1996
DOI: 10.1016/s0166-445x(96)00799-0
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Estrogenic activity of chlordecone, o,p′-DDT and o,p′-DDE in juvenile rainbow trout: induction of vitellogenesis and interaction with hepatic estrogen binding sites

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Cited by 162 publications
(109 citation statements)
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“…Concentrations of individual contaminants and mixtures determined in this study have been shown to have adverse effects in a wide range of animals, including mammals, reptiles, amphibians, and fish (20)(21)(22)(23). Some of the effects described are as follows: alterations of growth and development (24), poor hatching success (22), alterations of the reproductive and nervous system (25,26), learning and behavioral deficits retained throughout life (27,28), abnormalities of the liver and other organ systems (29,30), and endocrine disruption (29,31). Studies have also shown that these contaminants in combination can increase adverse effects by several orders of magnitude (32,33).…”
Section: Discussionmentioning
confidence: 99%
“…Concentrations of individual contaminants and mixtures determined in this study have been shown to have adverse effects in a wide range of animals, including mammals, reptiles, amphibians, and fish (20)(21)(22)(23). Some of the effects described are as follows: alterations of growth and development (24), poor hatching success (22), alterations of the reproductive and nervous system (25,26), learning and behavioral deficits retained throughout life (27,28), abnormalities of the liver and other organ systems (29,30), and endocrine disruption (29,31). Studies have also shown that these contaminants in combination can increase adverse effects by several orders of magnitude (32,33).…”
Section: Discussionmentioning
confidence: 99%
“…Although estrogens at this concentration can cause sex reversal (Papoulias et al 1999), the comparatively lower affinity of o,p´-DDE and o,p´-DDT for the ER (Nimrod and Benson 1997) suggests that higher exposures of these compounds are required for sex reversal to occur. Nevertheless, o,p´-DDT and o,p´-DDE at low concentrations may interfere with the binding of natural ligands to a variety of steroid binding moieties (e.g., receptors and binding proteins) (Danzo 1997;Donohoe and Curtis 1996;Gaido et al 1997;Kupfer and Bulger 1976;Lundholm 1998;Mason and Schulte 1980;Nimrod and Benson 1997;Shilling and Williams 2000;Wells and Van Der Kraak 2000), thereby allowing for endocrine-disrupting effects.…”
Section: Discussionmentioning
confidence: 99%
“…However, like o,p´-DDT, o,p´-DDE is believed to work through the ER and to have a similar ER agonist potency (Donohoe and Curtis 1996), and exposure to o,p´-DDE has been associated with decreased fecundity and fertility and increased early oocyte atresia (Hose et al 1989). Recently, Wells and Van Der Kraak (2000) showed that o,p´-DDE and o,p´-DDT will also bind to the androgen receptor in goldfish (Carassius auratus) but not rainbow trout (Oncorhynchus mykiss) testes at approximately half the affinity of p,p´-DDE.…”
mentioning
confidence: 99%
“…The 20-HE disruption corroborates the hypothesis that CLD could be endocrine disruptor in invertebrates as already observed in vertebrates. Indeed, several previous studies have demonstrated that CLD could be an endocrine disruptor in vertebrates such as fish (Ankley et al, 1998;Donohoe and Curtis, 1996;Nimrod and Benson, 1997;Sumpter and Jobling, 1995), birds and mammals (Eroschenko, 1981), by having estrogenic properties through interaction with the estrogen-receptor system (Donohoe and Curtis, 1996;Hammond et al, 1979;Rodríguez et al, 2007). In crustaceans, various estrogenic compounds and estrogen receptor agonists (e.g.…”
Section: Chlordecone Effects On the 20-he Concentrationmentioning
confidence: 99%