E. Escartin et C. Porte, BIOACCUMULATION, METABOLISM, AND BIOCHEMICAL EFFECTS OF THE ORGANOPHOSPHORUS PESTICIDE FENITROTHION IN PROCAMBARUS-CLARKII, Environmental toxicology and chemistry, 15(6), 1996, pp. 915-920
Fenitrothion (O, O-dimethyl O-(3-methyl-4-nitrophenyl) phosphorothioat
e) is readily taken up from the water by the crayfish Procambarus clar
kii. The bioconcentration factor, however, is lower than expected on t
he basis of its octanol/water partition coefficient. The ability of P.
clarkii to metabolize fenitrothion was evaluated in vitro by using 12
,000-g supernatant or microsomal fractions isolated from hepatopancrea
s and the results pointed out the existence of both oxidative and glut
athione-mediated metabolism. Several biomarkers of exposure viz., the
microsomal mixed-function oxygenase system, a phase II enzyme [glutath
ione S-transferase], and acetylcholinesterase inhibition, were studied
in organisms exposed to 20 mu g/L of fenitrothion for 48 h. Cytochrom
e P450 content, NADPH cytochrome c(P450) reductase, and 7-ethoxyresoru
fin O-deethylase activity showed significant induction the second day
of treatment, whereas glutathione S-transferase activity appeared to b
e unaffected. Acetylcholinesterase activity in the neuromuscular tissu
e of P. clarkii was a good indicator of exposure to this compound.