© 1986 Oxford University Press
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Sublethal Acute Toxicity of Carbosulfan [2,3-dihydro-2,2-dimethyl-7-benzofuranyl(di-n-butylaminosulfenyl)(methyl)carbamate] in the Rat after Intravenous and Oral Exposures
Department of Veterinary Science and WOI Regional Program in Veterinary Medical Education, University of Idaho Moscow, Idaho 83843
Sublethal Acute Toxicity of Carbosulfan [2,3-dihydro-2,2-dimethyl-7-benzofuranyl(di-n-butylaminosulfenyl)(methyl)carbamate] in the Rat after Intravenous and Oral Exposures. RENZI, B. E., AND KRIEGER, R. I. (l986). Fundwn. Appl. Toxicol. 6, 7–15. Sublethal toxicity of carcarbosulfan, 2,3-dihydro-2,2-dimethyl-benzofuranyl(di-n-butylaminosulfenyl)(methyl)carbamate, was evaluated in female Sprague-Dawley rats. Erythrocyte acetylcholinesterase (AChE) activity was maximally inhibited 1 min after iv administration (38, 23, and 15% of pretreatment activity after 86, 250, and 690 µg/kg, respectively) and recovered by 4 hr. Maximum AChE inhibition (63% of pretreatment activity) was measured 45 min after oral dosing (690 µg/kg) and activity recovered after 5 hr. Signs included urination, defecation, facial muscle fasciculations, salivation, and tremors. Carbosulfan was less toxic when given orally. Metabolic activation of carbosulfan to carbofuran (2,3-dihydro-2,2-dimethyl-7-benzofuranol methylcarbamate) was in vestigated by measuring plasma concentrations 4, 30, and 240 min after iv (80–120 or 620–640 µg/kg) and oral (540–700 or 2030–2190 µ/kg) dosages of [carbonyl-14C]carbosulfan. Peak plasma concentrations were measured at 4 and 30 min after iv and oral exposure, respectively. Carbosulfan was rapidly activated to carbofuran. Reduction in AChE activity was better correlated (r = 0.97) with plasma concentration of [carbosulfan + carbofuran] and plasma carbofuran (r = 0.96) than with plasma carbosulfan (r = 0.73). Signs generally occurred when AChE activity was less than 65% of pretreatment levels, corresponding to 40 pmol/ml [carbosulfan + carbofuran] in plasma. Based on regression analysis and metabolic studies, both carbosulfan and carbofuran contributed to the observed AChE inhibition; however, carbofuran, a more potent in vitro inhibitor and the usual predominant inhibitor in plasma, was responsible for most of the erythrocyte AChE inhibition.