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Title: Comparative metabolism and fate of fenvalerate in Japanese quail (Coturnix coturnix japonica) and rats (Rattus norwegicus)

Journal Article · · J. Agric. Food Chem.; (United States)
DOI:https://doi.org/10.1021/jf00072a001· OSTI ID:6698613

Adult Japanese quail were administered 100 mg/kg chlorophenyl-labeled (/sup 14/C)fenvalerate, ..cap alpha..-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate, for study of its distribution, elimination, and metabolism. Ninety percent of the administered dose was eliminated in the excreta within the first 24 h. In addition to fenvalerate, the following metabolites were present: benzeneacetic acid, 4-chloro-..cap alpha..-(1-methylethyl)-,cyano(3-phenoxy-4-hydroxyphenyl)methyl ester (4'-OH-fenvalerate); benzeneacetic acid, 4-chloro-..cap alpha..-(1-methylethyl)-,(aminocarbonyl)(3-phenoxyphenyl)methyl ester (CONH/sub 2/-fenvalerate); 4-chloro-..cap alpha..-(1-methylethyl)benzeneacetic acid(Cl-V acid); 4-chloro-..cap alpha..-(2-hydroxy-1-methylethyl)benzeneacetic acid(4-OH-Cl-V acid). In time course studies radiocarbon peaked at 3 h (9..mu..g/g) in the liver and gradually declined, while in the blood it peaked within 2 h and fell quickly to an equilibrium value of 1.5 ..mu..g/mL blood. In liver microsomal and isolated heptatocyte preparations of Japanese quail and rat, the following metabolites were identified: Cl-V acid, 4-OH-Cl-V acid, 4'-OH-fenvalerate, CONH/sub 2/-fenvalerate. Oxidation was found to be the predominant route of degradation either pre- or post-hydrolysis of the parent compound. Rapid excretion, lesser absorption, and faster metabolism probably explain the lower toxicity of fenvalerate to birds compared to rats.

Research Organization:
Univ. of Maryland, College Park
OSTI ID:
6698613
Journal Information:
J. Agric. Food Chem.; (United States), Vol. 34:6
Country of Publication:
United States
Language:
English