INTERACTIVE EFFECTS BETWEEN EBI FUNGICIDES (PROCHLORAZ, PROPICONAZOLEAND PENCONAZOLE) AND OP INSECTICIDES (DIMETHOATE, CHLORPYRIFOS, DIAZINON AND MALATHION) IN THE HYBRID RED-LEGGED PARTRIDGE
G. Johnston et al., INTERACTIVE EFFECTS BETWEEN EBI FUNGICIDES (PROCHLORAZ, PROPICONAZOLEAND PENCONAZOLE) AND OP INSECTICIDES (DIMETHOATE, CHLORPYRIFOS, DIAZINON AND MALATHION) IN THE HYBRID RED-LEGGED PARTRIDGE, Environmental toxicology and chemistry, 13(4), 1994, pp. 615-620
The toxicokinetic interactions between the ergosterol-biosynthesis-inh
ibiting (EBI) fungicides prochloraz, propiconazole, and penconazole an
d the organophosphorus (OP) insecticides dimethoate, chlorpyrifos, and
diazinon have been studied in the hybrid red-legged partridge. The in
hibition of serum butyrylcholinesterase (BuChE) activity provided a us
eful biochemical indicator of the generation of the toxic oxon metabol
ites of these OP insecticides. Birds pretreated with 180 mg/kg prochlo
raz tended to show a greater inhibition of serum BuChE activity at 1,
4, and 24 h following oral exposure to either of the OPs dimethoate (3
mg/kg) or chlorpyrifos (9 mg/kg) compared to birds pretreated with co
rn oil. Prochloraz-pretreated birds also showed a tendency toward an i
ncreased inhibition at 24 h following dosing with the OP diazinon (4.3
mg/kg) compared to corn oil controls. In the case of dimethoate, the
inhibition of serum BuChE activity was significantly greater in treate
d birds than controls at 24 h. Birds pretreated with the EBI fungicide
propiconazole (200 mg/kg) showed a similar inhibition of serum BuChE
activity to those pretreated with corn oil following administration of
167 mg/kg malathion. Pretreatment with the EBI fungicide penconazole
(200 mg/kg) produced significantly greater depression of serum BuChE a
ctivity at 1, 4, and 24 h after dosing with malathion, when compared t
o corn oil controls. The tendency toward increased inhibition of serum
BuChE activity by each of the OPs in prochloraz-pretreated birds was
attributed to an increased activation of the compound to its active ox
on form as a consequence of induction of microsomal monooxygenases by
prochloraz.