Literature DB >> 24248519

Electrophysiological and behavioral responses of turnip moth males,Agrotis segetum to fluorinated pheromone analogs.

W Wenqi1, M Bengtsson, B S Hansson, T Liljefors, C Löfstedt, G D Prestwich, W C Sun, M Svensson.   

Abstract

The electrophysiological and behavioral responses of maleAgrotis segetum to fluorinated analogs of (Z)-5-decenyl acetate (Z5-10∶OAc) were investigated. The single sensillum recordings showed that 4,4-difluoro-(Z)-5-decenyl acetate (4,4-F2), 7,7-difluoro-(Z)-5-decenyl acetate (7,7-F2), 10,10,10-trifluoro-(Z)-5-decenyl acetate (10,10,10-F3) and 7,7,8,8-tetrafluoro-(Z)-5-decenyl acetate (7,7,8,8-F4) were each 100-fold less active than the natural Z5-10 ∶ OAc, whereas the 7,7,8,8,9,9,10,10,10-nonafluoro-(Z)-5-decenyl acetate (F9) analog was essentially inactive. A mixture of Z5-10 ∶ OAc, Z7-12 ∶ OAc, and Z9-14 ∶ OAc on a filter paper dispenser was as attractive as female gland extracts when tested in a flight tunnel. With Z5-10∶OAc omitted, the two-component mixture elicited a significantly lower male response. Four analogs, 7,7-F2, 10,10,10-F3, 7,7,8,8-F4, and F9, were added separately to the two-component mixture to replace Z5-10∶OAc. The responses elicited by the mixtures containing the 7,7-F2, 10,10,10-F3, and 7,7,8,8-F4 analogs did not differ significantly from that of the natural three-component mixture and the two-component mixture, whereas the mixture containing F9 elicited a significantly lower male response, as low as the response to the two-component mixture. In a field test the mixtures containing 10,10,10-F3 and 7,7,8,8-F4 were significantly more active than the two-component mixture, but still less active than the natural three-component mixture. It appears that field tests provided greater discrimination among pheromone analogs in assessing their behavioral activity than the flight-tunnel test did. Structure-activity analyses demonstrate the importance of the lipophilic interaction between the terminal alkyl chain and the receptor site for the activity of the stimulus. The lipophobicity of the fluorinated analogs impedes a productive receptor interaction.

Entities:  

Year:  1993        PMID: 24248519     DOI: 10.1007/BF00987479

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN: 0098-0331            Impact factor:   2.626


  15 in total

1.  Significance tests for multiple comparison of proportions, variances, and other statistics.

Authors:  T A RYAN
Journal:  Psychol Bull       Date:  1960-07       Impact factor: 17.737

2.  Determination of the vapor pressures of moth sex pheromone components by a gas chromatographic method.

Authors:  A M Olsson; J A Jönsson; B Thelin; T Liljefors
Journal:  J Chem Ecol       Date:  1983-03       Impact factor: 2.626

3.  Field attraction ofAgrotis segetum males in four european countries to mixtures containing three homologous acetates.

Authors:  H Arn; P Esbjerg; R Bues; M Tóth; G Szöcs; P Guerin; S Rauscher
Journal:  J Chem Ecol       Date:  1983-02       Impact factor: 2.626

4.  Sex pheromone components of the turnip moth,Agrotis segetum : Chemical identification, electrophysiological evaluation and behavioral activity.

Authors:  C Löfstedt; J N Van Der Pers; J Lofqvist; B S Lanne; M Appelgren; G Bergström; B Thelin
Journal:  J Chem Ecol       Date:  1982-10       Impact factor: 2.626

5.  Chemistry of pheromone and hormone metabolism in insects.

Authors:  G D Prestwich
Journal:  Science       Date:  1987-08-28       Impact factor: 47.728

6.  Adaptation of antennal neurons in moths is associated with cessation of pheromone-mediated upwind flight.

Authors:  T C Baker; B S Hansson; C Löfstedt; J Löfqvist
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

7.  Replacement of the terminal methyl group in a moth sex pheromone component by a halogen atom: Hydrophobicity and size effects on electrophysiological single-cell activities.

Authors:  S Jönsson; T Liljefors; B S Hansson
Journal:  J Chem Ecol       Date:  1991-07       Impact factor: 2.626

8.  Effects of double-bond configuration on interaction between a moth sex pheromone component and its receptor : A receptor-interaction model based on molecular mechanics.

Authors:  T Liljefors; M Engtsson; B S Hansson
Journal:  J Chem Ecol       Date:  1987-10       Impact factor: 2.626

9.  Fluorinated analogs of aldehyde components of boll weevil pheromone : Synthesis and biological activity.

Authors:  G D Prestwich; W C Sun; J C Dickens
Journal:  J Chem Ecol       Date:  1988-05       Impact factor: 2.626

10.  Behavior and survival of western spruce budworm,Choristoneura occidentalis Freeman, exposed to an ω-fluorinated pheromone analogue.

Authors:  J A McLean; B Morgan; J D Sweeney; L Weiler
Journal:  J Chem Ecol       Date:  1989-01       Impact factor: 2.626

View more
  5 in total

1.  Structure-activity relationship observations for European corn borer moth pheromone and fluoro analogs via computer molecular modeling.

Authors:  J D Warthen; J A Klun; M Schwarz; N Wakabayashi
Journal:  J Chem Ecol       Date:  1995-12       Impact factor: 2.626

2.  Alkyl ether and enol ether analogs of (Z)-5-decenyl acetate, a pheromone component of the turnip moth,Agrotis segetum: probing a proposed bioactive conformation for chain-elongated analogs.

Authors:  A L Gustavsson; T Liljefors; B S Hansson
Journal:  J Chem Ecol       Date:  1995-06       Impact factor: 2.626

3.  Selectively fluorinated analogs reveal differential olfactory reception and inactivation of green leaf volatiles in insects.

Authors:  J C Dickens; G D Prestwich; C S Ng; J H Visser
Journal:  J Chem Ecol       Date:  1993-09       Impact factor: 2.626

4.  Electrophysiological and field activity of halogenated analogs of (E,E)-8,10-dodecadien-1-ol, the main pheromone component, in codling moth (Cydia pomonella L.).

Authors:  P Lucas; M Renou; F Tellier; A Hammoud; H Audemard; C Descoins
Journal:  J Chem Ecol       Date:  1994-03       Impact factor: 2.626

5.  Moth responses to selectively fluorinated sex pheromone analogs.

Authors:  J A Klun; M Schwarz; N Wakabayashi; R M Waters
Journal:  J Chem Ecol       Date:  1994-10       Impact factor: 2.626

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.