Abstract
Transient receptor potential (TRP) is a large superfamily of cation channels comprising 28 members in mammals. TRP channels are ubiquitously expressed in human tissues, including the cardiovascular system where they have been associated with a number of physiological functions, such as proliferation, contraction, and migration. TRP channels comprise six large families of cation channels: TRPC, TRPM, TRPV, TRPP, TRPA, and TRPML with diverse ion selectivities and modes of activation. Depending on the isoform considered, activation of TRP channels can cause entry of Ca2+, Na+, or Mg2+ into cells. TRP channels have recently emerged as attractive drug targets for treatment of cardiovascular diseases since their expression and/or activation was shown to be disturbed in certain pathophysiological conditions, such as cardiac hypertrophy and hypertension. In this short review, we will summarize data on the expression of TRP channels in the three major cell types of the cardiovascular system: cardiomyocytes, endothelial cells, and smooth muscle cells and will review evidence for the involvement of TRP channels in mediating cardiovascular disease.
| Original language | English (US) |
|---|---|
| Title of host publication | TRP Channels in Drug Discovery |
| Subtitle of host publication | Volume II |
| Editors | Arpad Szallasi, Tamas Biro |
| Pages | 3-40 |
| Number of pages | 38 |
| DOIs | |
| State | Published - 2012 |
Publication series
| Name | Methods in Pharmacology and Toxicology |
|---|---|
| ISSN (Print) | 1557-2153 |
| ISSN (Electronic) | 1940-6053 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- General Pharmacology, Toxicology and Pharmaceutics
- Pharmacology (medical)
- Molecular Medicine
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