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1.
J Appl Toxicol ; 36(6): 863-71, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26857037

RESUMEN

The present study was conducted to assess the effects of Cd exposure on estrogen signaling in the zebrafish brain, as well as the potential protective role of Zn against Cd-induced toxicity. For this purpose, the effects on transcriptional activation of the estrogen receptors (ERs), aromatase B (Aro-B) protein expression and molecular expression of related genes were examined in vivo using wild-type and transgenic zebrafish embryos. For in vitro studies, an ER-negative glial cell line (U251MG) transfected with different zebrafish ER subtypes (ERα, ERß1 and ERß2) was also used. Embryos were exposed either to estradiol (E2 ), Cd, E2 +Cd or E2 +Cd+Zn for 72 h and cells were exposed to the same treatments for 30 h. Our results show that E2 treatment promoted the transcriptional activation of ERs and increased Aro-B expression, at both the protein and mRNA levels. Although exposure to Cd, does not affect the studied parameters when administered alone, it significantly abolished the E2 -stimulated transcriptional response of the reporter gene for the three ER subtypes in U251-MG cells, and clearly inhibited the E2 induction of Aro-B in radial glial cells of zebrafish embryos. These inhibitory effects were accompanied by a significant downregulation of the expression of esr1, esr2a, esr2b and cyp19a1b genes compared to the E2 -treated group used as a positive control. Zn administration during simultaneous exposure to E2 and Cd strongly stimulated zebrafish ERs transactivation and increased Aro-B protein expression, whereas mRNA levels of the three ERs as well as the cyp19a1b remained unchanged in comparison with Cd-treated embryos. In conclusion, our results clearly demonstrate that Cd acts as a potent anti-estrogen in vivo and in vitro, and that Cd-induced E2 antagonism can be reversed, at the protein level, by Zn supplement. Copyright © 2016 John Wiley & Sons, Ltd.


Asunto(s)
Encéfalo/efectos de los fármacos , Intoxicación por Cadmio/prevención & control , Cadmio/toxicidad , Embrión no Mamífero/efectos de los fármacos , Contaminantes Químicos del Agua/toxicidad , Pez Cebra , Zinc/uso terapéutico , Animales , Animales Modificados Genéticamente , Aromatasa/genética , Aromatasa/metabolismo , Encéfalo/metabolismo , Encéfalo/patología , Cadmio/química , Intoxicación por Cadmio/embriología , Intoxicación por Cadmio/metabolismo , Intoxicación por Cadmio/veterinaria , Línea Celular , Embrión no Mamífero/metabolismo , Embrión no Mamífero/patología , Antagonistas de Estrógenos/química , Antagonistas de Estrógenos/toxicidad , Estrógenos/agonistas , Estrógenos/química , Estrógenos/metabolismo , Enfermedades de los Peces/embriología , Enfermedades de los Peces/metabolismo , Enfermedades de los Peces/patología , Enfermedades de los Peces/prevención & control , Regulación del Desarrollo de la Expresión Génica/efectos de los fármacos , Genes Reporteros/efectos de los fármacos , Humanos , Neuroglía/efectos de los fármacos , Neuroglía/metabolismo , Neuroglía/patología , Receptores de Estrógenos/antagonistas & inhibidores , Receptores de Estrógenos/química , Receptores de Estrógenos/genética , Receptores de Estrógenos/metabolismo , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Transducción de Señal/efectos de los fármacos , Contaminantes Químicos del Agua/antagonistas & inhibidores , Pez Cebra/embriología , Pez Cebra/genética , Pez Cebra/metabolismo , Proteínas de Pez Cebra/agonistas , Proteínas de Pez Cebra/antagonistas & inhibidores , Proteínas de Pez Cebra/genética , Proteínas de Pez Cebra/metabolismo , Cigoto/efectos de los fármacos , Cigoto/metabolismo , Cigoto/patología
2.
J Comp Neurol ; 462(2): 180-93, 2003 Jul 21.
Artículo en Inglés | MEDLINE | ID: mdl-12794742

RESUMEN

Recent data indicate that estrogens locally produced in the brain by aromatization of androgens could be important for neurogenesis and brain repair. In this respect, fish are interesting because of the extremely high aromatase activity of their brain. In this study, the rainbow trout brain aromatase was cloned and riboprobes were used to map the distribution of cells expressing the corresponding mRNAs. A very strong hybridization signal was detected in the pituitary and in cells bordering the ventricles in the telencephalon and ventral diencephalon, with the highest expression in the preoptic area and hypothalamus. A weaker signal was detected in the ependymal layer bordering the torus semicircularis and optic tectum. This localization was fully confirmed by immunohistochemistry using antibodies against a teleost aromatase. In addition, this antibody showed that aromatase expression in fact corresponds to radial glial cells because immunoreactive cells had long cytoplasmic processes extending toward the pial surface. Because brain aromatase was shown to be upregulated by estradiol in fish, the distribution of aromatase mRNAs was compared with that of rainbow trout estrogen receptor alpha (rtERalpha) on adjacent sections. Although the highest aromatase expression was found in regions expressing rtERalpha, no obvious coexpression was found, as rtERalpha was never observed in radial cells. However, reverse transcriptase-polymerase chain reaction experiments performed on brain cell cultures enriched in glial cells suggest that a weak expression of rtERalpha in glial cells cannot be excluded. The possible role of the high brain aromatase content in fish could be related to the continuous growth of their central nervous system during adulthood.


Asunto(s)
Aromatasa/genética , Oncorhynchus mykiss/fisiología , Hipófisis/química , Hipófisis/enzimología , Receptores de Estrógenos/genética , Animales , Aromatasa/análisis , Astrocitos/química , Astrocitos/citología , Astrocitos/enzimología , Células Cultivadas , Clonación Molecular , ADN Complementario , Receptor alfa de Estrógeno , Femenino , Regulación Enzimológica de la Expresión Génica , Inmunohistoquímica , Hibridación in Situ , Neuronas/química , Neuronas/citología , Neuronas/enzimología , Hipófisis/citología , ARN Mensajero/análisis , Receptores de Estrógenos/análisis
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