The long-term objective of this proposal 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 determining the relative roles of hepatic and extrahepatic biotransformation of these chemicals in mediating their acute toxcicities. Implicit in this approach is the evaluation of numerous factors which affect these critical metabolic pathways. It is expected that these studies will provide information useful in assessing the health hazards of organothiophosphate insecticides, as well as their potential for toxic interactions with certain other zenobiotics. Furthermore these studies will contribute to the fundamental knowledge of those metabolic systems involved in the biotransformation of organothiophosophate insecticides.
The specific aims to be addressed in this research are as follows: 1. To further investigate whether the toxic oxygen analogs produced intrahepatically from organothiophosphate pesticides enter the general circulation, or whether they undergo extensive intrahepatic detoxification thereby preventing their escape from the liver. 2. To determine if the A-esterase in blood has the capacity to prevent the passage of those oxons escaping liver to target tissues such as brains and lungs. 3. To investigate the toxicological significance to extrahepatic activation of certain organothiophosphate insecticides. 4. To identify and characterize the metabolic activation and detoxification of organothiophosphate insecticides by human placenta. 5. To evaluate the role of gluthathione-mediated biotransformation of dimethyl-substituted organothiophosphates in vivo in the detoxification of these pesticides.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES004335-04
Application #
3252429
Study Section
Toxicology Study Section (TOX)
Project Start
1986-08-01
Project End
1991-08-31
Budget Start
1989-09-01
Budget End
1990-08-31
Support Year
4
Fiscal Year
1989
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
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
Sultatos, L G (1994) Mammalian toxicology of organophosphorus pesticides. J Toxicol Environ Health 43:271-89
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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