A FIELD-EVALUATION OF CYTOCHROME-P4501A AS A BIOMARKER OF CONTAMINANTEXPOSURE IN 3 SPECIES OF FLATFISH

Citation
Tk. Collier et al., A FIELD-EVALUATION OF CYTOCHROME-P4501A AS A BIOMARKER OF CONTAMINANTEXPOSURE IN 3 SPECIES OF FLATFISH, Environmental toxicology and chemistry, 14(1), 1995, pp. 143-152
Citations number
46
Categorie Soggetti
Toxicology,"Environmental Sciences",Chemistry
ISSN journal
07307268
Volume
14
Issue
1
Year of publication
1995
Pages
143 - 152
Database
ISI
SICI code
0730-7268(1995)14:1<143:AFOCAA>2.0.ZU;2-K
Abstract
A study was conducted over the course of a year to determine the induc tion of hepatic cytochrome P4501A (CYP1A) in three species of benthic fish collected from a contaminated site compared to fish sampled from a less-contaminated site. Juvenile fish were used to minimize effects of reproductive status and migration. CYP1A was determined by two cata lytic assays [aryl hydrocarbon hydroxylase (AHH) and ethoxyresorufin O -deethylase (EROD)I and by an immunoassay (ELISA) utilizing polyclonal antibodies raised against purified CYP1A from cod. AHH activities wer e measured by a standard method (AHH(std)) and by two variations of th e standard method. All three primary CYP1A measures (AHH(std), EROD, a nd ELISA) showed consistent between-site differences, indicating that induction of CYP1A can be a reliable biomarker of contaminant exposure in fish if appropriate biological variables are controlled for in fie ld studies. Multiple ANOVA demonstrated that the AHH(std) and ELISA da ta showed less variability due to species or temporal differences, and less unexplained variability, compared to the data from the EROD assa y or either variation of the AHH assay. For all measures, variability associated with site differences far outweighed species or temporal va riability. Immunoassay, while less sensitive than the AHH(std) assay, is nonetheless recommended to be used in conjunction with catalytic as says because of the potential for samples to lose catalytic activity i f not handled properly. The current results suggest that the lower non contaminant-related variability of AHH(std) makes this CYP1A measure p otentially more useful for monitoring programs in which analysis of tr ends is a primary goal.