Ratas Sprague-Dawley , Ratas WistarRESUMEN
PCB 180 is a persistent non-dioxin-like polychlorinated biphenyl (NDL-PCB) abundantly present in food and the environment. Risk characterization of NDL-PCBs is confounded by the presence of highly potent dioxin-like impurities. We used ultrapure PCB 180 to characterize its toxicity profile in a 28-day repeat dose toxicity study in young adult rats extended to cover endocrine and behavioral effects. Using a loading dose/maintenance dose regimen, groups of 5 males and 5 females were given total doses of 0, 3, 10, 30, 100, 300, 1000 or 1700 mg PCB 180/kg body weight by gavage. Dose-responses were analyzed using benchmark dose modeling based on dose and adipose tissue PCB concentrations. Body weight gain was retarded at 1700 mg/kg during loading dosing, but recovered thereafter. The most sensitive endpoint of toxicity that was used for risk characterization was altered open field behavior in females; i.e. increased activity and distance moved in the inner zone of an open field suggesting altered emotional responses to unfamiliar environment and impaired behavioral inhibition. Other dose-dependent changes included decreased serum thyroid hormones with associated histopathological changes, altered tissue retinoid levels, decreased hematocrit and hemoglobin, decreased follicle stimulating hormone and luteinizing hormone levels in males and increased expression of DNA damage markers in liver of females. Dose-dependent hypertrophy of zona fasciculata cells was observed in adrenals suggesting activation of cortex. There were gender differences in sensitivity and toxicity profiles were partly different in males and females. PCB 180 adipose tissue concentrations were clearly above the general human population levels, but close to the levels in highly exposed populations. The results demonstrate a distinct toxicological profile of PCB 180 with lack of dioxin-like properties required for assignment of WHO toxic equivalency factor. However, PCB 180 shares several toxicological targets with dioxin-like compounds emphasizing the potential for interactions.
Asunto(s)
Conducta Animal/efectos de los fármacos , Contaminantes Ambientales/toxicidad , Conducta Exploratoria/efectos de los fármacos , Bifenilos Policlorados/toxicidad , Tejido Adiposo/efectos de los fármacos , Corteza Suprarrenal/efectos de los fármacos , Animales , Peso Corporal/efectos de los fármacos , Daño del ADN , Relación Dosis-Respuesta a Droga , Contaminantes Ambientales/farmacocinética , Femenino , Hormona Folículo Estimulante/metabolismo , Hematócrito , Hemoglobinas/metabolismo , Hígado/efectos de los fármacos , Hígado/metabolismo , Hormona Luteinizante/metabolismo , Masculino , Bifenilos Policlorados/farmacocinética , Ratas , Ratas Sprague-Dawley , Retinoides/metabolismo , Factores Sexuales , Hormonas Tiroideas/sangreRESUMEN
Bone is a target for high affinity aryl hydrocarbon receptor (AHR) ligands, such as dioxins. Although bone morphology, mineral density and strength are sensitive endpoints of dioxin toxicity, less is known about effects on bone microarchitecture and material properties. This study characterizes TCDD-induced modulations of bone tissue, and the role of AHR in dioxin-induced bone toxicity and for normal bone phenotype. Six AHR-knockout (Ahr(-/-)) and wild-type (Ahr(+/+)) mice of both genders were exposed to TCDD weekly for 10 weeks, at a total dose of 200µg/kgbw. Bones were examined with micro-computed tomography, nanoindentation and biomechanical testing. Serum levels of bone remodeling markers were analyzed, and the expression of genes related to osteogenic differentiation was profiled using PCR array. In Ahr(+/+) mice, TCDD-exposure resulted in harder bone matrix, thinner and more porous cortical bone, and a more compact trabecular bone compartment. Bone remodeling markers and altered expression of a number of osteogenesis related genes indicated imbalanced bone remodeling. Untreated Ahr(-/-) mice displayed a slightly modified bone phenotype as compared with untreated Ahr(+/+) mice, while TCDD exposure caused only a few changes in bones of Ahr(-/-) mice. Part of the effects of both TCDD-exposure and AHR-deficiency were gender dependent. In conclusion, exposure of adult mice to TCDD resulted in harder bone matrix, thinner cortical bone, mechanically weaker bones and most notably, increased trabecular bone volume fraction in Ahr(+/+) mice. AHR is involved in bone development of a normal bone phenotype, and is crucial for manifestation of TCDD-induced bone alterations.
Asunto(s)
Remodelación Ósea/efectos de los fármacos , Huesos/efectos de los fármacos , Dibenzodioxinas Policloradas/toxicidad , Receptores de Hidrocarburo de Aril/metabolismo , Animales , Biomarcadores/sangre , Peso Corporal/efectos de los fármacos , Huesos/metabolismo , Colágeno Tipo I/sangre , Colágeno Tipo II/genética , Colágeno Tipo II/metabolismo , Colágeno Tipo X/genética , Colágeno Tipo X/metabolismo , Femenino , Regulación de la Expresión Génica , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Osteogénesis/genética , Fragmentos de Péptidos/sangre , Fenotipo , Procolágeno/sangre , Factores de Empalme de ARN , Proteínas de Unión al ARN , Receptores de Hidrocarburo de Aril/genética , Factor B de Crecimiento Endotelial Vascular/genética , Factor B de Crecimiento Endotelial Vascular/metabolismo , Proteínas de Transporte Vesicular/genética , Proteínas de Transporte Vesicular/metabolismo , alfa-2-Glicoproteína-HS/genética , alfa-2-Glicoproteína-HS/metabolismoRESUMEN
Dioxins are known to decrease bone strength, architecture and density. However, their detailed effects on bone material properties are unknown. Here we used nanoindentation methods to characterize the effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on nanomechanical behaviour of bone matrix. Pregnant rats were treated with a single intragastric dose of TCDD (1 microg/kg) or vehicle on gestational day 11. Tibias of female offspring were sampled on postnatal day (PND) 35 or 70, scanned at mid-diaphysis with pQCT, and evaluated by three-point bending and nanoindentation. TCDD treatment decreased bone mineralization (p<0.05), tibial length (p<0.01), cross-sectional geometry (p<0.05) and bending strength (p<0.05). Controls showed normal maturation pattern between PND 35 and 70 with decreased plasticity by 5.3% and increased dynamic hardness, storage and complex moduli by 26%, 13% and 12% respectively (p<0.05), while similar maturation was not observed in TCDD-exposed pups. In conclusion, for the first time, we demonstrate retardation of bone matrix maturation process in TCDD-exposed animals. In addition, the study confirms that developmental TCDD exposure has adverse effects on bone size, strength and mineralization. The current results in conjunction with macromechanical behaviour suggest that reduced bone strength caused by TCDD is more associated with the mineralization and altered geometry of bones than with changes at the bone matrix level.
Asunto(s)
Matriz Ósea/efectos de los fármacos , Matriz Ósea/fisiopatología , Dibenzodioxinas Policloradas/toxicidad , Animales , Fenómenos Biomecánicos , Densidad Ósea/efectos de los fármacos , Matriz Ósea/patología , Femenino , Nanotecnología , Dibenzodioxinas Policloradas/administración & dosificación , Embarazo , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Efectos Tardíos de la Exposición Prenatal/patología , Efectos Tardíos de la Exposición Prenatal/fisiopatología , Ratas , Ratas Sprague-Dawley , Estrés Mecánico , Tibia/efectos de los fármacos , Tibia/patología , Tibia/fisiopatologíaRESUMEN
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD), the model compound of polychlorinated dibenzo-p-dioxins and furans, is a potent toxicant with the ability to hamper development. Accidental exposure to TCDD has been linked with various developmental dental aberrations in humans, and experimentally it has been shown that TCDD causes, among other defects, hypomineralization of dental hard tissues in rodents. Here, we studied the effect of very low perinatal TCDD exposure on dental caries susceptibility and mineral composition of tooth enamel in rats. Pregnant line C rats (rat line developed in our laboratory) were dosed 0.03-1.0 microg/kg TCDD on gestation day 15 and allowed to give birth and nurse until weaning on postnatal day 21. The offspring were challenged with cariogenic treatment including sugar-rich diet and three inoculations with Streptococcus mutans. Control groups involved animals with or without cariogenic challenge or TCDD treatment. The number of caries lesions in left lower molars was determined by Schiff's staining after 8 weeks of weaning. TCDD treatment increased cariogenic lesions in the enamel at the lowest maternal dose used, 0.03 microg/kg, and at the highest maternal dose, 1 microg/kg, the lesions extended through the enamel to dentin more frequently. Changes in mineral composition measured by electron probe microanalyzer, scanning electron microscopy, and energy-dispersive spectrometry could not explain the increased caries susceptibility. In conclusion, perinatal TCDD exposure can render rat molars more susceptible to caries.
Asunto(s)
Susceptibilidad a Enfermedades/inducido químicamente , Diente Molar/efectos de los fármacos , Dibenzodioxinas Policloradas/toxicidad , Efectos Tardíos de la Exposición Prenatal , Anomalías Inducidas por Medicamentos , Animales , Caries Dental , Esmalte Dental/química , Dentina/química , Dieta Cariógena , Contaminantes Ambientales/toxicidad , Femenino , Masculino , Minerales/análisis , Diente Molar/anomalías , Embarazo , Ratas , Ratas EndogámicasRESUMEN
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is a notorious model compound of highly toxic environmental pollutants, polychlorinated dibenzo-p-dioxins (PCDDs). Their toxic effects are mediated via cytosolic aryl hydrocarbon receptor (AHR). We studied the effects of several dose levels of TCDD on developing rat bone after maternal exposure at different times of gestation and lactation in three differentially sensitive rat lines. Rat lines A, B, and C differ in their sensitivity to TCDD due to mutated AHR (Ahr(hw)) in line A and another TCDD-resistance allele (B(hw)) in line B. Line C rats have no resistance alleles. Offspring were analyzed for bone mineral density and geometry by peripheral quantitative computed tomography (pQCT) and for bone biomechanics by three-point bending at mid-diaphysis of tibia and femur and by axial loading at femoral neck. TCDD treatment resulted in bone defects, mainly in offspring of the most sensitive line C at a maternal dose of 1 microg/kg. They included decreased bone length, cross-sectional area of cortex, and bone mineral density. Mechanical testing revealed significantly reduced bending breaking force and stiffness of tibia, femur, and femoral neck. The effects were exposure time-dependent, and earlier exposure caused more severe defects. Gestational exposure alone was not sufficient, but lactational exposure was required to cause the bone defects. Most of the defects were recovered at the age of 1 year. The results indicate that dioxins affect developing bone by interfering with bone growth and mechanical strength and that the effects are mainly reversible. The dioxin-resistance alleles, Ahr(hw) and B(hw) increase the resistance to these defects.
Asunto(s)
Desarrollo Óseo/efectos de los fármacos , Contaminantes Ambientales/toxicidad , Lactancia/fisiología , Dibenzodioxinas Policloradas/toxicidad , Alelos , Animales , Animales Recién Nacidos , Fenómenos Biomecánicos , Peso Corporal/efectos de los fármacos , Densidad Ósea/efectos de los fármacos , Línea Celular , Densitometría , Relación Dosis-Respuesta a Droga , Contaminantes Ambientales/farmacocinética , Femenino , Desarrollo Fetal , Masculino , Tamaño de los Órganos/efectos de los fármacos , Dibenzodioxinas Policloradas/administración & dosificación , Dibenzodioxinas Policloradas/farmacocinética , Embarazo , Efectos Tardíos de la Exposición Prenatal , Ratas , Receptores de Hidrocarburo de Aril/genética , Caracteres Sexuales , SobrevidaRESUMEN
The contribution of genetic factors to adult male reproductive system toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) was analyzed in three rat lines differentially resistant to TCDD acute lethality: line A, B, and C rats (selectively bred from TCDD-resistant Han/Wistar [Kuopio; H/W] and TCDD-sensitive Long-Evans [Turku/AB; L-E] rats). The resistance is linked to a mutated H/W-type aryl hydrocarbon receptor allele in line A and to an H/W-type unknown "B" allele in line B. Line C rats do not have resistance alleles. Mature male line A, B and C rats were given single oral doses up to 1000, 300, and 30 micrograms/kg TCDD, respectively. The dose-responses of TCDD effects on male reproductive organ weights, sperm numbers, and serum testosterone concentrations were analyzed 17 days after exposure. Serum testosterone concentrations were decreased by the highest doses of TCDD, and there were no major sensitivity differences among the rat lines. Correspondingly, the decrease in relative weight of ventral prostate and seminal vesicles was seen only after a dose of >/=100 micrograms/kg TCDD. Thus the effect was observed only in resistant lines A and B. The relative weights of testes and epididymides were not affected. Significant decrease in spermatogenesis was observed in each rat line, but the amount of decrease was reduced by resistance alleles. The highest TCDD dose decreased the daily sperm production by 37, 38, and 60% in line A, B, and C rats, respectively. Therefore, the resistance alleles appear to selectively modify the TCDD effects on the adult male reproductive system. The fact that the influence of resistance alleles on spermatogenesis is different from that on androgenic status indicates that the effect of TCDD on sperm numbers is not fully related to decreased serum testosterone.
Asunto(s)
Contaminantes Ambientales/toxicidad , Genitales Masculinos/efectos de los fármacos , Dibenzodioxinas Policloradas/toxicidad , Alelos , Animales , Peso Corporal/efectos de los fármacos , Epidídimo/citología , Genitales Masculinos/patología , Masculino , Tamaño de los Órganos/efectos de los fármacos , Ratas , Ratas Long-Evans , Ratas Wistar , Receptores de Hidrocarburo de Aril/genética , Vesículas Seminales/efectos de los fármacos , Células de Sertoli/efectos de los fármacos , Recuento de Espermatozoides , Cabeza del Espermatozoide/efectos de los fármacos , Espermatogénesis/efectos de los fármacos , Testículo/patología , Testosterona/sangreRESUMEN
Dioxins are persistent environmental contaminants that cause multiple disorders in laboratory animals, including teratogenesis. In mice, the most important teratogenic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) are hydronephrosis and cleft palate. Aryl hydrocarbon receptor (AHR) mediates most of the TCDD-induced effects, but modulation of these effects by other factors such as epidermal growth factor receptor (EGFR) has been propounded. TCDD changes the expression of both EGF and its receptor EGFR, which may be one step in the pathway leading to cleft palate and hydronephrosis. In the present study, the importance of EGFR in TCDD-induced teratogenicity was evaluated. Heterozygous EGFR(+/-)-mice were mated and pregnant females exposed to 1.5-106.0 microg/kg TCDD on gestation day (GD) 10 and killed on GD 18. The fetuses were studied for cleft palate, hydronephrosis, and open eyes. There was no marked difference among the three genotypes in sensitivity to cleft palate or hydronephrosis, but in EGFR(-/-)-mice frequency of the open eye malformation decreased dose-dependently. In conclusion, EGFR signaling is not required for TCDD-induced cleft palate or hydronephrosis but TCDD appears to counteract the effect of EGFR deficiency on eye opening.
Asunto(s)
Receptores ErbB/deficiencia , Desarrollo Fetal/efectos de los fármacos , Dibenzodioxinas Policloradas/toxicidad , Efectos Tardíos de la Exposición Prenatal , Teratógenos/toxicidad , Animales , Fisura del Paladar/embriología , Fisura del Paladar/etiología , Relación Dosis-Respuesta a Droga , Receptores ErbB/genética , Anomalías del Ojo/embriología , Anomalías del Ojo/etiología , Femenino , Desarrollo Fetal/genética , Genotipo , Hidronefrosis/embriología , Hidronefrosis/etiología , Masculino , Ratones , Ratones Noqueados , Diente Molar/efectos de los fármacos , Diente Molar/embriología , EmbarazoRESUMEN
We have previously shown that tooth development is a sensitive endpoint of dioxin toxicity. In the present study we determined the critical window of sensitivity for 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced toxicity for the development of rat molar teeth. Dams were exposed to 1 microg/kg once over a time range covering the development of each molar tooth. A cross-fostering study also was conducted. Pups were killed at the age of 40 days. Erupted molars were observed by stereomicroscopy. The jaws were radiographed, the presence of molars assessed from the radiographs, and the molars measured. Pups exposed both in utero and via lactation lacked third molars and the frequency of missing molars was greater the earlier the dam was exposed: 100, 88, and 50% of the offspring exposed on gestation day (GD) 11, GD13, and GD19, respectively. All third molars developed in offspring of dams exposed on postnatal day (PND) 0, PND2, or PND4. None of the exposed pups lacked the first or the second molars. In the cross-foster study, 32 and 4% of offspring exposed only in utero and only via lactation, respectively, lacked molars. TCDD accelerated the eruption of the lower incisors and retarded the eruption of the third molars. The most critical window of sensitivity for the development of the third molar was during the early morphogenesis, from tooth initiation to the early bud stage, after which the sensitivity substantially decreased. Response to TCDD was increased if the exposure was started several days before this critical window of sensitivity or if it was continued thereafter. Dental epithelium is the likely target of TCDD.