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The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Transient receptor potential channels: targeting pain at the source

Open access
Patapoutian, Ardem, Tate, Simon, Woolf, Clifford J.·2009·Nature Reviews Drug Discovery

Abstract

Pain results from the complex processing of neural signals at different levels of the central nervous system, with each signal potentially offering multiple opportunities for pharmacological intervention. A logical strategy for developing novel analgesics is to target the beginning of the pain pathway, and aim potential treatments directly at the nociceptors — the high-threshold primary sensory neurons that detect noxious stimuli. The largest group of receptors that function as noxious stimuli detectors in nociceptors is the transient receptor potential (TRP) channel family. This Review highlights evidence supporting particular TRP channels as targets for analgesics, indicates the likely efficacy profiles of TRP-channel-acting drugs, and discusses the development pathways needed to test candidates as analgesics in humans.

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Crossref · 10.1038/nrd2757

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Metadata

Authors
Patapoutian, A., Tate, S., & Woolf, C. J.
Venue
Nature Reviews Drug Discovery
Published
2009-01
Volume
8
Issue
1
Pages
55-68
ISSN
  • 1474-1776 (ISSN-L)
  • 1474-1784
OpenAlex
W1996634599
Cited by
646
References
4
FWCI
2.86
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Transient receptor potential channels: targeting pain at the source. https://app.cochat.ai/papers/10.1038/nrd2757
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Patapoutian, A., Tate, S., & Woolf, C. J. (2009). Transient receptor potential channels: targeting pain at the source. Nature Reviews Drug Discovery. https://doi.org/10.1038/nrd2757

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.