Abstract

Capsaicin, the main pungent ingredient in 'hot' chilli peppers, elicits a sensation of burning pain by selectively activating sensory neurons that convey information about noxious stimuli to the central nervous system. We have used an expression cloning strategy based on calcium influx to isolate a functional cDNA encoding a capsaicin receptor from sensory neurons. This receptor is a non-selective cation channel that is structurally related to members of the TRP family of ion channels. The cloned capsaicin receptor is also activated by increases in temperature in the noxious range, suggesting that it functions as a transducer of painful thermal stimuli in vivo.

Keywords

CapsaicinChemistryIon channelReceptorTransient receptor potential channelTRPV1PharmacologyBiophysicsMedicineBiologyBiochemistry

MeSH Terms

Afferent PathwaysAmino Acid SequenceAnimalsCalciumCalcium ChannelsCapsaicinCapsicumCell DeathCell LineCloningMolecularDrosophila ProteinsElectrophysiologyHot TemperatureHumansInsect ProteinsIon Channel GatingIon ChannelsMolecular Sequence DataNeuronsAfferentNeurotoxinsNociceptorsPlantsMedicinalProtonsReceptorsDrugSequence HomologyAmino AcidTransient Receptor Potential ChannelsXenopus

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Publication Info

Year
1997
Type
article
Volume
389
Issue
6653
Pages
816-824
Citations
8889
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

8889
OpenAlex
587
Influential
7577
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Cite This

Michael J. Caterina, Mark Schumacher, Makoto Tominaga et al. (1997). The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature , 389 (6653) , 816-824. https://doi.org/10.1038/39807

Identifiers

DOI
10.1038/39807
PMID
9349813

Data Quality

Data completeness: 86%