The long-term objective of this project is to supply information which will aid in the identification of conditions under which individuals might be susceptible to organothiophosphate pesticide-induced toxicity. It seeks to accomplish this objective by focusing on how hepatic and extrahepatic metabolic activation and detoxification of these pesticides mediate their toxicity. The relative activation and detoxification of organothiophosphate pesticides at sites of entry and, after absorption, at various internal organs could greatly influence the severity and time course of their toxicity. Understanding the interactions of other foreign compounds with organothiophosphates following different routes of exposure requires knowledge of the relationships of metabolism of these pesticides by different tissues. This research will not only provide information helpful in the safety assessment of pesticides, but will also contribute to the fundamental knowledge of those metabolic systems involved in the biotransformation of these pesticides.
Specific aims to be addressed in this research are: 1. To evaluate if the toxic oxygen analogs produced hepatically from organothiophosphates escape the liver, thereby entering the general circulation, or are these potent cholinesterase inhibitors further biotransformed hepatically, inactivating them before they exit the liver; 2. If the toxic oxygen analogs of organothiophosphates escape the liver and enter the blood, can they survive long enough to reach extrahepatic organs, or will they quickly be detoxified by plasma A-esterases; 3. To evaluate the toxicological significance of extrahepatic activation of organothiophosphate pesticides with particular emphasis on the brain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES004335-02
Application #
3252428
Study Section
Toxicology Study Section (TOX)
Project Start
1986-08-01
Project End
1988-12-31
Budget Start
1987-08-01
Budget End
1988-12-31
Support Year
2
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Type
Schools of Medicine
DUNS #
605799469
City
Newark
State
NJ
Country
United States
Zip Code
07107
Agyeman, A A; Sultatos, L G (1998) The actions of the H2-blocker cimetidine on the toxicity and biotransformation of the phosphorothioate insecticide parathion. Toxicology 128:207-18
Ramos, S; Sultatos, L (1998) Flavonoid-induced alterations in cytochrome P450-dependent biotransformation of the organophosphorus insecticide parathion in the mouse. Toxicology 131:155-67
Berger Jr, C W; Sultatos, L G (1997) The effects of the phosphorothioate insecticide fenitrothion on mammalian cytochrome P450-dependent metabolism of estradiol. Fundam Appl Toxicol 37:150-7
Vitarius, J A; O'Shaughnessy, J A; Sultatos, L G (1995) The effects of phenobarbital pretreatment on the metabolism and toxicity of paraoxon in the mouse. Pharmacol Toxicol 77:16-22
Vitarius, J A; Sultatos, L G (1995) The role of calcium in the hydrolysis of the organophosphate paraoxon by human serum A-esterase. Life Sci 56:125-34
O'Shaughnessy, J A; Sultatos, L G (1995) Interaction of ethanol and the organophosphorus insecticide parathion. Biochem Pharmacol 50:1925-32
Sultatos, L G (1994) Mammalian toxicology of organophosphorus pesticides. J Toxicol Environ Health 43:271-89
Vitarius, J A; Sultatos, L G (1994) Kinetic mechanism of the detoxification of the organophosphate paraoxon by human serum A-esterase. Drug Metab Dispos 22:472-8
Huang, Y S; Woods, L; Sultatos, L G (1994) Solubilization and purification of A-esterase from mouse hepatic microsomes. Biochem Pharmacol 48:1273-80
Huang, Y S; Sultatos, L G (1993) Glutathione-dependent biotransformation of methyl parathion by mouse liver in vitro. Toxicol Lett 68:275-84

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