""""""""Mode of Action and Metabolism of Organic Toxicants"""""""" is a concerted continuation program on pesticide chemistry and toxicology with three long-term objectives. The first is to define the chemistry and molecular toxicology of selected pesticides of concern because of actual or potential extensive human exposure with emphasis on elucidating their modes of action, biochemical target sites, and mechanisms of selective toxicity. The second objective is to design and develop chemical probes useful for furthering fundamental knowledge in the medical and agricultural sciences. The third is to improve the margins of safety for humans, other nontarget species and the environment in the essential uses of pest control chemicals.
The specific aims are embodied in five subprojects. The goals of the subproject on botanical insecticides and their analogs are to better understand the chemical toxicology of the established pyrethroids, rotenoids, ryanoids, veratridine alkaloids and isobutylamides and to devise ways of improving their potency and safety. Two subprojects focus on the toxicology and chemistry of GABA-gated chloride channel blockers. The toxicology emphasis is on the binding site of these channel blockers in mammals and insects and the physiological and metabolic aspects of their selective toxicity. The chemical studies consider the synthesis, structure-activity and degradation of many classes of insecticides acting at this site including the highly potent trioxabicyclooctanes and dithianes discovered in this Program Project. New radioligands and photoaffinity probes are also involved. The fourth subproject on organophosphorus pesticide toxicology is primarily concerned with the chemical and biological activation of the very extensively used thiophosphorus insecticides, the activated intermediates and biochemical targets of organophosphorus herbicides and fungicides, and the mechanisms and implications of sequential phosphorylation and alkylation reactions within the catalytic site of esterases important in delayed neurotoxicity and other long-term toxicological lesions. The last subproject considers the mammalian toxicology of herbicides and more specifically the acetyl CoA carboxylase target leading to a block in lipid synthesis, the glutathione-dependent processes in activation and detoxification, and the identification of the binding site of the herbicide endothall and the blister beetle toxicant cantharidin. This multidisciplinary program applies chemical, biochemical and toxicological methodologies to improving human and environmental health in the use of agricultural chemicals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Program Projects (P01)
Project #
5P01ES000049-30
Application #
2152867
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
1977-12-01
Project End
1997-11-30
Budget Start
1993-12-01
Budget End
1994-11-30
Support Year
30
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Zoology
Type
Schools of Earth Sciences/Natur
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Casida, John E; Quistad, Gary B (2004) Organophosphate toxicology: safety aspects of nonacetylcholinesterase secondary targets. Chem Res Toxicol 17:983-98
Sparks, S E; Quistad, G B; Li, W et al. (2000) Chloropicrin dechlorination in relation to toxic action. J Biochem Mol Toxicol 14:26-32
Tomizawa, M; Casida, J E (1999) Minor structural changes in nicotinoid insecticides confer differential subtype selectivity for mammalian nicotinic acetylcholine receptors. Br J Pharmacol 127:115-22
Fang, N; Casida, J E (1999) New bioactive flavonoids and stilbenes in cube resin insecticide. J Nat Prod 62:205-10
Sparks, S E; Quistad, G B; Casida, J E (1999) Organophosphorus pesticide-induced butyrylcholinesterase inhibition and potentiation of succinylcholine toxicity in mice. J Biochem Mol Toxicol 13:113-8
Fang, N; Casida, J E (1999) Cube resin insecticide: identification and biological activity of 29 rotenoid constituents. J Agric Food Chem 47:2130-6
Latli, B; D'Amour, K; Casida, J E (1999) Novel and potent 6-chloro-3-pyridinyl ligands for the alpha4beta2 neuronal nicotinic acetylcholine receptor. J Med Chem 42:2227-34
Schneider, M; Quistad, G B; Casida, J E (1999) Glutathione activation of chloropicrin in the Salmonella mutagenicity test. Mutat Res 439:233-8
Staub, R E; Quistad, G B; Casida, J E (1999) S-methyl N-butylthiocarbamate sulfoxide: selective carbamoylating agent for mouse mitochondrial aldehyde dehydrogenase. Biochem Pharmacol 58:1467-73
Schuler, F; Yano, T; Di Bernardo, S et al. (1999) NADH-quinone oxidoreductase: PSST subunit couples electron transfer from iron-sulfur cluster N2 to quinone. Proc Natl Acad Sci U S A 96:4149-53

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