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 AbstractEvidence for regulation of resistance in Arabidopsis to Egyptian cotton worm by salicylic and jasmonic acid signaling pathways    Next AbstractDifferential induction of tomato foliar proteins by arthropod herbivores »

PLoS One


Title:Citral sensing by Transient [corrected] receptor potential channels in dorsal root ganglion neurons
Author(s):Stotz SC; Vriens J; Martyn D; Clardy J; Clapham DE;
Address:"Howard Hughes Medical Institute, Department of Cardiology, Children's Hospital, Boston, Massachusetts, United States of America"
Journal Title:PLoS One
Year:2008
Volume:20080507
Issue:5
Page Number:e2082 -
DOI: 10.1371/journal.pone.0002082
ISSN/ISBN:1932-6203 (Electronic) 1932-6203 (Linking)
Abstract:"Transient receptor potential (TRP) ion channels mediate key aspects of taste, smell, pain, temperature sensation, and pheromone detection. To deepen our understanding of TRP channel physiology, we require more diverse pharmacological tools. Citral, a bioactive component of lemongrass, is commonly used as a taste enhancer, as an odorant in perfumes, and as an insect repellent. Here we report that citral activates TRP channels found in sensory neurons (TRPV1 and TRPV3, TRPM8, and TRPA1), and produces long-lasting inhibition of TRPV1-3 and TRPM8, while transiently blocking TRPV4 and TRPA1. Sustained citral inhibition is independent of internal calcium concentration, but is state-dependent, developing only after TRP channel opening. Citral's actions as a partial agonist are not due to cysteine modification of the channels nor are they a consequence of citral's stereoisoforms. The isolated aldehyde and alcohol cis and trans enantiomers (neral, nerol, geranial, and geraniol) each reproduce citral's actions. In juvenile rat dorsal root ganglion neurons, prolonged citral inhibition of native TRPV1 channels enabled the separation of TRPV2 and TRPV3 currents. We find that TRPV2 and TRPV3 channels are present in a high proportion of these neurons (94% respond to 2-aminoethyldiphenyl borate), consistent with our immunolabeling experiments and previous in situ hybridization studies. The TRPV1 activation requires residues in transmembrane segments two through four of the voltage-sensor domain, a region previously implicated in capsaicin activation of TRPV1 and analogous menthol activation of TRPM8. Citral's broad spectrum and prolonged sensory inhibition may prove more useful than capsaicin for allodynia, itch, or other types of pain involving superficial sensory nerves and skin"
Keywords:"Acyclic Monoterpenes Animals Ganglia, Spinal/*physiology Kinetics Monoterpenes/*pharmacology Neurons/drug effects/*physiology Patch-Clamp Techniques Rats Stereoisomerism TRPV Cation Channels/antagonists & inhibitors/drug effects/*physiology;"
Notes:"MedlineStotz, Stephanie C Vriens, Joris Martyn, Derek Clardy, Jon Clapham, David E eng Howard Hughes Medical Institute/ Research Support, Non-U.S. Gov't 2008/05/08 PLoS One. 2008 May 7; 3(5):e2082. doi: 10.1371/journal.pone.0002082"

 
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 29-06-2024