The role of spinal cord vanilloid (TRPV1) receptors in pain modulation
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
18481913
DOI
10.33549/physiolres.931601
PII: 1601
Knihovny.cz E-resources
- MeSH
- Pain physiopathology MeSH
- Capsaicin pharmacology MeSH
- TRPV Cation Channels metabolism MeSH
- Humans MeSH
- Spinal Cord metabolism MeSH
- Synaptic Transmission physiology MeSH
- Ganglia, Spinal metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Capsaicin MeSH
- TRPV Cation Channels MeSH
- TRPV1 receptor MeSH Browser
Transient receptor potential vanilloid 1 (TRPV1) receptor is a nonselective cation channel activated by capsaicin, a pungent substance from chili peppers. It is considered to act as an integrator of various physical and chemical nociceptive stimuli, as it can be gated by noxious heat (>43 oC), low pH (protons) and also by recently described endogenous lipids. The structure and function of TRPV1 receptors was vigorously studied, especially since its cloning in 1997. However, most of the research was pointed towards the role of TRPV1 receptors in the peripheral tissues. Mounting evidence now suggests that TRPV1 receptors on the central branches of dorsal root ganglion neurons in the spinal cord may play an important role in modulation of pain and nociceptive transmission. The aim of this short review was to summarize the knowledge about TRPV1 receptors in the spinal cord dorsal horn, preferentially from morphological and electrophysiological studies on spinal cord slices and from in vivo experiments.
References provided by Crossref.org
TRPV1 antagonist attenuates postoperative hypersensitivity by central and peripheral mechanisms