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5-Hydroxytryptamine receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database

Authors :
Pramod R. Saxena
Patrick P.A. Humphrey
Joël Bockaert
Rebecca Hills
Sleight Andrew
Rodrigo Andrade
Amy S. Butler
Bryan L. Roth
Graeme R. Martin
Frank D. Yocca
Stephen J. Peroutka
Manfred Göthert
Julie Hensler
Carlos M. Villalón
Katharine Herrick-Davis
Luc Maroteaux
Richard M. Eglen
Paul R. Hartig
Nicholas M. Barnes
M. Hamon
Theresa Branchek
Aline Dumuis
Klaus Peter Latté
Mark W. Hamblin
Trevor Sharp
Ewan J. Mylecharane
John F. Neumaier
René Hen
John A. Peters
Marlene L. Cohen
Derek N. Middlemiss
Gordon Baxter
Daniel Hoyer
Source :
IUPHAR/BPS Guide to Pharmacology CITE. 2019
Publication Year :
2019
Publisher :
Edinburgh University Library, 2019.

Abstract

5-HT receptors (nomenclature as agreed by the NC-IUPHAR Subcommittee on 5-HT receptors [194] and subsequently revised [176]) are, with the exception of the ionotropic 5-HT3 class, GPCRs where the endogenous agonist is 5-hydroxytryptamine. The diversity of metabotropic 5-HT receptors is increased by alternative splicing that produces isoforms of the 5-HT2A (non-functional), 5-HT2C (non-functional), 5-HT4, 5-HT6 (non-functional) and 5-HT7 receptors. Unique amongst the GPCRs, RNA editing produces 5-HT2C receptor isoforms that differ in function, such as efficiency and specificity of coupling to Gq/11 and also pharmacology [40, 482]. Most 5-HT receptors (except 5-ht1e and 5-ht5b) play specific roles mediating functional responses in different tissues (reviewed by [463, 382]).

Details

ISSN :
26331020
Volume :
2019
Database :
OpenAIRE
Journal :
IUPHAR/BPS Guide to Pharmacology CITE
Accession number :
edsair.doi...........acc171822fcb3a73f3b0da9179a7a21b