A non-destructive in ovo assay to quantify EROD activity in embryo-larval Fundulus heteroclitus
- Environmental Protection Agency, Narragansett, RI (United States)
- Rutgers Univ., Piscataway, NJ (United States)
Sensitive embryo-larval estuarine fish exposed to organic contaminants such as polyaromatic hydrocarbons and polyhalogenated aromatic hydrocarbons (PHAHs) have been shown to demonstrate characteristic biochemical responses, and impaired development and reduced survival. One of the best studied of these biochemical responses is induction of cytochrome P450 enzymes, e.g., CYP1A, frequently assessed as ethoxyresorufin-o-deethylase (EROD) activity. Standard methods to measure EROD activity in embryo-larval fish require destructive samples, composited from many embryos, precluding information on individual variation in EROD activity or concurrent observation of health effects. A novel method has been developed that employs the non-destructive observation in individual embryos of EROD activity, demonstrated by the production and accumulation in the embryonic bladder of the fluorescent product, resorufin. EROD activity in a living embryo is quantified by bladder fluorescence using microfluorometric instrumentation. Using this technique, the authors were able to follow individual fish throughout embryonic and early larval development making temporal observations of EROD activity as well as developmental progress, lesion characterization, hatch rate and success, and post-hatch growth and survival. Results were used to examine differential responsiveness to EROD-inducing organic contaminants of embryo-larval fish from parental populations inhabiting PHAH-contaminated or uncontaminated environments.
- OSTI ID:
- 458292
- Report Number(s):
- CONF-961149--
- Country of Publication:
- United States
- Language:
- English
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