5-HT4 receptor
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5-Hydroxytryptamine receptor 4 is a protein that in humans is encoded by the HTR4 gene.
Function
This gene is a member of the family of human serotonin receptors, which are G protein-coupled receptors that stimulate cAMP production in response to serotonin (5-hydroxytryptamine). The gene product is a glycosylated transmembrane protein that functions in both the peripheral and central nervous system to modulate the release of various neurotransmitters. Multiple transcript variants encoding proteins with distinct C-terminal sequences have been described, but the full-length nature of some transcript variants has not been determined.
Location
The receptor is located in the alimentary tract, urinary bladder, heart and adrenal gland as well as the central nervous system (CNS). In the CNS the receptor appears in the putamen, caudate nucleus, nucleus accumbens, globus pallidus, and substantia nigra, and to a lesser extent in the neocortex, raphe, pontine nuclei, and some areas of the thalamus. It has not been found in the cerebellum.
Isoforms
Internalization is isoform-specific.
Ligands
Several drugs that act as 5-HT4 selective agonists have recently been introduced into use in both scientific research and clinical medicine. Some drugs that act as 5-HT4 agonists are also active as 5-HT3 antagonists, such as metoclopramide, mosapride, renzapride, and zacopride, and so these compounds cannot be considered highly selective. Research in this area is ongoing. Amongst these agonists prucalopride has >150-fold higher affinity for 5-HT4 receptors than for other receptors.
SB-207,145 radiolabeled with carbon-11 is used as a radioligand for 5-HT4 in positron emission tomography studies in pigs and humans.
Agonists
- Cisapride
- Felcisetrag
- Metoclopramide
- Mosapride
- Naronapride
- Prucalopride
- Renzapride
- Sulpiride
- Tegaserod
- Tropisetron– partial agonist
- Usmarapride (SUVN-D4010) – partial agonist
- Zacopride
- BIMU-8
- CJ-033,466– partial agonist
- ML-10302
- RS-67506
- RS-67333– partial agonist
- SL65.0155– partial agonist
Antagonists
- L-lysine
- Piboserod
- GR-113,808 (1-methyl-1H-indole-3-carboxylic acid, [1-[2-[(methylsulfonyl)amino]ethyl]-4-piperidinyl]methyl ester)
- GR-125,487
- RS-39604 (1-[4-Amino-5-chloro-2-(3,5-dimethoxyphenyl)methyloxy]-3-[1-[2-methylsulphonylamino]piperidin-4-yl]propan-1-one)
- SB-203,186
- SB-204,070
- ([Methoxy-11C]1-butylpiperidin-4-yl)methyl 4-amino-3-methoxybenzoate
- Chamomile (ethanol extract)
See also
Further reading
External links
- . IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. Archived from on 5 June 2016.
- Humangenome location andgene details page in theUCSC Genome Browser.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.