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 AbstractSex and the single neuron: pheromones excite    Next AbstractRelaxed selective pressure on an essential component of pheromone transduction in primate evolution »

J Physiol


Title:Regulation by voltage and adenine nucleotides of a Ca2+-activated cation channel from hamster vomeronasal sensory neurons
Author(s):Liman ER;
Address:"Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA. Liman@USC.edu"
Journal Title:J Physiol
Year:2003
Volume:20030314
Issue:Pt 3
Page Number:777 - 787
DOI: 10.1113/jphysiol.2002.037119
ISSN/ISBN:0022-3751 (Print) 1469-7793 (Electronic) 0022-3751 (Linking)
Abstract:"Bipolar sensory neurons within the vomeronasal organ (VNO) are thought to mediate the detection of pheromones in vertebrates. In the mouse, VNO neurons respond to pheromones with a rise in intracellular Ca2+ that accompanies a depolarization of the cell. Transduction of the pheromone appears to occur through the activation of a phosphatidylinositol signalling pathway, but the ion channels that respond to this signalling pathway have not been identified. In this report patch-clamp recording from hamster vomeronasal sensory neurons was used to identify second-messenger-gated channels that might play a role in transduction. The results demonstrate that VNO neurons show abundant expression of a Ca2+-activated non-selective (CaNS) cation channel. The CaNS channel does not discriminate between Na+ and K+ and has a slope conductance of 22 pS. Half-activation of the channel occurs at a Ca2+ concentration of 0.5 mM (at -80 mV). The probability of opening (Po) of the channel is further augmented at positive potentials, and shows an e-fold voltage dependence per 37 mV. The channel exhibits rapid rundown following patch excision with Po decreasing from near 1.0 to near 0. The adenine nucleotides ATP and cAMP block the channel with an apparent affinity of 3 and 42 microM, respectively (-80 mV). Both the activation of the channel by Ca2+ and the block of the channel by adenine nucleotides show a mild voltage dependence, which can be accounted for by the voltage dependence of Po. The properties of this channel make it a candidate to either directly mediate vomeronasal sensory transduction, or to amplify the primary sensory response"
Keywords:"Animals Calcium/*physiology Cricetinae Dendrites/physiology Ion Channel Gating/physiology Ion Channels/*physiology Membrane Potentials/physiology Mice Neurons, Afferent/*physiology Patch-Clamp Techniques Second Messenger Systems/physiology Vomeronasal Org;"
Notes:"MedlineLiman, Emily R eng DC04213/DC/NIDCD NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. England 2003/03/18 J Physiol. 2003 May 1; 548(Pt 3):777-87. doi: 10.1113/jphysiol.2002.037119. Epub 2003 Mar 14"

 
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 16-11-2024