Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDynamic changes in ejaculatory bulb size during Drosophila melanogaster aging and mating    Next AbstractLNAPL source zone delineation using soil gases in a heterogeneous silty-sand aquifer »

Life Sci


Title:Chlorocyclohexane insecticides and male medfly attractants: similar stereospecificity for neuroactivity and interactions with a housefly [35S]t-butylbicyclophosphorothionate binding site
Author(s):Cohen E; Casida JE;
Address:
Journal Title:Life Sci
Year:1985
Volume:36
Issue:19
Page Number:1837 - 1842
DOI: 10.1016/0024-3205(85)90156-0
ISSN/ISBN:0024-3205 (Print) 0024-3205 (Linking)
Abstract:"[35S]t-Butylbicyclophosphorothionate [( 35S]TBPS) undergoes saturable specific binding to a membrane preparation from housefly thoraxes and abdomens with apparent Kd and Bmax values at equilibrium of 0.17 microM and 2.2 pmol/mg protein at 20 degrees C. Lindane is more potent than three other isomers of hexachlorocyclohexane as a toxicant for houseflies and in displacing [35S]TBPS from this housefly membrane preparation. This correlation of similar stereospecificity for neuroactivity and interaction with the TBPS receptor extends to the Mediterranean fruit fly male attractant trimedlure and its components and analogs. The relative attractancy of t-butyl cis-4-chloro-trans-2-methylcyclohexanecarboxylate and of three less active isomers of this trans-chlorocyclohexane-carboxylate parallel their potency in the [35S]TBPS binding assay. With both trimedlure and the related cyclohexene attractant siglure the trans-isomers are more potent than the cis-isomers as attractants and in displacing [35S]TBPS. Scatchard analyses indicate that lindane binds at the same site as [35S]TBPS. The hexachlorocyclohexane isomers and trimedlure components are much more potent inhibitors with membrane preparations from houseflies than from rat brain. The housefly TBPS receptor possibly serves as a model for the primary target sites, thereby suggesting that both the insecticide and the attractant may interact with some component of the putative GABAergic nervous or neuromuscular system"
Keywords:"Animals Brain/metabolism Bridged Bicyclo Compounds/*metabolism *Bridged Bicyclo Compounds, Heterocyclic Bridged-Ring Compounds/*metabolism Cyclohexanecarboxylic Acids/*metabolism Cyclohexenes *Diptera Female Hexachlorocyclohexane/*metabolism/toxicity Hous;"
Notes:"MedlineCohen, E Casida, J E eng P01 ES00049/ES/NIEHS NIH HHS/ Research Support, U.S. Gov't, P.H.S. Netherlands 1985/05/13 Life Sci. 1985 May 13; 36(19):1837-42. doi: 10.1016/0024-3205(85)90156-0"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 19-12-2024