Serotonin receptor agonist
A serotonin receptor agonist is an
Non-selective agonists
Drugs that increase
5-HT1 receptor agonists
5-HT1A receptor agonists
5-HT1B receptor agonists
Triptans such as sumatriptan, rizatriptan, and naratriptan are 5-HT1B receptor agonists that are used to abort migraine and cluster headache attacks. The ergoline antimigraine agent ergotamine also acts on this receptor.
Serenics such as batoprazine, eltoprazine, and fluprazine are agonists of the 5-HT1B receptor and other serotonin receptors, and have been found to produce antiaggressive effects in animals, but have not been marketed. Eltoprazine is under development for the treatment of aggression and for other indications.[1]
5-HT1D receptor agonists
In addition to being 5-HT1B agonists, triptans (i.e. sumatriptan, almotriptan, zolmitriptan, naratriptan, eletriptan, frovatriptan and rizatriptan) are also agonists at the 5-HT1D receptor, which contributes to their antimigraine effect caused by vasoconstriction of blood vessels in the brain. The same is true for ergotamine.
5-HT1E receptor agonists
The triptan
5-HT1F receptor agonists
Triptans such as eletriptan, naratriptan, and sumatriptan are agonists of the 5-HT1F receptor. Lasmiditan is a selective 5-HT1F agonist that is under development by Eli Lilly and Company for the treatment of migraine.[2][3]
5-HT2 receptor agonists
5-HT2A receptor agonists
Serotonergic psychedelics like psilocybin, LSD, and mescaline act as 5-HT2A receptor agonists. Their actions at this receptor are thought to be responsible for their hallucinogenic effects. Most of these drugs also act as agonists of other serotonin receptors. Not all 5-HT2A receptor agonists are psychoactive.[4]
The 25-NB (NBOMe) series is a family of phenethylamine serotonergic psychedelics that, unlike other classes of serotonergic psychedelics, act as highly selective 5-HT2A receptor agonists.[5] The most well-known member of the 25-NB series is 25I-NBOMe.[6][7] (2S,6S)-DMBMPP is an analogue of the 25-NB compounds and is the most highly selective agonist of the 5-HT2A receptor that has been identified to date.[8] O-4310 (1-isopropyl-6-fluoropsilocin) is a tryptamine derivative that is a highly selective agonist of the 5-HT2A receptor.[9]
Selective 5-HT2A receptor agonists like the 25-NB compounds, specifically those which can behave as full agonists at this receptor, can cause
5-HT2B receptor agonists
Agonists of the 5-HT2B receptor are implicated in the development of cardiac fibrosis.[13] Fenfluramine, pergolide, and cabergoline have been withdrawn from some markets for this reason.[14] Many serotonergic psychedelics, such as LSD and psilocin, have been shown to activate this receptor directly.[15] MDMA has been reported to be both a potent direct agonist[13] and have an indirect effect by increasing plasma serotonin levels.[16]
5-HT2C receptor agonists
5-HT3 receptor agonists
2-Methyl-5-hydroxytryptamine (2-methylserotonin) and quipazine are moderately selective agonists of the 5-HT3 receptor that are used in scientific research. Agonists of this receptor are known to induce nausea and vomiting, and are not used medically.
5-HT4 receptor agonists
Cisapride and tegaserod are 5-HT4 receptor partial agonists that were used to treat disorders of gastrointestinal motility. Prucalopride is a highly selective 5-HT4 receptor agonist that can be used to treat certain disorders of gastrointestinal motility. Other 5-HT4 receptor agonists have shown potential to be nootropic and antidepressant drugs, but have not been marketed for such indications.
5-HT5A receptor agonists
5-HT6 receptor agonists
No selective agonists of the
5-HT7 receptor agonists
AS-19 is a 5-HT7 receptor agonist that has been used in scientific research.
See also
References
- ^ "Eltoprazine - Elto Pharma - AdisInsight".
- S2CID 6034372.
- ^ "Lasmiditan - Eli Lilly and Company - AdisInsight".
- PMID 10432484.
- PMID 28097528.
- S2CID 35219099.
- ^ S2CID 25752763.
- PMID 23336049.
- ^ "Indole compounds useful as serotonin selective agents".
- ^ PMID 25659919.
- S2CID 12179122.
- PMID 23145389.
- ^ a b Hutcheson, J. D., Setola, V., Roth, B. L., & Merryman, W. D. (2011). Serotonin receptors and heart valve disease—it was meant 2B. Pharmacology & Therapeutics, 132(2), 146-157.
- ^ Brea, J., Castro-Palomino, J., Yeste, S., Cubero, E., Párraga, A., Domínguez, E., & Loza, M. I. (2010). Emerging Opportunities and Concerns for Drug Discovery at Serotonin 5-HT2B Receptors. Current Topics in Medicinal Chemistry, 10(5), 493-503.
- ^ Halberstadt, A. L., & Geyer, M. A. (2011). Multiple receptors contribute to the behavioral effects of indoleamine hallucinogens. Neuropharmacology, 61(3), 364-381.
- ^ Zolkowska, D., Rothman, R. B., & Baumann, M. H. (2006). Amphetamine analogs increase plasma serotonin: implications for cardiac and pulmonary disease. Journal of Pharmacology and Experimental Therapeutics, 318(2), 604-610.
- PMID 26099069.
External links
- IUPHAR GPCR Database - 5-HT receptor family
- MeSH list of agents 82017366
- Serotonin+agonists at the U.S. National Library of Medicine Medical Subject Headings (MeSH)