5-HT2B receptor
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). 5-Hydroxytryptamine receptor 2B (5-HT2B) also known as serotonin receptor 2B is a protein that in humans is encoded by the HTR2B gene.[1][2] 5-HT2B is a member of the 5-HT2 receptor family that binds the neurotransmitter serotonin (5-hydroxytryptamine, 5-HT).
Contents
Function
The 5-HT2 receptors (of which the 5-HT2B receptor is a subtype) mediate many of the central and peripheral physiologic functions of serotonin. Cardiovascular effects include contraction of blood vessels and shape changes in platelets; central nervous system effects include neuronal sensitization to tactile stimuli and mediation of some of the effects of hallucinogenic substituted amphetamines.
The 5-HT2B receptor subtype is involved in:
- CNS: presynaptic inhibition, behavioural effects[3]
- Vascular: pulmonary vasoconstriction[4]
- Cardiac: The 5-HT2B receptor regulates cardiac structure and functions as demonstrated by the abnormal cardiac development observed in 5-HT2B receptor null mice.[5] The 5-HT2B receptor stimulation can also lead to pathological proliferation of cardiac valves fibroblasts,[6] which with chronic overstimulation of 5-HT2B can lead to a severe valvulopathy. Moreover, 5-HT2B receptors were recently shown to be overexpressed in human failing heart and antagonists of 5-HT2B receptors were uncovered to prevent both angiotensin II or beta-adrenergic agonist-induced pathological cardiac hypertrophy in mouse.[7][8][9]
- Serotonin transporter: 5-HT2B receptors regulate serotonin release via the serotonin transporter, and are important both to normal physiological regulation of serotonin levels in blood plasma,[10] and with the abnormal acute serotonin release produced by drugs such as MDMA.[3] Surprisingly however 5-HT2B receptor activation appears to be protective against the development of serotonin syndrome following elevated extracellular serotonin levels,[11] despite its role in modulating serotonin release.
Clinical significance
5-HT2B receptors have also been strongly implicated in drug-induced valvular heart disease.[12][13][14] In this context, it is generally considered to be an antitarget.
The structure of the 5-HT2B receptor was recently solved in complex with the valvulopathogenic drug ergotamine.[15]
Ligands
As of 2009, few highly selective 5-HT2B receptor ligands have been discovered, although numerous potent non-selective compounds are known, particularly agents with concomitant 5-HT2C binding. Research in this area has been limited due to the cardiotoxicity of 5-HT2B agonists, and the lack of clear therapeutic application for 5-HT2B antagonists, but there is still a need for selective ligands for scientific research.[16]
Agonists
- Selective
- BW-723C86:[17] fair functional subtype selectivity; almost full agonist. Anxiolytic in vivo.[18]
- Ro60-0175 [17] functionally selective over 5-HT2A, potent agonist at both 5-HT2B/C
- VER-3323: selective for 5-HT2B/C over 5-HT2A
- α-Methyl-5-HT - moderately selective over 5-HT2A/C
- 6-APB
- psilocin - 23x greater selectivity for human cloned 5-HT2B receptors over 5-HT2A.[19]
- Non-selective
- Guanfacine - an α2A agonist, but has 5-HT2B agonistic activity at therapeutic concentrations.[20]
- MDMA (Ecstasy)[21]
- MDA[21]
- MEM[22]
- Pergolide[23]
- Cabergoline
- Norfenfluramine[17]
- Chlorphentermine
- Aminorex
- mCPP
- Bromo-dragonfly
- DMT
- 5-MeO-DMT
- LSD-25 - About equal affinity for human cloned 5-HT2B and 5-HT2A receptors.[19]
Antagonists
- Agomelatine - primarily a melatonin Mt1/Mt2 receptor agonist, with a less potent antagonism of 5-HT2B and 5-HT2C.[24]
- Sarpogrelate: a mixed 5-HT2A/B antagonist
- Lisuride: a dopamine agonist of the ergoline class, that is also a 5-HT2B antagonist[25] and a dual 5-HT2A/C agonist[26]
- Tegaserod: primarily a 5-HT4 agonist, but also a 5-HT2B antagonist[27]
- RS-127,445:[28] high affinity; subtype selective (1000x), selective over at least eight other 5-HTR types; orally bioavailable.
- SDZ SER-082: a mixed 5-HT2B/C antagonist
- EGIS-7625: high selectivity over 5-HT2A[29]
- PRX-08066
- SB-200,646
- SB-204,741
- SB-206,553: mixed 5-HT2B/C antagonist and PAM at α7 nAChR[30]
- SB-215,505 [31]
- SB-228,357
- LY-266,097
- LY-272,015
Possible applications
5-HT2B antagonists have previously been proposed as treatment for migraine headaches, and RS-127,445 was trialled in humans up to Phase I for this indication, but development was not continued.[32] More recent research has focused on possible application of 5-HT2B antagonists as treatments for chronic heart disease.[33][34] Research claims serotonin 5-HT2B receptors have effect on liver regeneration.[35]
See also
References
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- ↑ PDB: 4IB4; Lua error in package.lua at line 80: module 'strict' not found.
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- ↑ 19.0 19.1 PDSP Ki database, University of North Carolina at Chapel Hill. http://pdsp.med.unc.edu/pdsp.php
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Further reading
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External links
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.