The long-term goal of the proposed study is to elucidate the mechanism by which neuroactive insecticides exert their toxic actions.
The specific aims of the proposed renewal application are to elucidate the physiological mechanisms that underlie the selective toxicity of several selected newer insecticides between mammals and insects. Most insecticides are much more toxic to insects than to mammals, and the mechanism of selective toxicity lies in many cases in differential actions on the target neuroreceptors/ion channels. Although recent developments and applications of molecular biology and genetics techniques have identified the molecular structures such as amino acid compositions of target receptors/channels that are deemed responsible for differential actions, almost nothing is known about how the differential actions are brought about as a result of the difference in molecular structures. Our working hypothesis is that the differential actions of insecticides on the target receptor/channels of mammals and insects could be caused by some difference in the kinetics of receptors/channels. For example, insecticide modification of the channel may be dependent upon the channel open or closed state, the kinetics of insecticide binding and unbinding, the temperature coefficient, etc. In order to elucidate the physiological mechanisms of selective toxicity, patch clamp data on the kinetics of receptors/channels and those of insecticide modification will be compared between rat and cockroach neurons for fipronil modulation of GABA receptors, imidacloprid modulation of neuronal nicotinic acetylcholine receptors (nnAChRs), spinosad modulation of nnAChRs and GABA receptors, and indoxacarb modulation of sodium channels, nnAChRs and GABA receptors. The results thus obtained are expected to answer the question of how selective toxicity between mammals and insects can be explained in terms of the differential actions on the target receptors/channels. This information will significantly contribute to the development of newer therapeutic means of insecticide intoxication of humans and of more effective and safer insecticides.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS014143-27
Application #
6777454
Study Section
Alcohol and Toxicology Subcommittee 4 (ALTX)
Program Officer
Jett, David A
Project Start
1978-05-01
Project End
2006-06-30
Budget Start
2004-08-01
Budget End
2006-06-30
Support Year
27
Fiscal Year
2004
Total Cost
$367,500
Indirect Cost
Name
Northwestern University at Chicago
Department
Pharmacology
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Narahashi, Toshio; Zhao, Xilong; Ikeda, Tomoko et al. (2010) Glutamate-activated chloride channels: Unique fipronil targets present in insects but not in mammals. Pestic Biochem Physiol 97:149-152
Peterson, Randall T; Nass, Richard; Boyd, Windy A et al. (2008) Use of non-mammalian alternative models for neurotoxicological study. Neurotoxicology 29:546-55
Narahashi, T; Zhao, X; Ikeda, T et al. (2007) Differential actions of insecticides on target sites: basis for selective toxicity. Hum Exp Toxicol 26:361-6
Zhao, Xilong; Yeh, Jay Z; Salgado, Vincent L et al. (2005) Sulfone metabolite of fipronil blocks gamma-aminobutyric acid- and glutamate-activated chloride channels in mammalian and insect neurons. J Pharmacol Exp Ther 314:363-73
Zhao, Xilong; Ikeda, Tomoko; Salgado, Vincent L et al. (2005) Block of two subtypes of sodium channels in cockroach neurons by indoxacarb insecticides. Neurotoxicology 26:455-65
Ikeda, Tomoko; Nagata, Keiichi; Kono, Yoshiaki et al. (2004) Fipronil modulation of GABAA receptor single-channel currents. Pest Manag Sci 60:487-92
Zhao, Xilong; Salgado, Vincent L; Yeh, Jay Z et al. (2004) Kinetic and pharmacological characterization of desensitizing and non-desensitizing glutamate-gated chloride channels in cockroach neurons. Neurotoxicology 25:967-80
Zhao, Xilong; Yeh, Jay Z; Salgado, Vincent L et al. (2004) Fipronil is a potent open channel blocker of glutamate-activated chloride channels in cockroach neurons. J Pharmacol Exp Ther 310:192-201
Zhao, Xilong; Ikeda, Tomoko; Yeh, Jay Z et al. (2003) Voltage-dependent block of sodium channels in mammalian neurons by the oxadiazine insecticide indoxacarb and its metabolite DCJW. Neurotoxicology 24:83-96
Ikeda, Tomoko; Zhao, Xilong; Kono, Yoshiaki et al. (2003) Fipronil modulation of glutamate-induced chloride currents in cockroach thoracic ganglion neurons. Neurotoxicology 24:807-15

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