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5-HT2 receptor
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The 5-HT2 receptors are a subfamily of 5-HT receptors that bind the endogenous neurotransmitter serotonin (5-hydroxytryptamine, 5-HT).[1] The 5-HT2 subfamily consists of three G protein-coupled receptors (GPCRs) which are coupled to Gq/G11 and mediate excitatory neurotransmission,[2] including 5-HT2A, 5-HT2B, and 5-HT2C. For more information, please see the respective main articles of the individual subtypes:
See also
[edit]References
[edit]- ^ Hoyer D, Clarke DE, Fozard JR, Hartig PR, Martin GR, Mylecharane EJ, Saxena PR, Humphrey PP (1994). "International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin)". Pharmacol. Rev. 46 (2): 157–203. PMID 7938165.
- ^ Eison AS, Mullins UL (1996). "Regulation of central 5-HT2A receptors: a review of in vivo studies". Behavioural Brain Research. 73 (1–2): 177–81. doi:10.1016/0166-4328(96)00092-7. PMID 8788498.
5-HT2 receptor
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Discovery and Nomenclature
Historical Background
Early investigations into the physiological effects of serotonin (5-HT) in the 1950s revealed its potent contractile actions on smooth muscle tissues. In a seminal study, Gaddum and Hameed (1954) examined the antagonism of 5-HT-induced contractions in isolated preparations of rat uterus and guinea-pig ileum, demonstrating that certain compounds like morphine selectively blocked these responses, highlighting the receptor-mediated nature of the effects.[5] Building on this, Gaddum and Picarelli (1957) further differentiated two distinct 5-HT receptor populations in guinea-pig ileum: "D" receptors responsible for direct contractile responses (later identified as 5-HT2A) and "M" receptors mediating indirect effects via neuronal pathways (now classified as 5-HT3).[6] The development of radioligand binding assays in the 1970s enabled the direct visualization and distinction of 5-HT receptor sites in the brain. Fillion and colleagues (1976) reported the first high-affinity binding of [³H]5-HT to synaptic membranes from rat brain, characterizing these sites (subsequently termed 5-HT1) by their nanomolar affinity for 5-HT and sensitivity to agonists like lysergic acid diethylamide (LSD).[7] These findings laid the groundwork for identifying heterogeneous 5-HT populations, as [³H]5-HT primarily labeled high-affinity sites while other ligands revealed additional subtypes. A pivotal advancement occurred in 1979 when Peroutka and Snyder utilized [³H]spiperone—a selective antagonist initially developed for dopamine receptors—as a radioligand to detect a novel class of 5-HT binding sites in rat brain membranes.[8] These sites exhibited lower affinity for 5-HT compared to 5-HT1 but high affinity for spiperone and hallucinogenic agents like LSD, leading to the formal proposal of 5-HT2 receptors based on this pharmacological profile.[8] Follow-up studies in 1984 reinforced the link between 5-HT2 sites and hallucinogen action through binding assays with phenethylamine derivatives, confirming their role in mediating psychoactive effects.[9] The molecular era began in the late 1980s with the cloning of 5-HT2 receptor subtypes. In 1988, Julius et al. isolated and functionally expressed a cDNA encoding the rat 5-HT1C receptor (later redesignated as 5-HT2C in the 1990s) from choroid plexus tissue, representing the first molecularly identified member of the 5-HT2 family and revealing its G-protein-coupled structure.[10] This breakthrough facilitated subsequent cloning of the classical 5-HT2A receptor in 1988, solidifying the genetic and structural basis for subtype classification.[11]Classification and Subtypes
The 5-HT2 receptors constitute one subfamily within the broader superfamily of serotonin (5-HT) receptors, which encompasses seven distinct families (5-HT1 through 5-HT7) comprising a total of 14 pharmacologically defined subtypes, all classified as class A G protein-coupled receptors (GPCRs) belonging to the rhodopsin-like family.[12] This subfamily is distinguished by its members' primary coupling to Gq/11 proteins, leading to activation of phospholipase C and subsequent phosphoinositide hydrolysis, though subtypes exhibit nuanced differences in ligand binding and functional selectivity.[2] The 5-HT2 subfamily includes three main subtypes: 5-HT2A, 5-HT2B, and 5-HT2C, each encoded by distinct genes—HTR2A (chromosome 13q14.2), HTR2B (chromosome 2q37.1), and HTR2C (chromosome Xq23), respectively.[3] The 5-HT2A receptor, encoded by HTR2A, displays high affinity for psychedelic agonists such as lysergic acid diethylamide (LSD) and (±)-2,5-dimethoxy-4-iodoamphetamine (DOI), with Ki values typically below 10 nM for DOI, making it a primary mediator of hallucinogenic effects.[12] In contrast, the 5-HT2B receptor, encoded by HTR2B, is implicated in cardiac pathologies, as chronic agonism (e.g., by fenfluramine metabolites) promotes valvular fibrosis through sustained mitogenic signaling in heart valve interstitial cells.[13] The 5-HT2C receptor, encoded by HTR2C, undergoes extensive post-transcriptional RNA editing at five adenosine sites (A–E) in exon 5, generating up to 32 mRNA isoforms and 24 protein variants that modulate G-protein coupling efficacy and desensitization, thereby fine-tuning signaling responses.[14] Pharmacological classification of these subtypes relies on differential ligand affinities, particularly for agonists like DOI (high potency at all three, but with subtype-specific functional outcomes) and antagonists such as ketanserin, which exhibits nanomolar affinity at 5-HT2A (Ki ≈ 1–2 nM) but reduced selectivity (10- to 100-fold lower at 5-HT2B and 5-HT2C).[12] These criteria, established through radioligand binding and functional assays, enable subtype discrimination despite overlapping profiles, with additional tools like SB 204741 showing modest selectivity for 5-HT2B.[15] Evolutionarily, the 5-HT2 subfamily demonstrates high conservation across vertebrates, with the HTR2B gene likely representing the ancestral form, nested within an intron of the PSMD1 gene—a genomic arrangement tracing back over 800 million years to pre-vertebrate ancestors like Ciona intestinalis.[16] Duplications yielded HTR2A and HTR2C in tetrapods, though teleost fish exhibit five Htr2 paralogs due to whole-genome duplication; notable species differences include higher rodent 5-HT2A expression in cortex compared to humans, influencing preclinical modeling.[16]Molecular Structure
Gene Organization
The 5-HT2 receptor family is encoded by three distinct genes in humans: HTR2A, HTR2B, and HTR2C, each exhibiting unique genomic architectures that contribute to their subtype-specific expression and function. The HTR2A gene is located on chromosome 13q14.2, spanning approximately 66 kb.[17] The HTR2B gene resides on chromosome 2q37.1, covering about 17 kb.[18] In contrast, the HTR2C gene is positioned on the X chromosome at Xq24, extending over roughly 326 kb, which reflects its more complex regulatory landscape.[19] Regarding exon-intron organization, the HTR2A gene consists of three exons interrupted by two introns, with the coding sequence primarily distributed across these exons to encode the 471-amino-acid receptor protein.[20] The HTR2B gene features four exons and three introns, where the first exon is non-coding and the subsequent exons encode the functional domains, including the seven transmembrane regions characteristic of G-protein-coupled receptors.[18] The HTR2C gene has seven exons, with exons 4 through 7 containing the open reading frame; notably, it includes extensive post-transcriptional editing machinery, where ADAR enzymes target five adenosine residues (sites A-E) in exon 5 (forming a stem-loop structure in the pre-mRNA), leading to up to 24 isoforms that modulate receptor signaling.[21][14] Promoter regions of these genes harbor key regulatory elements that influence transcription. For HTR2A, the promoter contains binding sites for transcription factors such as Sp1 at CpG island -1224, which facilitates basal expression and is sensitive to methylation changes.[22] Genetic variations, including single nucleotide polymorphisms (SNPs), further shape receptor function; for instance, the rs6311 (-1438G/A) SNP in the HTR2A promoter alters transcription factor binding and is associated with increased receptor binding density for the A allele.[23] Across mammalian species, the 5-HT2 receptor genes display high sequence conservation, with orthologs sharing over 90% identity in transmembrane domains critical for ligand binding and signaling, underscoring their evolutionary preservation in serotonin-mediated pathways.[3]| Gene | Chromosomal Location | Exon Count | Key Features |
|---|---|---|---|
| HTR2A | 13q14.2 | 3 | Promoter SNP rs6311 affects density; Sp1 binding site |
| HTR2B | 2q37.1 | 4 | Nested within PSMD1 intron; high TM conservation |
| HTR2C | Xq24 | 7 | RNA editing in exon 5; longest span (~326 kb) |
Protein Topology and Ligand Binding
The 5-HT2 receptors belong to the class A subfamily of G protein-coupled receptors (GPCRs), featuring a characteristic topology with seven transmembrane-spanning α-helices (7TM), an extracellular amino (N)-terminus, and an intracellular carboxyl (C)-terminus.[24] This architecture positions the ligand-binding site within the helical bundle, while the C-terminus facilitates interactions with intracellular signaling partners.[25] The orthosteric binding pocket of 5-HT2 receptors is primarily formed by residues in transmembrane helices TM3, TM5, TM6, and TM7, enabling the endogenous agonist serotonin (5-HT) to access the core of the receptor.[24] Allosteric modulation occurs at sites involving the extracellular loop 2 (ECL2), which exhibits subtype-specific variations in length and composition that influence ligand entry and selectivity.[24] For instance, ECL2 in 5-HT2B is notably longer than in 5-HT2A or 5-HT2C, contributing to differences in ligand residence time.[26] Subtype-specific structural distinctions are evident in the binding cleft, particularly for the 5-HT2A receptor, which accommodates larger psychedelic ligands like LSD through an extended binding pocket (EBP) adjacent to the orthosteric site.[27] Cryo-electron microscopy (cryo-EM) structures from the early 2020s, such as the 5-HT2A-psilocin complex (PDB: 7WC5), highlight how the EBP allows flexible binding modes for tryptamine derivatives, with the ligand's amine group forming ionic interactions with Asp3.32.[28] In contrast, 5-HT2C structures (e.g., PDB: 6BQG with ergotamine) reveal a more constrained pocket due to residues like Gly5.42, enhancing selectivity for certain antagonists over 5-HT2A.[26] Recent 2025 cryo-EM studies have further elucidated psychedelic binding, including structures of 5-HT2AR with DMT (EMD: 43802) and other ligands, revealing additional details on selectivity and conformational dynamics.[29][30] Key ligand interactions involve conserved residues, including hydrogen bonding between the ligand's amine and Ser3.36 in TM3, which stabilizes primary amine agonists like serotonin, while steric hindrance from alkyl substitutions reduces affinity for tertiary amines.[31] The Trp6.48 residue in TM6 acts as a molecular toggle switch, rotating upon agonist binding to facilitate receptor activation; in 5-HT2A, it interacts with the indole ring of psychedelics via π-π stacking, as seen in LSD-bound structures (PDB: 7WC6).[24] These interactions, denoted using Ballesteros-Weinstein numbering, underscore the pocket's role in subtype pharmacology.[24] Evidence indicates that 5-HT2 receptors form homo- and heterodimers, with 5-HT2A/5-HT2C heterodimers driven by the 5-HT2C protomer and influencing receptor trafficking and surface expression in co-expressing cells.[32] Such dimerization may alter ligand access and G protein coupling asymmetry, though surface levels remain largely unchanged in heterologous systems.[32]Signal Transduction
G-Protein Coupling
The 5-HT2 receptors, comprising the 5-HT2A, 5-HT2B, and 5-HT2C subtypes, primarily couple to the Gq/11 family of heterotrimeric G-proteins upon activation. This coupling initiates intracellular signaling by promoting the dissociation of the Gαq/11 subunit from the Gβγ complex, with both components contributing to downstream cellular responses. Agonist binding, such as by the endogenous ligand serotonin (5-hydroxytryptamine), stabilizes an active receptor conformation that facilitates the exchange of GDP for GTP on the Gα subunit, enabling G-protein activation. This mechanism is conserved across Gq/11-coupled GPCRs, including the 5-HT2 family, and has been structurally elucidated through cryo-EM studies of agonist-bound 5-HT2A in complex with Gq.[33] Subtype-specific variations exist in G-protein coupling preferences. All three 5-HT2 subtypes robustly couple to Gq/11, as demonstrated in recombinant systems where serotonin elicits Gq-mediated calcium mobilization with pEC50 values of 7.62 (EC50 ≈ 24 nM) at 5-HT2A, 8.92 (EC50 ≈ 1.2 nM) at 5-HT2B, and 8.35 (EC50 ≈ 4.5 nM) at 5-HT2C. Similarly, the 5-HT2C subtype shows secondary Gi/o coupling alongside its primary Gq/11 interaction, potentially influencing isoform-specific signaling due to RNA editing. These quantitative potencies for serotonin activation fall within the low nanomolar range, underscoring the receptor's high sensitivity to physiological ligand concentrations.[34][35][36] In addition to G-protein pathways, 5-HT2 receptors interact with β-arrestins for regulatory functions like desensitization and internalization. Agonist-induced conformational changes promote β-arrestin recruitment, particularly at the 5-HT2A subtype, where biased agonism allows certain ligands to preferentially engage either Gq/11 or β-arrestin signaling. Recent cryo-EM structures (as of 2025) of 5-HT2A with psychedelics reveal structural diversity in active states that underpin this pathway selectivity.[30] For instance, classic agonists like serotonin activate both pathways comparably (Emax ≈ 100% for each), while psychedelics such as DOI show balanced efficacy but can be tuned for bias through structural modifications. This arrestin interaction follows G-protein activation and helps terminate signaling, with 5-HT2A demonstrating ligand-specific recruitment profiles in bioluminescence resonance energy transfer (BRET) assays.[37][3]Downstream Effector Pathways
The 5-HT2 receptor family, comprising the 5-HT2A, 5-HT2B, and 5-HT2C subtypes, primarily signals through Gq/11 proteins to activate phospholipase C (PLC), initiating the canonical phosphoinositide pathway. Upon receptor activation, Gq/11 stimulates PLC-β isoforms, which hydrolyze phosphatidylinositol 4,5-bisphosphate (PIP2) into inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG): IP3 binds to receptors on the endoplasmic reticulum, releasing intracellular Ca²⁺ stores, while DAG recruits and activates protein kinase C (PKC) isoforms, which phosphorylate downstream targets to modulate cellular responses such as contraction and secretion.[3][38] In addition to the PLC pathway, 5-HT2 receptors engage other effectors, including phospholipase A2 (PLA2), which generates arachidonic acid and its metabolites to influence inflammation and ion channel activity, particularly in 5-HT2A- and 5-HT2C-expressing cells. The mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) cascade is also activated, often via Gβγ subunits or transactivation of receptor tyrosine kinases, promoting cell proliferation and differentiation in various tissues.[3][38] Subtype-specific variations exist in these pathways; for instance, the 5-HT2C receptor activates the phosphatidylinositol 3-kinase (PI3K)/Akt pathway, contributing to neuronal survival and anti-apoptotic effects. Non-canonical β-arrestin signaling, prominent across subtypes but especially in 5-HT2A and 5-HT2C, scaffolds MAPK components to drive ERK phosphorylation independently of G proteins, influencing gene transcription via nuclear translocation.[38] Feedback mechanisms regulate these cascades to prevent overstimulation, primarily through desensitization involving G protein-coupled receptor kinase (GRK)-mediated phosphorylation of the receptor's C-terminal tail, which recruits β-arrestins to uncouple Gq/11 and promote clathrin-mediated internalization. Internalized receptors may recycle or degrade, attenuating signaling for hours, with GRK2 particularly implicated in 5-HT2A and 5-HT2B subtypes.[39]Expression and Distribution
Central Nervous System
The 5-HT2 receptors, particularly the 5-HT2A subtype, exhibit prominent expression in the central nervous system, with high densities observed in cortical regions. Autoradiographic studies have revealed substantial binding of 5-HT2A receptors in the neocortex, underscoring their abundance in this area.[40] Within the cortex, 5-HT2A receptors are predominantly localized to pyramidal neurons, especially in the prefrontal cortex, where they display layer-specific distribution, including a strong presence overlaying layer Va.[41] This localization positions 5-HT2A receptors to modulate cortical excitability and integration of sensory and cognitive signals.[42] In contrast, the 5-HT2C subtype shows distinct regional patterns, with the highest densities in the choroid plexus, where it influences cerebrospinal fluid production, and notable expression in the substantia nigra, particularly the pars reticulata.[43][44] The 5-HT2B subtype maintains minimal expression throughout the brain, including low but detectable levels in serotonergic neurons of the raphe nuclei, with low mRNA levels detected in both rodent and human tissues, limiting its role in central neural processes.[45][46] At the cellular level, 5-HT2 receptors are primarily postsynaptic on glutamatergic neurons, including pyramidal cells in cortical layers, where they enhance excitatory transmission.[47] Additionally, they function as presynaptic autoreceptors in the raphe nuclei, contributing to the regulation of serotonergic neuron firing.[48] Expression of 5-HT2A receptors undergoes dynamic changes during development, with upregulation observed during adolescence in cortical regions, potentially shaping maturational processes in neural circuitry.[49]Peripheral Tissues
The 5-HT2B receptor exhibits prominent expression in several peripheral tissues, particularly in the cardiovascular system and gastrointestinal tract. In the heart, it is localized to cardiomyocytes, cardiac fibroblasts, and valvular tissues, with detection confirmed through RT-PCR and binding studies in both embryonic and adult stages, including in humans.[50] In the gut, 5-HT2B receptors are expressed in smooth muscle cells, notably in the stomach fundus, contributing to its distribution across species including rat, mouse, and human.[50] The 5-HT2A receptor is widely distributed in peripheral vascular and hematopoietic elements. It is prominently expressed on platelets, where it facilitates serotonin-mediated responses, as evidenced by functional and binding assays in human samples.[51] In vascular endothelium and smooth muscle, 5-HT2A receptors are detected via RT-PCR and pharmacological studies, with expression also noted in bronchial smooth muscle and the lung.[52][53] The 5-HT2C receptor shows more restricted peripheral localization compared to its central abundance. It is expressed in white adipose tissue, as identified through qPCR in mouse models linking it to adiposity regulation, and in pancreatic islets, where upregulated mRNA levels have been observed in high-fat diet conditions via RT-PCR.[35][54] Species-specific variations are notable for the 5-HT2B receptor, with higher peripheral expression in rodents than in humans.[15]Physiological Functions
Role in Neural Signaling
The 5-HT2 receptors, particularly the 5-HT2A and 5-HT2C subtypes, play pivotal roles in modulating neural signaling within the central nervous system by influencing neurotransmitter release and neuronal excitability. These Gq-coupled receptors are primarily expressed on postsynaptic sites in cortical and subcortical regions, where they integrate serotonergic inputs to fine-tune excitatory and inhibitory transmission. Activation of 5-HT2A receptors on cortical pyramidal neurons enhances glutamatergic signaling, thereby promoting neuronal excitation essential for cognitive processes.[55] In the prefrontal cortex, 5-HT2A receptors located on layer V pyramidal neurons facilitate the modulation of glutamate release, leading to increased asynchronous excitatory postsynaptic currents (EPSCs) that amplify excitatory drive. This mechanism involves presynaptic enhancement of glutamate efflux, which heightens overall cortical excitability without altering synchronous release. Electrophysiologically, agonists such as serotonin or DOI induce a slow depolarization in these layer V neurons, generating excitatory postsynaptic potentials (EPSPs) of approximately 5-10 mV, which can transition to tonic firing and support network synchronization.[56][57][58] The 5-HT2C receptors exert inhibitory effects on dopaminergic transmission in the nigrostriatal pathway, where their activation on striatal GABAergic interneurons suppresses dopamine release from substantia nigra pars compacta terminals, thereby constraining reward-related signaling. This tonic inhibition helps regulate motor control and motivational behaviors by dampening excessive dopaminergic activity in striatal circuits.[59][60] In the hypothalamus, 5-HT2C receptors on pro-opiomelanocortin (POMC) neurons mediate serotonin's anorexigenic effects, promoting satiety and reducing food intake through downstream activation of melanocortin pathways. This central mechanism is critical for appetite control and energy homeostasis.[61] Circuit-specific activation of 5-HT2A receptors contributes to hallucinogenic effects by altering connectivity in the default mode network (DMN), a key system for self-referential processing and introspection; psychedelics like LSD, acting as 5-HT2A agonists, disrupt DMN integrity, reducing within-network coherence and promoting ego-dissolution experiences. Additionally, 5-HT2 receptors integrate with glutamatergic systems through crosstalk with NMDA receptors, where 5-HT2A signaling counteracts 5-HT1A-mediated suppression of NMDA currents, facilitating NMDA-dependent synaptic plasticity in cortical circuits. This interaction supports long-term potentiation and structural remodeling of dendritic spines, underpinning adaptive neural responses.[62][63][64][65]Peripheral Physiological Effects
The 5-HT2A receptor subtype plays a prominent role in regulating vascular tone in peripheral arteries, particularly mediating serotonin-induced vasoconstriction in coronary vessels. Activation of 5-HT2A receptors on vascular smooth muscle cells leads to contraction, contributing to increased vascular resistance and potential coronary artery spasms.[66] This effect is evident in isolated human coronary arteries, where 5-HT elicits concentration-dependent vasoconstriction primarily through 5-HT2A signaling, with partial contributions from other subtypes under certain conditions.[67] In the gastrointestinal tract, 5-HT2B receptors are key mediators of smooth muscle contraction, influencing motility in the colon and other segments. Stimulation of 5-HT2B receptors on intestinal smooth muscle cells promotes excitatory responses, enhancing peristalsis and potentially contributing to conditions like irritable bowel syndrome through heightened sensitivity.[68] These receptors are expressed in both smooth muscle and enteric neurons, where they facilitate 5-HT-induced contractions in human colonic tissue, distinct from relaxant effects mediated by other 5-HT subtypes.[69] Platelet aggregation is augmented by 5-HT2A receptor activation, which induces shape changes and promotes the release of additional serotonin from dense granules, amplifying thrombus formation. This process occurs via G-protein-coupled signaling in platelets, leading to cytoskeletal reorganization and enhanced aggregation under high shear conditions.[70] In damaged vessels, released 5-HT acts in an autocrine manner on platelet 5-HT2A receptors to sustain activation and contribute to occlusive events.[71] Endocrine functions involving 5-HT2 receptors extend to adipose tissue, where 5-HT2C receptors in adipocytes interact with leptin signaling to modulate appetite control peripherally. Elevated leptin levels, as seen in certain obesity models, suppress 5-HT2C receptor expression in white adipose tissue, potentially disrupting metabolic homeostasis and feeding regulation.[72] This peripheral crosstalk supports leptin's role in energy balance by influencing adipocyte responsiveness to serotonergic inputs. In vitro assays demonstrate the potency of 5-HT in eliciting contractions via 5-HT2 receptors, with representative EC50 values around 10 μM in aortic smooth muscle preparations, highlighting the receptor's sensitivity in vascular tissue.[73]Pharmacology
Endogenous and Synthetic Ligands
The 5-HT2 receptors (subtypes 5-HT2A, 5-HT2B, and 5-HT2C) are primarily activated by the endogenous agonist serotonin (5-HT), which binds as a full agonist with moderate affinity across all three subtypes, exhibiting pKi values of 6.0–8.4 at human 5-HT2A, 7.9–8.4 at human 5-HT2B, and 6.8–8.6 at human 5-HT2C receptors.[74][36][35] Trace amines such as tryptamine also interact as weak agonists, with pKi values of 5.5–7.6 at human 5-HT2A receptors, though their physiological relevance remains limited compared to 5-HT.[74] A range of synthetic ligands has been developed to probe 5-HT2 receptor function, including subtype-selective agonists, antagonists, and inverse agonists that target the orthosteric binding site. Representative agonists include α-methyl-5-HT, a non-selective full agonist with comparable affinity across the subtypes (pKi 7.8 at human 5-HT2A), and DOI (2,5-dimethoxy-4-iodoamphetamine), which exhibits comparable affinity across subtypes (pKi 7.4–9.2 at human 5-HT2A, 7.6–7.7 at human 5-HT2B, 7.2–8.6 at human 5-HT2C).[74][36][35] Hallucinogenic compounds like lysergic acid diethylamide (LSD) act as potent agonists with high affinity at 5-HT2A (pKi 9.4, Ki ≈ 0.4 nM), contributing to their psychoactive effects.[74] Antagonists provide tools for dissecting subtype-specific roles, such as ketanserin, a selective 5-HT2A antagonist (pKi 8.1–9.7 at human 5-HT2A, with >50-fold selectivity over 5-HT2B and 5-HT2C), SB-204741, a selective 5-HT2B antagonist (pKi 6.9 at human 5-HT2B, ≥135-fold selective over 5-HT2A and 5-HT2C), and RS-102221, a selective 5-HT2C antagonist (pKi 8.3–8.4 at human 5-HT2C, ~100-fold selective over 5-HT2A and 5-HT2B).[74][36][35][75][76] Inverse agonists, which reduce constitutive receptor activity, include pimavanserin, selective for 5-HT2A (pKi 9.3 at human 5-HT2A, with low affinity at other 5-HT2 subtypes).[74][77]| Ligand | Type | 5-HT2A (human pKi / Ki) | 5-HT2B (human pKi / Ki) | 5-HT2C (human pKi / Ki) | Selectivity Notes |
|---|---|---|---|---|---|
| Serotonin (5-HT) | Endogenous agonist | 6.0–8.4 | 7.9–8.4 | 6.8–8.6 | Non-selective across subtypes[74][36][35] |
| Tryptamine | Trace amine agonist | 5.5–7.6 | ~6.0 (estimated low affinity) | ~6.0 (estimated low affinity) | Weak, non-selective[74] |
| α-Methyl-5-HT | Synthetic agonist | 7.8 | 7.5–8.0 | 6.9–8.6 | Non-selective across subtypes[74][35] |
| DOI | Synthetic agonist | 7.4–9.2 | 7.6–7.7 | 7.2–8.6 | Comparable affinity across subtypes[74][36][35] |
| LSD | Synthetic agonist (hallucinogen) | 9.4 (Ki ≈ 0.4 nM) | 9.0 | 8.2–9.0 | High affinity, non-selective across subtypes[74][36][35] |
| Ketanserin | Synthetic antagonist | 8.1–9.7 | <6.0 | 6.8–7.5 | >50-fold selective for 5-HT2A[74][78] |
| SB-204741 | Synthetic antagonist | <5.2 | 6.9 | 5.6 | ≥135-fold selective for 5-HT2B[36][75] |
| RS-102221 | Synthetic antagonist | ~6.5 | ~6.5 | 8.3–8.4 | ~100-fold selective for 5-HT2C[35][76] |
| Pimavanserin | Inverse agonist | 9.3 (Ki = 0.5 nM) | <6.0 | ~7.0 | Selective for 5-HT2A[74][77] |