2010
DOI: 10.1016/j.aquatox.2010.06.009
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17α-Ethinylestradiol disrupts the ontogeny of the forebrain GnRH system and the expression of brain aromatase during early development of zebrafish

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Cited by 81 publications
(45 citation statements)
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“…The increase in fluorescence intensity of GnRH3 neural populations at 3 dpf could also reflect a proliferative action of BPA (Nanjappa et al, 2012) on GnRH3 neurons during early life stages, while the decrease in the fluorescence intensity of GnRH3 neurons at 5 dpf could be the result of an autocrine/ paracrine negative feedback system (Karigo and Oka, 2013) in response to the initial over-expression of GnRH3. Mechanisms underlying BPA-induced bidirectional changes in TN-GnRH3 neurons at the two development time points are not currently known; however, exposure-time sensitive actions of endocrine disrupting chemicals in developing brains have been reported in several studies (Peretz et al, 2014;Ramos et al, 2003;Vosges et al, 2010). For instance, chronic exposure to 17alpha-ethinylestradiol, a potent estrogenic compound, suppressed the size of the GnRH-immunoreactive soma in 10 dpf zebrafish (a closely related teleost) larvae, but not in 5, 20 and 30 dpf larvae (Vosges et al, 2010).…”
Section: Embryonic Bpa Exposure Alters Fluorescence Intensity Of Tngnmentioning
confidence: 98%
“…The increase in fluorescence intensity of GnRH3 neural populations at 3 dpf could also reflect a proliferative action of BPA (Nanjappa et al, 2012) on GnRH3 neurons during early life stages, while the decrease in the fluorescence intensity of GnRH3 neurons at 5 dpf could be the result of an autocrine/ paracrine negative feedback system (Karigo and Oka, 2013) in response to the initial over-expression of GnRH3. Mechanisms underlying BPA-induced bidirectional changes in TN-GnRH3 neurons at the two development time points are not currently known; however, exposure-time sensitive actions of endocrine disrupting chemicals in developing brains have been reported in several studies (Peretz et al, 2014;Ramos et al, 2003;Vosges et al, 2010). For instance, chronic exposure to 17alpha-ethinylestradiol, a potent estrogenic compound, suppressed the size of the GnRH-immunoreactive soma in 10 dpf zebrafish (a closely related teleost) larvae, but not in 5, 20 and 30 dpf larvae (Vosges et al, 2010).…”
Section: Embryonic Bpa Exposure Alters Fluorescence Intensity Of Tngnmentioning
confidence: 98%
“…Studies dedicated to the impacts of EE2 in the brain of fish are very scarse. When larvae are exposed to EE2, the early development of the forebrain GnRH neurons circuitry is impaired with an increase in the number of GnRH neurons, a reduction in the size of their soma and a modification of their migration [134,135]. Taking advantage of the cyp19a1b-GFP transgenic zebrafish line (GFP expression restricted to RGCs and the strong susceptibility of the cyp19a1b promoter to estrogens), it has been shown that EE2 were approximately 50 times more potent than estradiol to induced fluorescence in RGCs of zebrafish larvae treated during 5 days [124].…”
Section: Adverse Effects Of Endocrine Disruptors During Early Neurogementioning
confidence: 99%
“…However, the mechanism of EE 2 in addition to metals on the disruption of HPLG axis is not clear. In this regard, increases of P450aromB transcript abundance have been reported in zebrafish (Danio rerio) juveniles exposed to EE 2 (Kazeto et al 2004, Vosges et al 2010 besides in the head of roach (Rutilus rutilus) at 28 and 56 days after spawning (Lange et al 2008). These findings indicate that metals and EE 2 could disrupt the HPLG axis by non specific mechanism.…”
Section: Discussionmentioning
confidence: 77%