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

Author:

Andrade RodrigoORCID,Barnes Nicholas M.,Baxter Gordon,Bockaert Joel,Branchek Theresa,Butler Amy,Cohen Marlene L.,Dumuis Aline,Eglen Richard M.,Göthert Manfred,Hamblin Mark,Hamon Michel,Hartig Paul R.,Hen René,Hensler Julie,Herrick-Davis Katharine,Hills Rebecca,Hoyer DanielORCID,Humphrey Patrick P. A.,Latté Klaus Peter,Maroteaux LucORCID,Martin Graeme R.,Middlemiss Derek N.,Mylecharane Ewan,Neumaier John,Peroutka Stephen J.,Peters John A.ORCID,Roth Bryan,Saxena Pramod R.,Sharp Trevor,Sleight Andrew,Villalon Carlos M.,Yocca Frank

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]).

Publisher

Edinburgh University Library

Subject

General Medicine

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