4.6 Article

In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.cbpc.2017.06.002

关键词

Alkaline phosphatase; Bioassay; Endocrine disrupting compounds; Estradiol; Fish scales; Tartrate-resistant acid phosphatase

资金

  1. Foundation for Science and Technology of Portugal (FCT) [PTDC/AAG-GLO/4003/2012]
  2. [CCMAR/Multi/04326/2013]
  3. [SFRH/BPD/84033/2012]
  4. Fundação para a Ciência e a Tecnologia [PTDC/AAG-GLO/4003/2012] Funding Source: FCT

向作者/读者索取更多资源

A wide range of estrogenic endocrine disruptors (EDCs) are accumulating in the environment and may disrupt the physiology of aquatic organisms. The effects of EDCs on fish have mainly been assessed using reproductive endpoints and in vivo animal experiments. We used a simple non-invasive assay to evaluate the impact of estrogens and EDCs on sea bass (Dicentrarchus labrax) and tilapia (Oreochromis mossambicus) scales. These were exposed to estradiol (E2), two phytoestrogens and six anthropogenic estrogenic/anti-estrogenic EDCs and activities of enzymes related to mineralized tissue turnover (TRAP, tartrate-resistant acid phosphatase and ALP, alkaline phosphatase) were measured. Semi-quantitative RT-PCR detected the expression of both membrane and nuclear estrogen receptors in the scales of both species, confirming scales as a target for E2 and EDCs through different mechanisms. Changes in TRAP or ALP activities after 30 minute and 24 h exposure were detected in sea bass and tilapia scales treated with E2 and three EDCs, although compound-, time- and dose-specific responses were observed for the two species. These results support again that the mineralized tissue turnover of fish is regulated by estrogens and reveals that the scales are a mineralized estrogen-responsive tissue that may be affected by some EDCs. The significance of these effects for whole animal physiology needs to be further explored. The in vitro fish scale bioassay is a promising non-invasive screening tool for E2 and EDCs effects, although the low sensitivity of TRAP/ALP quantification limits their utility and indicates that alternative endpoints are required.

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