|5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled|
|Symbols||; 5-HT6; 5-HT6R|
|External IDs||IUPHAR: ChEMBL: GeneCards:|
|RNA expression pattern|
The 5-HT6 receptor is a subtype of 5-HT receptor that binds the endogenous neurotransmitter serotonin (5-hydroxytryptamine, 5-HT). It is a G protein-coupled receptor (GPCR) that is coupled to Gs and mediates excitatory neurotransmission. HTR6 denotes the human gene encoding for the receptor.
- Distribution 1
- Function 2
- Full agonists 3.1
- Partial Agonists 3.2
- Antagonists 3.3
- Genetics 4
- See also 5
- References 6
- Further reading 7
- External links 8
The 5-HT6 receptor is expressed almost exclusively in the brain. It is distributed in various areas including, but not limited to, the olfactory tubercle, cerebral cortex (frontal and entorhinal regions), nucleus accumbens, striatum, caudate nucleus, hippocampus, and the molecular layer of the cerebellum. Based on its abundance in extrapyramidal, limbic, and cortical regions it can be suggested that the 5-HT6 receptor plays a role in functions like motor control, emotionality, cognition, and memory.
Blockade of central 5-HT6 receptors has been shown to increase glutamatergic and cholinergic neurotransmission in various brain areas, whereas activation enhances GABAergic signaling in a widespread manner. Antagonism of 5-HT6 receptors also facilitates dopamine and norepinephrine release in the frontal cortex, while stimulation has the opposite effect.
Despite the 5-HT6 receptor having a functionally excitatory action, it is largely co-localized with GABAergic neurons and therefore produces an overall inhibition of brain activity. In parallel with this, 5-HT6 antagonists improve cognition, learning, and memory, and agents such as latrepirdine, Lu AE58054, and SB-742,457 are being developed as novel treatments for Alzheimer's disease and other forms of dementia. 5-HT6 antagonists have also been shown to reduce appetite and produce weight loss, and as a result, PRX-07034, BVT-5,182, and BVT-74,316 are being investigated for the treatment of obesity.
Recently, the 5-HT6 agonists WAY-181,187 and WAY-208,466 have been demonstrated to be active in rodent models of depression, anxiety, and obsessive-compulsive disorder (OCD), and such agents may be useful treatments for these conditions. Additionally, it can be inferred that 5-HT6 activation likely plays a major role in the therapeutic benefits of serotonergic antidepressants like the selective serotonin reuptake inhibitors (SSRIs) and tricyclic antidepressants (TCAs).
A large number of selective 5-HT6 ligands have now been developed and this is a productive current area of research.
- EMD-386,088 - potent and selective 5HT6 agonist (EC50 1nM)
- 2-Ethyl-5-methoxy-N,N-dimethyltryptamine (EMDT)
- N1-(6-chloroimidazo[2,1-b][1,3]thiazole-5-sulfonyl)tryptamine (compound 11q)
- N-(inden-5-yl)imidazothiazole-5-sulfonamide (43): Ki = 4.5nM, EC50 = 0.9nM, Emax = 98%
- E-6837 - Full agonist at human 5-HT6 receptors
- E-6837 - partial agonist at rat 5-HT6 receptors. Orally active in rats, and caused weight loss with chronic administration
- EGIS-12233 - mixed 5-HT6 / 5-HT7 antagonist
- Latrepirdine (non-selective) and analogues
- Lu AE58054
- Atypical antipsychotics (olanzapine, asenapine, clozapine)
- WAY-255315 / SAM-315: Ki = 1.1nM, IC = 13nM
The receptor is encoded by the HTR6 gene. As the protein is a neuroreceptor it is possible that genetic variations in the gene would have an effect on brain, and research studies have investigated whether polymorphisms is associated with brain-related variables, such as neuropsychiatric disorders. For example, in 2004 one Chinese study reported an association between the C267T (rs1805054) polymorphism and Alzheimer's disease. Others have studied the polymorphism in relation to Parkinson's disease.
- 5-HT receptor
- 5-HT1 receptor
- 5-HT2 receptor
- 5-HT3 receptor
- 5-HT4 receptor
- 5-HT5 receptor
- 5-HT7 receptor
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- serotonin 6 receptor at the US National Library of Medicine Medical Subject Headings (MeSH)