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Title: Endocrine disruption mechanism of o,p'-DDT in mature male tilapia (Oreochromis niloticus)

Abstract

The aim of the present study was to evaluate, in vivo, the potential of o,p'-DDT to disrupt the endocrine system of mature male tilapia. In particular, the possibility that o,p'-DDT effects were mediated directly via the estrogen receptor (ER). Compounds with known ability to bind to the ER were employed: estradiol to induce and tamoxifen to inhibit the estrogenic effects result of the activation of the ER. In addition, an aromatase inhibitor, 4-hydrxyandrostenedione (4-OHA), was used to assess the ability of o,p'-DDT to induce estrogenic effects in a surrounding of low estradiol concentration. The effects of estradiol and o,p'-DDT were studied alone or in the presence of tamoxifen or 4-OHA at the end of a 12-day period of exposure. The main endpoints measured were plasma alkaline-labile phosphorous (ALP; an indirect indicator of vitellogenin), estradiol, testosterone and o,p'-DDT. It was found that o,p'-DDT was able to induce the vitellogenesis (measured as plasma ALP increase) and decrease the circulating levels of estradiol and testosterone. Interestingly, o,p'-DDT kept this ability in whole fish with low concentrations of estradiol which would exclude endogenous estradiol as indirect mediator of the estrogenic effects induced by o,p'-DDT. In addition, the plasma concentration of o,p'-DDT, instead of thatmore » of estradiol, was closely related to the plasma ALP increase induced by o,p'-DDT. This indicates that o,p'-DDT could have directly activated the vitellogenesis. The antiestrogenic action of tamoxifen to inhibit the vitellogenesis and the decrease on plasma estradiol induced by o,p'-DDT indicates that o,p'-DDT can bind directly to the ER. In conclusion, this in vivo study shows that o,p'-DDT has the potential to disrupt the endocrine system and strongly supports that the estrogenic actions of o,p'-DDT involve binding to the ER.« less

Authors:
 [1];  [2];  [3];  [3]
  1. Department of Integrative Biology, University of Guelph, Ontario, N1G 2W1 (Canada). E-mail: olgalidia09@yahoo.com
  2. Department of Integrative Biology, University of Guelph, Ontario, N1G 2W1 (Canada)
  3. Departamento de Recursos del Mar, CINVESTAV Unidad Merida, Carretera Antigua a Progreso km. 6, Ap. Postal 73 'Cordemex', Merida, Yucatan 97310 (Mexico)
Publication Date:
OSTI Identifier:
20976944
Resource Type:
Journal Article
Resource Relation:
Journal Name: Toxicology and Applied Pharmacology; Journal Volume: 221; Journal Issue: 2; Other Information: DOI: 10.1016/j.taap.2007.03.011; PII: S0041-008X(07)00108-1; Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; BIOLOGICAL INDICATORS; BLOOD PLASMA; DDT; ERBIUM COMPOUNDS; ESTRADIOL; IN VIVO; RECEPTORS; TAMOXIFEN; TESTOSTERONE

Citation Formats

Leanos-Castaneda, Olga, Kraak, Glen van der, Rodriguez-Canul, Rossanna, and Gold, G. Endocrine disruption mechanism of o,p'-DDT in mature male tilapia (Oreochromis niloticus). United States: N. p., 2007. Web. doi:10.1016/j.taap.2007.03.011.
Leanos-Castaneda, Olga, Kraak, Glen van der, Rodriguez-Canul, Rossanna, & Gold, G. Endocrine disruption mechanism of o,p'-DDT in mature male tilapia (Oreochromis niloticus). United States. doi:10.1016/j.taap.2007.03.011.
Leanos-Castaneda, Olga, Kraak, Glen van der, Rodriguez-Canul, Rossanna, and Gold, G. Fri . "Endocrine disruption mechanism of o,p'-DDT in mature male tilapia (Oreochromis niloticus)". United States. doi:10.1016/j.taap.2007.03.011.
@article{osti_20976944,
title = {Endocrine disruption mechanism of o,p'-DDT in mature male tilapia (Oreochromis niloticus)},
author = {Leanos-Castaneda, Olga and Kraak, Glen van der and Rodriguez-Canul, Rossanna and Gold, G.},
abstractNote = {The aim of the present study was to evaluate, in vivo, the potential of o,p'-DDT to disrupt the endocrine system of mature male tilapia. In particular, the possibility that o,p'-DDT effects were mediated directly via the estrogen receptor (ER). Compounds with known ability to bind to the ER were employed: estradiol to induce and tamoxifen to inhibit the estrogenic effects result of the activation of the ER. In addition, an aromatase inhibitor, 4-hydrxyandrostenedione (4-OHA), was used to assess the ability of o,p'-DDT to induce estrogenic effects in a surrounding of low estradiol concentration. The effects of estradiol and o,p'-DDT were studied alone or in the presence of tamoxifen or 4-OHA at the end of a 12-day period of exposure. The main endpoints measured were plasma alkaline-labile phosphorous (ALP; an indirect indicator of vitellogenin), estradiol, testosterone and o,p'-DDT. It was found that o,p'-DDT was able to induce the vitellogenesis (measured as plasma ALP increase) and decrease the circulating levels of estradiol and testosterone. Interestingly, o,p'-DDT kept this ability in whole fish with low concentrations of estradiol which would exclude endogenous estradiol as indirect mediator of the estrogenic effects induced by o,p'-DDT. In addition, the plasma concentration of o,p'-DDT, instead of that of estradiol, was closely related to the plasma ALP increase induced by o,p'-DDT. This indicates that o,p'-DDT could have directly activated the vitellogenesis. The antiestrogenic action of tamoxifen to inhibit the vitellogenesis and the decrease on plasma estradiol induced by o,p'-DDT indicates that o,p'-DDT can bind directly to the ER. In conclusion, this in vivo study shows that o,p'-DDT has the potential to disrupt the endocrine system and strongly supports that the estrogenic actions of o,p'-DDT involve binding to the ER.},
doi = {10.1016/j.taap.2007.03.011},
journal = {Toxicology and Applied Pharmacology},
number = 2,
volume = 221,
place = {United States},
year = {Fri Jun 01 00:00:00 EDT 2007},
month = {Fri Jun 01 00:00:00 EDT 2007}
}
  • Previous studies indicated that maturation inducing hormone, 17α, 20β-Dihydroxy-4-pregnen-3-one (DHP), probably through nuclear progestin receptor (Pgr), might be involved in spermatogenesis and oogenesis in fish. To further elucidate DHP actions in teleostean ovarian differentiation, we analyzed the expression of pgr in the ovary of Nile tilapia (Oreochromis niloticus), and performed RU486 (a synthetic Pgr antagonist) treatment in XX fish from 5 days after hatching (dah) to 120dah. Tilapia Pgr was abundantly expressed in the follicular cells surrounding oocytes at 30 and 90dah. Continuous RU486 treatment led to the blockage of oogenesis and masculinization of somatic cells in XX fish. Terminationmore » of RU486 treatment and maintenance in normal condition resulted in testicular differentiation, and estrogen compensation in RU486-treated XX fish successfully restored oogenesis. In RU486-treated XX fish, transcript levels of female dominant genes were significantly reduced, while male-biased genes were evidently augmented. Meanwhile, both germ cell mitotic and meiotic markers were substantially reduced. Consistently, estrogen production levels were significantly declined in RU486-treated XX fish. Taken together, our data further proved that DHP, possibly through Pgr, might be essential in the ovarian differentiation and estrogen production in fish. - Highlights: • DHP plays a critical role in early stage oogenesis of XX tilapia. • Blockage of DHP actions by RU486 treatment led to masculinization and/or sex reversal in XX tilapia. • Both DHP and estrogen are indispensable for ovarian differentiation.« less
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  • Pro and antioxidant parameters were compared in the erythrocytes, gill, liver and kidney of Nile Tilapia from a fish farm (Reference group) and from a polluted site at Billings Reservoir (Reservoir group). The erythrocyte oxidative stress was characterized by the increased oxygen uptake and decreased time induction (induced by t-butyl hydroperoxide, t-BHP) evidencing a higher susceptibility to oxidative damage. Moreover, a decrease in both catalase (CAT) activity and total glutathione content (GSH) in erythrocytes of Reservoir fish were observed. The higher gill cytochrome b{sub 5} levels is probably related to the enhanced oxyradical production. This fact associated to the diminishedmore » CAT and G6PDH activities establish a gill oxidative stress of Reservoir fish. The liver pro-oxidant parameters were greatly increased in the Reservoir fish. These results together with the increase in SOD activity and decrease in CAT, glutathione reductase (GR) and G6PDH activities indicate a liver oxidative stress condition. The observed increase in kidney NADH cytochrome c reductase and in both P-450 and b{sub 5} contents did not reflect in enhanced oxyradical production. The decrease in GSH observed in this tissue is probably associated to the conjugation reactions for ulterior excretion. These results furnish useful data for prospections of polluted aquatic sites in order to correlate the presence of pollutants to associated biological effects.« less
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