The Metabolism of Co-Ral (Bayer 21/199) by Tissues of the House Fly, Cattle Grub, Ox, Rat, and Mouse1
- 31 July 1959
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Economic Entomology
- Vol. 52 (4) , 692-695
- https://doi.org/10.1093/jee/52.4.692
Abstract
In mammals, the liver is primarily responsible for Co-ral metabolism. In the mouse, which is susceptible to Co-ral® (O,O- diethyl O-(3-chloro-4-methylumbelliferone) phosphorothionate) the compound is activated, and there are no degrading systems. In the ox and rat, which are resistant to Co-ral, the compound is degraded. It has been shown for the ox that both an activating and a degrading system are in the liver, but the latter is more potent. In the house fly (Musca domestica L.), and cattle grub (Hypoderma bovis (L.)), which are susceptible to Co-ral, there is : activating but no degrading system. Activation by the cattle grub is associated with fat body and gut. The results account for the selective toxicity of Co-ral, and possibly for the fact that only dermal treatment controls cattle grubs in the ox.This publication has 7 references indexed in Scilit:
- New Organophosphate Insecticides Developed on Rational Principles1Journal of Economic Entomology, 1958
- Fate of P32-Labeled Bayer 21/199 in the White Rat1Journal of Economic Entomology, 1958
- Properties and Metabolism in the Cockroach and Mouse of Malathion and Malaoxon1Journal of Economic Entomology, 1957
- The conversion of schradan (OMPA) and parathion into inhibitors of cholinesterase by mammalian liverBiochemical Journal, 1955
- Tests with Some Phosphorus Compounds against Cattle Grubs1Journal of Economic Entomology, 1955
- New Insecticides for Control of the Cattle GrubJournal of Economic Entomology, 1954
- Some properties of specific cholinesterase with particular reference to the mechanism of inhibition by diethyl p-nitrophenyl thiophosphate (E 605) and analoguesBiochemical Journal, 1950