Effect of certain halogenated hydrocarbon insecticides on cyclic adenosine 3',5'-monophosphate-3H formation by rat kidney cortex.
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The introduction of the anticoagulants in the early 1950s, with their much greater safety to nontarget animals, resulted in a general decline in the use of single-dose rodenticides. However, the appearance of rodent resistance to the anticoagulants, first in the United Kingdom, later elsewhere in Europe, and still more recently in the USA, has revived interest in the use of single-dose rodenticides. Unfortunately, owing to their danger to nontarget mammals, the use of several of these compounds must be restricted; others, despite their long use, are now recognized to be unsatisfactory because of their poor acceptance or reacceptance by rats and mice. Thus, only very few compounds of this type are available for unrestricted use and there is an urgent need for the development of effective alternatives.
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Extensive residue studies have been done with most of the organochlorine insecticides. The brain is a reliable tissue to determine lethal or exposure residues of the persistent organochlorine insecticides. Fewer studies have been done with organophosphate residues. residues of organophosphate insecticides are useful indicators of poisoning in tissues of exposed animals. Metabolite determination and identification is a necessary consideration since metabolic activation is required for several of the organophosphate insecticides. No studies of tissue residue evaluation of carbamate insecticides are available.
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