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  • Title: Potentiations of N-methylcarbamate toxicities by organophosphorus insecticides in male mice.
    Author: Takahashi H, Kato A, Yamashita E, Naito Y, Tsuda S, Shirasu Y.
    Journal: Fundam Appl Toxicol; 1987 Feb; 8(2):139-46. PubMed ID: 2951289.
    Abstract:
    A N-methylcarbamate insecticide, 2-sec-butylphenyl N-methylcarbamate (BPMC), is markedly potentiated by low-dose treatments of P = S type organophosphorus insecticides. As a mechanism of this potentiation, the increase of plasma BPMC concentrations due to the inhibited metabolic degradation has been suggested. In this study, acute toxicities of five N-methylcarbamates structurally related to BPMC were studied after low-dose treatments of three P = S type organophosphorus insecticides (cyanophos, fenitrothion, and malathion) and one P = O type organophosphorus insecticide (dichlorvos), and the role of plasma concentrations of N-methylcarbamates in the potentiations was examined. Acute toxicities of five N-methylcarbamates were potentiated by the treatments of the P = S types, among which the potentiation of BPMC was strongest. BPMC toxicity was not potentiated by the treatment of the P = O type. Plasma concentrations of BPMC were increased by the treatments of the P = S types, but not by the treatment of the P = O type. The acute toxicity and plasma concentrations of BPMC were increased by SKF 525-A (an inhibitor of mixed-function oxidase). These results suggest that the increase of plasma BPMC concentrations may be related to the potentiation of BPMC toxicity. The treatment of fenitrothion increased plasma concentrations of other N-methylcarbamates more than those of BPMC, although the potentiation of BPMC toxicity was strongest. SKF 525-A and fenitrothion treatments increased plasma BPMC concentrations to a similar degree, but the potentiation of BPMC toxicity by SKF 525-A was significantly less than that by fenitrothion. Thus, some other mechanism(s) may be responsible for the potentiations of the N-methylcarbamate toxicities.
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