Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1998-10-28
pubmed:abstractText
Capsaicin, the main pungent ingredient in "hot" chili peppers, elicits buming pain by activating specific (vanilloid) receptors on sensory nerve endings. The cloned vanilloid receptor (VR1) is a cation channel that is also activated by noxious heat. Here, analysis of heat-evoked single channel currents in excised membrane patches suggests that heat gates VR1 directly. We also show that protons decrease the temperature threshold for VR1 activation such that even moderately acidic conditions (pH < or = 5.9) activate VR1 at room temperature. VR1 can therefore be viewed as a molecular integrator of chemical and physical stimuli that elicit pain. Immunocytochemical analysis indicates that the receptor is located in a neurochemically heterogeneous population of small diameter primary afferent fibers. A role for VR1 in injury-induced hypersensitivity at the level of the sensory neuron is presented.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0896-6273
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
531-43
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9768840-Afferent Pathways, pubmed-meshheading:9768840-Amino Acid Sequence, pubmed-meshheading:9768840-Animals, pubmed-meshheading:9768840-Capsaicin, pubmed-meshheading:9768840-Cell Line, pubmed-meshheading:9768840-Cloning, Molecular, pubmed-meshheading:9768840-Ganglia, Spinal, pubmed-meshheading:9768840-Hot Temperature, pubmed-meshheading:9768840-Humans, pubmed-meshheading:9768840-Immunohistochemistry, pubmed-meshheading:9768840-Male, pubmed-meshheading:9768840-Membrane Potentials, pubmed-meshheading:9768840-Models, Neurological, pubmed-meshheading:9768840-Molecular Sequence Data, pubmed-meshheading:9768840-Nerve Fibers, pubmed-meshheading:9768840-Neurogenic Inflammation, pubmed-meshheading:9768840-Neurons, Afferent, pubmed-meshheading:9768840-Oocytes, pubmed-meshheading:9768840-Pain, pubmed-meshheading:9768840-Patch-Clamp Techniques, pubmed-meshheading:9768840-Peptide Fragments, pubmed-meshheading:9768840-Presynaptic Terminals, pubmed-meshheading:9768840-Rats, pubmed-meshheading:9768840-Rats, Sprague-Dawley, pubmed-meshheading:9768840-Receptors, Drug, pubmed-meshheading:9768840-Recombinant Proteins, pubmed-meshheading:9768840-Sciatic Nerve, pubmed-meshheading:9768840-Spinal Cord, pubmed-meshheading:9768840-Superior Cervical Ganglion, pubmed-meshheading:9768840-Transfection, pubmed-meshheading:9768840-Xenopus laevis
pubmed:year
1998
pubmed:articleTitle
The cloned capsaicin receptor integrates multiple pain-producing stimuli.
pubmed:affiliation
Department of Cellular and Molecular Pharmacology, W.M. Keck Foundation Center for Integrative Neuroscience, University of California, San Francisco 94143, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't