Ml. Haasch et al., CAGED AND WILD FISH - INDUCTION OF HEPATIC CYTOCHROME-P-450 (CYP1A1) AS AN ENVIRONMENTAL BIOMONITOR, Environmental toxicology and chemistry, 12(5), 1993, pp. 885-895
Hepatic monooxygenase activity can be induced by many different enviro
nmental chemical contaminants, and measurement of this activity has be
en proposed as an environmental biomonitor. Using in situ caged catfis
h and largemouth bass, and collected wild killifish, environmental ind
uction of hepatic CYP1A1 was investigated using catalytic enzyme assay
s, regiospecific metabolism, immunodetection, and nucleic acid hybridi
zation. The purpose of these studies was to evaluate these techniques
for detection of CYP1A1 induction as a potential environmental biomoni
tor of environmental chemical contamination. Exposure of catfish in ca
ges to polyaromatic hydrocarbon-(PAH-) and polychlorinated biphenyl- (
PCB-) contaminated river water for two, four, or six weeks resulted in
fourfold increases in ethoxyresorufin-0-deethylase (EROD) activity an
d three- and fivefold increases in immunoreactive CYP1A1 protein and h
ybridizable CYP1A1 mRNA, respectively, when compared to laboratory wat
er control values. Hybridizable CYP1A1 mRNA in caged largemouth bass i
ncreased 5. 1-fold at 1 d of exposure. Caged largemouth bass had 5-, 1
.4-, and 0.8-fold increases at 3 d and 6-, 2.4-, 0.4-fold increases at
7 d of river water exposure in EROD, immunoreactive CYP1A1 protein, a
nd CYP1A1 mRNA, respectively, when compared to laboratory water contro
l values. Livers of killifish from a 2,3,7,8-tetrachlorodibenzo-p-diox
in-contaminated area had threefold higher EROD activity and similarly
elevated immunoreactive CYP1A1 protein, a two- to fourfold increase in
CYP1A1 mRNA, and a four- to eightfold increase in 6beta-hydroxyproges
terone activity, when compared to killifish livers sampled from a ''cl
ean'' site. These results indicate that catalytic activity measurement
s, immunodetection, and nucleic acid hybridization may be used to dete
ct environmental hepatic CYP1A1 induction in fish, and may be useful f
or the biomonitoring or screening of selected environments for chemica
l contamination.