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Pharmacology of Vanilloid Transient Receptor Potential Cation Channels

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Vriens, Joris, Appendino, Giovanni, Nilius, Bernd·2009·Molecular Pharmacology

Abstract

Depending on their primary structure, the 28 mammalian transient receptor potential (TRP) cation channels identified so far can be sorted into 6 subfamilies: TRPC (“Canonical”), TRPV (“Vanilloid”), TRPM (“Melastatin”), TRPP (“Polycystin”), TRPML (“Mucolipin”), and TRPA (“Ankyrin”). The TRPV subfamily (vanilloid receptors) comprises channels critically involved in nociception and thermosensing (TRPV1, TRPV2, TRPV3, and TRPV4), whereas TRPV5 and TRPV6 are involved in renal Ca2+ absorption/reabsorption. Apart from TRPV1, the pharmacology of these channels is still insufficiently known. Furthermore, only few small-molecule ligands for non-TRPV1 vanilloid receptors have been identified, and little is known of their endogenous ligands, resulting in a substantial “orphan” state for these channels. In this review, we summarize the pharmacological properties of members of the TRPV subfamily, highlighting the critical issues and challenges facing their “deorphanization” and clinical exploitation.

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Metadata

Authors
Vriens, J., Appendino, G., & Nilius, B.
Venue
Molecular Pharmacology
Publisher
Elsevier BV
Published
2009-06
Volume
75
Issue
6
Pages
1262-1279
ISSN
0026-895X (ISSN-L)
OpenAlex
W2123673561
Cited by
418
References
3
FWCI
13.64
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Pharmacology of Vanilloid Transient Receptor Potential Cation Channels. https://app.cochat.ai/papers/10.1124/mol.109.055624
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Vriens, J., Appendino, G., & Nilius, B. (2009). Pharmacology of Vanilloid Transient Receptor Potential Cation Channels. Molecular Pharmacology. https://doi.org/10.1124/mol.109.055624

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