5-HT1B receptor
5-hydroxytryptamine receptor 1B also known as the 5-HT1B receptor is a protein that in humans is encoded by the HTR1B gene. The 5-HT1B receptor is a 5-HT receptor subtype.
Tissue distribution and function
5-HT1B receptors are widely distributed throughout the central nervous system with the highest concentrations found in the frontal cortex, basal ganglia, striatum, and the hippocampus.The function of the 5-HT1B receptor differs depending upon its location. In the frontal cortex, it is believed to act as a terminal receptor inhibiting the release of dopamine. In the basal ganglia and the striatum, evidence suggests 5-HT signaling acts on an autoreceptor, inhibiting the release of serotonin and decreasing glutamatergic transmission by reducing miniature excitatory postsynaptic potential frequency, respectively. In the hippocampus, a recent study has demonstrated that activation of postsynaptic 5-HT1B heteroreceptors produces a facilitation in excitatory synaptic transmission which is altered in depression.
When the expression of 5-HT1B in human cortex was traced throughout life, significant changes during adolescence were observed, in a way that is strongly correlated with the expression of 5-HT1E.
Outside of the CNS, the 5-HT1B receptor is also expressed on the endothelium of blood vessels, particularly in the meninges. Activation of these receptors results in vasoconstriction. The high distribution of vasoconstrictive 5-HT1B and 5-HT1D receptors around the brain makes them a valuable drug target for the treatment of migraines.
Blocking 5-HT1B receptor signalling also increases the number of osteoblasts, bone mass, and the bone formation rate.
Knockout mice lacking the 5-HT1B gene have been reported to have a higher preference for alcohol, although later studies failed to replicate such abnormalities in alcohol consumption. These mice have also been reported to have a lower measure of anxiety and a higher measure of aggression.
Under basal conditions, knockout mice present with a "normal" phenotype and exhibit a sucrose preference. However, after undergoing chronic unpredictable stress treatment to induce a "depression-like" phenotype these animals do not benefit from administration of selective [serotonin reuptake inhibitor].
Activation of the serotonin 5-HT1B receptor appears to mediate the prosocial effects of entactogens acting as serotonin releasing agents like MDMA in animals. In addition, serotonin 5-HT1B receptor activation appears to mediate the locomotor hyperactivity of these agents. The serotonin 5-HT1B receptor also appears to be required for the persisting antidepressant- and anxiolytic-like effects as well as acute hypolocomotion of the serotonergic psychedelic and non-selective serotonin receptor agonist psilocybin in animals.
Ligands
Agonists
- 2ZEDMA
- 5-Carboxamidotryptamine
- 5-MAPB
- 5-MAPBT
- 6-MAPB
- 6-MAPBT
- Almotriptan
- Anpirtoline
- Avitriptan
- Batoprazine
- BK-5-MAPB
- BK-5-MAPBT
- BK-6-MAPB
- CGS-12066
- CP-93,129
- CP-94,253
- CP-122,288
- CP-135,807
- Dihydroergotamine
- Donitriptan
- Eletriptan
- Eltoprazine
- Emodin-8-glucoside
- Ergotamine
- Fluprazine
- Frovatriptan
- L-741604
- Lisuride
- mCPP
- MDMA
- Methylergometrine
- Methylone
- Methysergide
- Naratriptan
- Oxymetazoline
- Pergolide
- PGI-7043
- PZKKN-94
- Rizatriptan
- RU-24969
- -DCPT
- Serotonin
- Sumatriptan
- TFMPP
- Tryptamine psychedelics
- Zolmitriptan
Partial agonists
- Asenapine
- AZ10419369
- Bromocriptine
- Metergoline
- Naphthylpiperazine
- Vortioxetine
- Ziprasidone
Antagonists and inverse agonists
- Alprenolol
- AOP-208
- AR-A000002
- Aripiprazole
- AZD-1134
- AZD-3783
- AZ12320927
- Carteolol
- Elzasonan
- F-14258
- GR-55562
- GR-127935
- Isamoltane
- LY-393558
- Metitepine
- NAS-181
- Oxprenolol
- Penbutolol
- Propranolol
- Risperidone
- SB-216,641
- SB-224,289
- SB-236,057
- SB-245,570
- SB-616234
- SB-649,915
- Tertatolol
- Yohimbine
Negative allosteric modulators
- 5-HT-moduline
Unknown
- Dextromethorphan
Genetics
A genetic variant in the promoter region, A-161T, has been examined with respect to personality traits and showed no major effect.