Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/30301
Title: The capsaicin receptor TRPV1 is a crucial mediator of the noxious effects of mustard oil
Authors: Everaerts, Wouter
Gees, Maarten
Alpizar, Yeranddy A
Farre, Ricard
Leten, Cindy
Apetrei, Aurelia
DEWACHTER, Ilse 
van Leuven, Fred
Vennekens, Rudi
De Ridder, Dirk
Nilius, Bernd
Voets, Thomas
Talavera, Karel
Issue Date: 2011
Publisher: CELL PRESS
Source: Current biology : CB, 21 (4) , p. 316 -321
Abstract: Mustard oil (MO) is a plant-derived irritant that has been extensively used in experimental models to induce pain and inflammation. The noxious effects of MO are currently ascribed to specific activation of the cation channel TRPA1 in nociceptive neurons. In contrast to this view, we show here that the capsaicin receptor TRPV1 has a surprisingly large contribution to aversive and pain responses and visceral irritation induced by MO. Furthermore, we found that this can be explained by previously unknown properties of this compound. First, MO has a bimodal effect on TRPA1, producing current inhibition at millimolar concentrations. Second, it directly and stably activates mouse and human recombinant TRPV1, as well as TRPV1 channels in mouse sensory neurons. Finally, physiological temperatures enhance MO-induced TRPV1 stimulation. Our results refute the dogma that TRPA1 is the sole nocisensor for MO and motivate a revision of the putative roles of these channels in models of MO-induced pain and inflammation. We propose that TRPV1 has a generalized role in the detection of irritant botanical defensive traits and in the coevolution of multiple mammalian and plant species.
Keywords: Rat Urinary-Bladder;Potential Channels;Ion-Channel;Functional-Characterization;Chemical Nociception;Trpa1;Pain;Cold;Transduction;Inflammation
Document URI: http://hdl.handle.net/1942/30301
ISSN: 0960-9822
e-ISSN: 1879-0445
DOI: 10.1016/j.cub.2011.01.031
ISI #: 000287767600025
Rights: 2011 Elsevier Ltd. All rights reserved.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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