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« Previous AbstractBioavailability of insect neuropeptides: the PK/PBAN family as a case study    Next Abstract"An oleate-stimulated, phosphatidylinositol 4,5-bisphosphate-independent phospholipase D in Schizosaccharomyces pombe" »

FEBS J


Title:Bioavailability of backbone cyclic PK/PBAN neuropeptide antagonists--inhibition of sex pheromone biosynthesis elicited by the natural mechanism in Heliothis peltigera females
Author(s):Hariton A; Ben-Aziz O; Davidovitch M; Altstein M;
Address:"Department of Entomology, The Volcani Center, Bet Dagan, Israel"
Journal Title:FEBS J
Year:2010
Volume:20100120
Issue:4
Page Number:1035 - 1044
DOI: 10.1111/j.1742-4658.2009.07547.x
ISSN/ISBN:1742-4658 (Electronic) 1742-464X (Linking)
Abstract:"The bioavailability (i.e. ability to penetrate the insect cuticle, to reach the target organ and to exert bioactivity) of two backbone cyclic (BBC) pyrokinin/pheromone biosynthesis-activating neuropeptide (PK/PBAN) antagonistic peptides was tested by applying them topically to Heliothis peltigera females and monitoring the resulting inhibition of sex pheromone production elicited by the natural (endogenous) mechanism during scotophase. Peptides were applied at various time points before the onset of scotophase, in aqueous or organic solvents, and pheromone content was examined at the 5th or 6th hour of scotophase. Both peptides penetrated the cuticle very efficiently and inhibited sex pheromone biosynthesis elicited by the natural mechanism for up to 8 or 9 h after application. The degree of inhibition differed between solvents: those applied in double-distilled water (DDW) were more active than those applied in dimethylsulfoxide (inhibition by 53-73% and 15-38%, respectively, for BBC-25, and 46-67% and 36-40%, respectively for BBC-28). Peptides applied in dimethylsulfoxide and hexane exhibited slightly more persistent inhibitory activity than those applied in DDW. The solvents themselves did not affect sex pheromone production. Multiple applications (at -2, 0, +2 and +4 h) resulted in almost complete (87%) inhibition of sex pheromone biosynthesis, compared with 52% inhibition following a single application. The present study is the first demonstration of the ability of topically applied PK/PBAN antagonists to inhibit sex pheromone biosynthesis elicited by the natural mechanism in female moths, and provides important information on the bioavailability of BBC peptides and the mechanism responsible for sex pheromone production in these insects"
Keywords:"Administration, Topical Animals Biological Availability Female Moths/drug effects/*metabolism Neuropeptides/*pharmacokinetics/pharmacology Peptides, Cyclic/*pharmacokinetics/pharmacology Sex Attractants/*antagonists & inhibitors/biosynthesis/metabolism So;"
Notes:"MedlineHariton, Aliza Ben-Aziz, Orna Davidovitch, Michael Altstein, Miriam eng Research Support, Non-U.S. Gov't England 2010/01/22 FEBS J. 2010 Feb; 277(4):1035-44. doi: 10.1111/j.1742-4658.2009.07547.x. Epub 2010 Jan 20"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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