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Testosterone and energy metabolism in the estuarine mysid Neomysis integer (Crustacea: Mysidacea) following exposure to endocrine disruptors
Verslycke, T.; Poelmans, S.; De Wasch, K.; De Brabander, H.; Janssen, C.R. (2004). Testosterone and energy metabolism in the estuarine mysid Neomysis integer (Crustacea: Mysidacea) following exposure to endocrine disruptors. Environ. Toxicol. Chem. 23(5): 1289-1296. hdl.handle.net/10.1897/03-338
In: Environmental Toxicology and Chemistry. Setac Press: Elmsford NY. ISSN 0730-7268, more
Peer reviewed article

Available in Authors 
    VLIZ: Open Repository 247725 [ OMA ]

Keywords
    Biomarkers; Energy metabolism; Growth; Induction; Toxicity; Neomysis integer (Leach, 1814) [WoRMS]; Brackish water
Author keywords
    Testosterone metabolism; Endocrine disruption

Authors  Top 
  • De Brabander, H., more
  • Janssen, C.R., more

Abstract
    A diverse set of reference compounds suspected of having an endocrine-disrupting mode of action (i.e., testosterone, flutamide, ethinylestradiol, precocene, nonylphenol, fenoxycarb, and methoprene) were tested for acute toxicity to the estuarine mysid Neomysis integer (Crustacea: Mysidacea). Neomysis integer was very sensitive to all tested compounds, with 96-h median lethal concentrations in a narrow range between 0.32 and 1.95 mg/L. The pesticides methoprene and fenoxycarb, both synthetic insect juvenile hormone analogs, were most toxic to N. integer. In addition, the short-term sublethal effects of methoprene and nonylphenol (an estrogen agonist) on the energy and steroid metabolism of N. integer were evaluated. Both compounds significantly affected energy and testosterone metabolism of N. integer at concentrations below acute toxicity levels. Energy consumption in methoprene- and nonylphenol-exposed mysids was significantly induced at 100 µg/L, resulting in a lower cellular energy allocation in these animals. Testosterone phase I metabolism was affected at 10 µg/L, whereas glycosylation was the most important phase II pathway affected in mysids exposed to 100 µg/L of both compounds. Methoprene exposure resulted in a concentration-dependent increase in the metabolic androgenization ratio. Mysids exposed to nonylphenol at 10 µg/L had a significantly higher metabolic androgenization ratio. The present study indicates that energy and testosterone metabolism of mysids, as endpoints, are able to detect endocrine-disruptive activity of chemicals after short-term exposure to environmentally realistic levels of endocrine disruptors.

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