Wikipedia

5-HT3 antagonist

(Redirected from 5HT-3 antagonist)

The 5-HT3 antagonists, informally known as "setrons", are a class of drugs that act as receptor antagonists at the 5-HT3 receptor, a subtype of serotonin receptor found in terminals of the vagus nerve and in certain areas of the brain. With the notable exceptions of alosetron and cilansetron, which are used in the treatment of irritable bowel syndrome, all 5-HT3 antagonists are antiemetics, used in the prevention and treatment of nausea and vomiting. They are particularly effective in controlling the nausea and vomiting produced by cancer chemotherapy and are considered the gold standard for this purpose.[1]

5-HT3 receptor antagonist
Drug class
Skeletal formula of ondansetron, the prototypical 5-HT3 antagonist
Class identifiers
UseNausea and Vomiting
ATC codeA04AA
Biological target5-HT3 receptor
Clinical data
Drugs.comDrug Classes
Consumer ReportsBest Buy Drugs
External links
MeSHD058831
Legal status
In Wikidata

The 5-HT3 antagonists may be identified by the suffix -setron,[2] and are classified under code A04AA of the WHO's Anatomical Therapeutic Chemical Classification System.

Medical uses

edit

5-HT3 antagonists are most effective in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV), especially that caused by highly emetogenic drugs such as cisplatin; when used for this purpose, they may be given alone or, more frequently, with a glucocorticoid, usually dexamethasone. They are usually given intravenously, shortly before administration of the chemotherapeutic agent,[3] although some authors have argued that oral administration may be preferred.[4] The concomitant administration of a NK1 receptor antagonist, such as aprepitant, significantly increases the efficacy of 5-HT3 antagonists in preventing both acute and delayed CINV.[5]

The 5-HT3 antagonists are also indicated in the prevention and treatment of radiation-induced nausea and vomiting (RINV), when needed, and postoperative nausea and vomiting (PONV). Although they are more effective at controlling CINV—where they stop symptoms altogether in up to 70% of people, and reduce them in the remaining 30%—, they are just as effective as other agents for PONV.

Current evidence suggests that 5-HT3 antagonists are ineffective in controlling motion sickness.[6][7][8] A randomized, placebo-controlled trial of ondansetron to treat motion sickness in air ambulance personnel showed subjective improvement, but it was not statistically significant.[9]

Available agents

edit
  • Ondansetron was the first 5-HT3 antagonist, developed by Glaxo around 1984. Its efficacy was first established in 1987, in animal models,[10][11] and it was extensively studied over the following years.[12] Ondansetron was approved by the U.S. Food and Drug Administration in 1991, and has since become available in several other countries, including the UK, Ireland, Australia, Canada, France and Brazil. As of 2008, ondansetron and granisetron are the only 5-HT3 antagonists available as a generic drug in the United States. Ondansetron may be given several times daily, depending on the severity of symptoms.
  • Tropisetron was also first described in 1984.[13] It is available in several countries, such as the UK, Australia and France, but not in the United States. The effects of tropisetron last up to 24 hours, so it only requires once-daily administration.
  • Granisetron was developed around 1988.[14] It is available in the U.S., UK, Australia and other countries. Clinical trials suggest that it is more effective than other 5-HT3 antagonists in preventing delayed CINV (nausea and vomiting that occur more than 24 hours after the first dose of chemotherapy).[15] It is taken once daily.
  • Dolasetron was first mentioned in the literature in 1989.[16] It is a prodrug, and most of its effects are due to its active metabolite, hydrodolasetron, which is formed in the liver by the enzyme carbonyl reductase. Dolasetron was approved by the FDA in 1997, and is also administered once daily.
  • Palonosetron is the newest 5-HT3 antagonist to become available in the U.S. market. It is an isoquinoline derivative, and is effective in preventing delayed CINV.[17] Palonosetron was approved by the FDA in 2003,[18] initially for intravenous use. An oral formulation was approved on August 22, 2008, for prevention of acute CINV alone, as a large clinical trial did not show oral administration to be as effective as IV use against delayed CINV.[19]
  • Ramosetron is only available in Japan and certain Southeast Asian countries as of 2008.[20] It has higher affinity for the 5-HT3 receptor than the older 5-HT3 antagonists, and maintains its effects over two days; it is therefore significantly more effective for delayed CINV.[21] In animal studies, ramosetron was also effective against irritable bowel syndrome-like symptoms.[22]

Alosetron and cilansetron—the latter was developed by Solvay but never approved by the FDA —are not antiemetics; instead, they are indicated in the treatment of a subset of irritable bowel syndrome where diarrhea is the dominant symptom. Alosetron was withdrawn from the U.S. market in 2000 due to unacceptably frequent severe side effects, including ischemic colitis, and is only available through a restrictive program to patients who meet certain requirements.[23]

Certain prokinetic drugs such as cisapride, renzapride and metoclopramide, although not 5-HT3 antagonists proper, possess some weak antagonist effect at the 5-HT3 receptor. Galanolactone, a diterpenoid found in ginger, is a 5-HT3 antagonist and is believed to at least partially mediate the anti-emetic activity of this plant.[24][25] Mirtazapine is a tetracyclic antidepressant with 5-HT2 and 5-HT3 antagonist effects that also possesses strong anti-emetic properties, however it is also very sedating. Studies show that Mirtazapine is as equally effective in treating chemotherapy-related nausea and vomiting as standard treatments; it is also cheaper and has fewer side effects than typical anti-emetics, and its antidepressant qualities may be an added benefit for cancer populations.[26] Mirtazapine has also been used in the treatment of the motility disorder gastroparesis due to its anti-emetic effects.[27] Olanzapine, an atypical antipsychotic with anti-emetic properties similar to those of mirtazapine, also shows promise in treating chemotherapy-induced nausea and vomiting.[26]

Adverse effects

edit

There are few side effects related to the use of 5-HT3 antagonists; the most common are constipation or diarrhea, headache, and dizziness.[28] Unlike antihistamines with antiemetic properties such as cyclizine, 5-HT3 antagonists do not produce sedation, nor do they cause extrapyramidal effects, as phenothiazines (such as prochlorperazine) sometimes do.

All 5-HT3 antagonists have been associated with asymptomatic electrocardiogram changes, such as prolongation of the PT and QTc intervals and certain arrhythmias.[28] The clinical significance of these side effects is unknown.

Pharmacology

edit

Mechanism of action

edit

The 5-HT3 receptors are present in several critical sites involved in emesis, including vagal afferents, the solitary tract nucleus (STN), and the area postrema itself. Serotonin is released by the enterochromaffin cells of the small intestine in response to chemotherapeutic agents and may stimulate vagal afferents (via 5-HT3 receptors) to initiate the vomiting reflex. The 5-HT3 receptor antagonists suppress vomiting and nausea by inhibiting serotonin binding to the 5-HT3 receptors. The highest concentration of 5-HT3 receptors in the central nervous system (CNS) are found in the STN and chemoreceptor trigger zone (CTZ), and 5-HT3 antagonists may also suppress vomiting and nausea by acting at these sites.[29] The 5-HT3 antagonists are greatly selective and have little affinity for other receptors, such as dopamine, histamine and muscarinic acetylcholine receptors.[28]

Pharmacokinetics

edit

All 5-HT3 antagonists are well-absorbed and effective after oral administration,[4][28] and all are metabolized in the liver by various isoenzymes of the cytochrome P450 system. They do not, however, inhibit or induce these enzymes.[28]

Comparative pharmacology

edit

Despite that the 5-HT3 receptor antagonists share their mechanism of action, they have different chemical structures and exhibit differences in affinity for the receptor, dose response and duration of effect. They are also metabolized in different ways, that is, different components of the cytochrome P450 (CYP) system predominate in the metabolism of the antagonists.[30]

Because of this, patients who are resistant to one antagonist might benefit from another. A correlation exists between the number of active CYP 2D6 alleles and the number of vomiting episodes by patients who receive treatment with cisplatin and ondansetron or tropisetron. Patients with multiple alleles tend to be unresponsive to the antiemetic drug and vice versa.[31]

Comparative pharmacology of 5-HT3 receptor antagonist[29]
Drug Chemical
nature 		Receptor antagonists T1/2 (h) Metabolism Dose
Ondansetron Carbazole derivative 5-HT3 receptor antagonist and weak 5-HT4 antagonist 3.9 hours CYP1A1/2, CYP2D6, CYP 3A3/4/5 150  μg/kg
Granisetron Indazole 5-HT3 receptor antagonist 9–11.6 hours CYP3A3/4/5 10  μg/kg
Dolasetron Indole 5-HT3 receptor antagonist 7–9 hours CYP 3A3/4/5, CYP2D6 600 – 3000  μg/kg
Palonosetron Isoquinoline 5-HT3 receptor antagonist; highest affinity for 5-HT3 receptor in this class 40 hours CYP1A2, CYP2D6, CYP3A3/4/5[32] 0.25  mg dose
Ramosetron Benzimidazole derivative 5-HT3 receptor antagonist 5.8 hours 300  μg/kg
Tropisetron[30] Indole 5-HT3 receptor antagonist 5.6 hours CYP 3A3/4/5, CYP2D6 200  μg/kg
Vortioxetine (Trintellix) Indole 5-HT3 receptor antagonist Antidepressant 66h CYP 2D6/ 2A6/CYP2B6/CYP2C8/9, CYP2C19 5  mg, 10  mg, 20  mg doses

History

edit

The history of the 5-HT3 receptor antagonists began in 1957, when John Gaddum and Zuleika P. Picarelli at the University of Edinburgh proposed the existence of two serotonin receptor subtypes, the M and D receptors (thus named because their function could be blocked by morphine and dibenzyline respectively).[33] The 5-HT3 receptor was later found to correspond to the M receptor.[34] In the 1970s, John Fozard found that metoclopramide and cocaine were weak antagonists at the 5-HT3 (5-HT-M) receptor. Fozard and Maurice Gittos later synthesized MDL 72222, the first potent and truly selective 5-HT3 receptor antagonist.[35][36] The antiemetic effects of metoclopramide were found to be partially because of its serotonin antagonism.[30]

While Fozard was investigating cocaine analogues, researchers at Sandoz identified the potent, selective 5-HT3 receptor antagonist ICS 205-930 from which the first marketed selective 5-HT3 receptor antagonists ondansetron and granisetron were developed, and approved in 1991 and 1993 respectively.[35][37] Several compounds related to MDL 72222 were synthesized which eventually resulted in approval of tropisetron in 1994 and dolasetron in 1997.[37] A new and improved 5-HT3 receptor antagonist, named palonosetron, was approved in 2003.[37] The development of selective 5-HT3 receptor antagonists was a dramatic improvement in the treatment of nausea and vomiting.[30] Ondansetron, granisetron, dolasetron and palonosetron are currently approved in the United States, and form the cornerstone of therapy for the control of acute emesis with chemotherapy agents with moderate to high emetogenic potential.[38]

Development

edit

5-HT3 receptor antagonists or serotonin antagonists were first introduced in the early 1990s, and they have become the most widely used antiemetic drugs in chemotherapy.[29] They have also been proven safe and effective for treatment of postoperative nausea and vomiting.[30] Serotonin (5-HT) is found widely distributed throughout the gut and the central nervous system. In the gut, 5-HT is found mostly in mucosal enterochromaffin cells. Enterochromaffin cells are sensory transducers that release 5-HT to activate intrinsic (via 5-HT1P and 5-HT4 receptors) and extrinsic (via 5-HT3 receptors) primary afferent nerves.[39] Chemotherapeutic drugs for malignant disorders that cause vomiting have been found to cause release of large amounts of serotonin from enterochromaffin cells in the gut, serotonin acts on 5-HT3 receptors in the gut and brain stem.[39]

Drug design

edit

Experiments have shown evidence that the ligand-binding site is located at the interface of two adjacent subunits.[40] The ligand binding site is formed by three loops (A-C) from the principal ligand binding subunit (principal face) and three β-strands (D-F) from the adjacent subunit (complementary face).[34][41] The amino acid residue E129 on loop A faces into the binding pocket and forms a critical hydrogen bond with the hydroxyl group of 5-HT. Loop B contains W183, a critical tryptophan ligand binding residue that contributes to a cation-π interaction between the pi electron density of tryptophan and the primary amine of 5-HT. Loop C residues have been considered as candidates for the differing pharmacology of rodent and human 5-HT3 receptors because of their divergence between species. The most important aromatic residue within loop C is probably Y234 that lies opposite to the loop B tryptophan in the ligand binding pocket and is involved in ligand binding. Loops D and F are in fact β-strands not loops. W90 in loop D is critical for ligand binding and antagonists may directly contact R92. The azabicyclic ring of the competitive antagonist granisetron is located close to W183 forming a cation-pi interaction.[42] Loop E residues Y143, G148, E149, V150, Q151, N152, Y153 and K154 may be important for granisetron binding. The structure of loop F has yet to be clarified but W195 and D204 seem to be critical for ligand binding.[34]

Binding affinity of 5-HT3 receptor antagonist[43]
5-HT3 receptor antagonists Binding affinity (Kd, Ki, K50) Species
Tropisetron 11 nM Human
Granisetron 1.44 nM Human
Ondansetron 4.9 nM Human
Palonosetron 31.6 nM Rat cerebral cortex, rabbit ileal myenteric plexus, guinea-pig ileal plexus
Dolasetron 20.03 nM NG 108-15
Metoclopramide (non-selective) 355 nM Human
Cocaine 2.45-83 nM Rat-rabbit

Pharmacophore scaffold

edit
 
Fig 1. Ondansetron: First generation 5-HT3 receptor antagonist
 
Fig 2. Palonosetron: Second generation 5-HT3 receptor antagonist

Chemical structures of the first generation 5-HT3 receptor antagonist can be categorized to three main classes[30]

  1. Carbazole derivatives (ondansetron)
  2. Indazoles (Granisetron)
  3. Indoles (Tropisetron and Dolasetron)

The first-generation 5-HT3 receptor antagonist (ondansetron, dolasetron, granisetron, and tropisetron) have been the most important drugs in antiemetic therapy for emetogenic chemotherapy. They are especially effective in treating acute emesis, occurring in the first 24 hours following chemotherapy.[38] A newer drug palonosetron is a pharmacologically distinct and highly selective, second generation 5-HT3 receptor antagonist.[44] Palonosetron has two stereogenic centers and exists as four stereoisomers.[44] Palonosetron has longer half-life (40h) and greater receptor binding affinity (>30 fold; when compared to first generation antagonists).[38]

Pharmacophore

edit
 
Fig 3. The 5-HT3 receptor antagonists pharmacophore (schematic)

The pharmacophore of 5-HT3receptors consists of three components: a carbonyl-containing linking moiety, aromatic/heteroaromatic ring, and a basic center. The carbonyl group is coplanar to the aromatic ring. 5-HT3 receptor antagonists are more likely to bind in their protonated form.[45] Docking of a range of antagonists into a homology model of the 5-HT3 receptor binding site shows a reasonably good agreement with the pharmacophore model and supports the observed differences between species. Studies of granisetron in the binding pocket revealed that the aromatic rings of granisetron lie between W183 and Y234 and the azabicyclic ring between W90 and F226. In this study another energetically favorable location of granisetron was identified, closer to the membrane, on a position that could be a part of a binding/unbinding pathway for the ligand. A similarly located alternative binding site for granisetron has since been identified in another study of the 5-HT3 receptor.[43]

Structure-activity relationship

edit
 
Fig 4. The main pharmacophoric elements of the known 5-HT3 antagonist

5-HT3 receptor antagonists share the same pharmacophore.[43] An aromatic moiety (preferably indole), a linking acyl group capable of hydrogen bonding interactions, and a basic amine (nitrogen) can be regarded as the key pharmacophoric elements of the known 5-HT3receptor antagonists. There are steric limitations of the aromatic binding site and although two hydrogen-bonding interactions are possible on the heterocyclic linking group (oxadiazole capable of accepting two hydrogen bonds), only one is essential for high affinity. An optimal environment of the basic nitrogen is when its constrained within an azabicyclic system with the highest affinity observed for systems with nitrogen at the bridgehead position and secondary amines being more potent.[46] The 5-HT3 receptor can only accommodate small substituents on the charged amine, a methyl group being optimal.[43] The optimal distance between the aromatic binding site and the basic amine is 8,4-8,9 Å and it is best if a two-carbon linkage separates the oxadiazole and the nitrogen. An increasing substitution of R increases affinity.[46] The most potent antagonists of 5-HT3 receptors have a 6-membered aromatic ring, and they usually have 6,5 heterocyclic rings.[43] No correlation has been found between the lipophilicity of compounds and the 5-HT3 receptor affinities.[47] Since most of the known 5-HT3 antagonists are ester or amide derivatives they are potentially susceptible to hydrolysis, which could be avoided by incorporating H-bond acceptors within a 5-membered heteroaromatic ring.[46]

 
Fig 5. The importance of C5 (R1) and C7 (R2) substitution has been studied

Structure-activity relationship (SAR) studies of LGIC receptor ligands are valuable to investigate their structure and function. An antagonist-like molecule with low intrinsic activity (ia) decreases the frequency of channel-opening and the permeability of ions. Small lipophilic C5 (R1) (see fig. 5) substituents afford compounds with potent antagonism which indicates that the C5 substituent may fit in a narrow, hydrophobic groove of the binding region in the receptor. It seems that the amino acid residues that interact with the C7 (R2) substituents have little to do with ligand binding but play a big role in ion channel gating. Sterically bulky substituents show a greater interaction with the gating amino acid residues and favor the open conformation of the ion channel because of sterical repulsion.[48]

 
Fig 6. The carbonyl group is completely coplanar with the adjacent aromatic ring

Ondansetron is a racemate but the stereochemistry of the asymmetric carbon atom is not an important factor in the 5-HT3 receptor interaction. Annelation of the 1,7-positions of the indole nucleus of ondansetron results in increased affinity for the receptor.[49]

A methyl- group appears to be as effective functionally as a chlorine in the R position (see fig. 6). The carbonyl group is responsible for a strong interaction with the receptor and contributes significantly to the binding process. This carbonyl group is completely coplanar with the adjacent aromatic ring, indicating that the receptor-bound conformation corresponds to one of the most stable conformations of this group in the flexible compounds.[45]

Research

edit

A small, open-label trial carried out in 2000 found ondansetron to be useful in treating antipsychotic-induced tardive dyskinesia in people with schizophrenia.[50][51] The study's patients also showed significant improvement in the disease's symptoms; a later double-blind, randomized controlled trial also found ondansetron to significantly improve schizophrenia symptoms when used as an adjunct to haloperidol, and people taking both drugs experienced fewer of the adverse effects commonly associated with haloperidol.[52]

See also

edit

References

edit
  1. ^ de Wit R, Aapro M, Blower PR (2005). "Is there a pharmacological basis for differences in 5-HT3-receptor antagonist efficacy in refractory patients?". Cancer Chemother Pharmacol. 56 (3): 231–8. doi:10.1007/s00280-005-1033-0. PMID 15838653. S2CID 27576150.
  2. ^ World Health Organization (2006). "The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances" (PDF). (703 KiB). Geneva: WHO Press. Retrieved on 2007-05-15.
  3. ^ Herrstedt, J.; Aapro, M. S.; Roila, F.; Kataja, V. V.; ESMO Guidelines Task Force (2005). ""ESMO Minimum Clinical Recommendations for prophylaxis of chey-induced nausea and vomiting (NV)"". Annals of Oncology. 16: i77–i79. doi:10.1093/annonc/mdi805. PMID 15888767.
  4. ^ a b Lindley C, Blower P (2000). "Oral serotonin type 3-receptor antagonists for prevention of chemotherapy-induced emesis". Am J Health-Syst Pharm. 57 (18): 1685–97. doi:10.1093/ajhp/57.18.1685. PMID 11006796. Free full text with registration at Medscape
  5. ^ Roila F, Fatigoni S (2006). "New antiemetic drugs". Ann Oncol. 17 (Suppl 2): ii96–100. doi:10.1093/annonc/mdj936. PMID 16608997.
  6. ^ Stott JR, Barnes GR, Wright RJ, Ruddock CJ (1989). "The effect on motion sickness and oculomotor function of GR 38032F, a 5-HT3-receptor antagonist with anti-emetic properties". British Journal of Clinical Pharmacology. 27 (2): 147–57. doi:10.1111/j.1365-2125.1989.tb05345.x. PMC 1379774. PMID 2523720.
  7. ^ Levine ME, Chillas JC, Stern RM, Knox GW (2000). "The effects of serotonin (5-HT3) receptor antagonists on gastric tachyarrhythmia and the symptoms of motion sickness". Aviat Space Environ Med. 71 (11): 1111–4. PMID 11086664.
  8. ^ Muth ER, Elkins AN (July 2007). "High dose ondansetron for reducing motion sickness in highly susceptible subjects". Aviat Space Environ Med. 78 (7): 686–92. PMID 17679566.
  9. ^ Dula D, Rosenbach S (2006). "A randomized clinical trial comparing ondansetron with placebo in aeromedical personel with motion sickness". Paper presented at the annual meeting of the National Association of EMS Physicians, Registry Resort, Naples, FL, January 19–21, 2006. Retrieved on April 25, 2009.
  10. ^ Hagan RM, Butler A, Hill JM, Jordan CC, Ireland SJ, Tyers MB (1987). "Effect of the 5-HT3 receptor antagonist, GR38032F, on responses to injection of a neurokinin agonist into the ventral tegmental area of the rat brain". Eur. J. Pharmacol. 138 (2): 303–5. doi:10.1016/0014-2999(87)90450-X. PMID 2442006.
  11. ^ Costall B, Gunning SJ, Naylor RJ, Tyers MB (1987). "The effect of GR38032F, novel 5-HT3-receptor antagonist on gastric emptying in the guinea-pig". Br. J. Pharmacol. 91 (2): 263–4. doi:10.1111/j.1476-5381.1987.tb10280.x. PMC 1853517. PMID 2955843.
  12. ^ See Eur J Cancer Clin Oncol 1989; 25 Suppl 1.
  13. ^ Donatsch P, Engel G, Richardson BP, Stadler PA (1984). "A highly selective and potent antagonist at peripheral neuronal 5-hydroxy tryptamine receptors". Br J Pharmacol 81: 34P.
  14. ^ Zussman BD, Clarkeson A, Coates PE, Rapeport WG (1988). "The pharmacokinetic profile of BRL 43694, a novel 5-HT3 receptor antagonist, in healthy male volunteers". Br J Clin Pharmacol 25: 107P.
  15. ^ Aapro M (2004). "Granisetron: an update on its clinical use in the management of nausea and vomiting". Oncologist. 9 (6): 673–86. doi:10.1634/theoncologist.9-6-673. PMID 15561811. Free full text
  16. ^ Sorensen SM, Humphreys TM, Palfreyman MG (1989). "Effect of acute and chronic MDL 73,147EF, a 5-HT3 receptor antagonist, on A9 and A10 dopamine neurons". Eur. J. Pharmacol. 163 (1): 115–8. doi:10.1016/0014-2999(89)90402-0. PMID 2744086.
  17. ^ De Leon A (2006). "Palonosetron (Aloxi): a second-generation 5-HT3 receptor antagonist for chemotherapy-induced nausea and vomiting". Proceedings (Baylor University. Medical Center). 19 (4): 413–6. doi:10.1080/08998280.2006.11928210. PMC 1618755. PMID 17106506.
  18. ^ "FDA Approves Aloxi (Palonosetron) For Treatment of Chemotherapy-Related Nausea and Vomiting" (Press release). Doctor's Guide Publishing Limited. July 28, 2003. Retrieved 2007-05-15.
  19. ^ Waknine, Yael (September 4, 2008). "FDA Approvals: Nplate, Aloxi, Vidaza". Medscape. Archived from the original on December 2, 2008. Retrieved 2008-09-04. Freely available with registration.
  20. ^ Abridged prescribing information - Nasea (MIMS Philippines)[permanent dead link‍]. Retrieved on June 13, 2008.
  21. ^ Rabasseda X (February 2002). "Ramosetron, a 5-HT3 receptor antagonist for the control of nausea and vomiting". Drugs of Today. 38 (2): 75–89. doi:10.1358/dot.2002.38.2.820104. PMID 12532186.
  22. ^ Hirata T, Funatsu T, Keto Y, Nakata M, Sasamata M (February 2007). "Pharmacological profile of ramosetron, a novel therapeutic agent for IBS". Inflammopharmacology. 15 (1): 5–9. doi:10.1007/s10787-006-1537-1. PMID 17323187. S2CID 29179265.
  23. ^ GlaxoSmithKline (2005). "Lotronex Prescribing Information" (PDF). (203 KiB). U.S. Food and Drug Administration. Retrieved on 2009-07-30.
  24. ^ Ku, Valerie (2003). Ginger[permanent dead link‍]. University of Colorado at Denver and Health Sciences Center School of Pharmacy. Retrieved on 2007-10-25.
  25. ^ Huang QR; Iwamoto M; Aoki S; et al. (1991). "Anti-5-hydroxytryptamine3 effect of galanolactone, diterpenoid isolated from ginger". Chem Pharm Bull. 39 (2): 397–9. doi:10.1248/cpb.39.397. PMID 2054863.
  26. ^ a b Kast R E; Foley, KF (2007). "Cancer chemotherapy and cachexia: mirtazapine and olanzapine are 5-HT3 antagonists with good antinausea effects". European Journal of Cancer Care. 16 (4): 351–354. doi:10.1111/j.1365-2354.2006.00760.x. PMID 17587360.[dead link‍]
  27. ^ Kim S; Shin, IS; Kim, JM; Kang, HC; Mun, JU; Yang, SJ; Yoon, JS (2006). "Mirtazapine for Severe Gastroparesis Unresponsive to Conventional Prokinetic Treatment". Psychosomatics. 47 (5): 440–442. doi:10.1176/appi.psy.47.5.440. PMID 16959934.
  28. ^ a b c d e "5-Hydroxytryptamine3 (5-HT3) Receptor Antagonists" (PDF). Oregon State University College of Pharmacy. 2003. Archived from the original (PDF) on 2013-03-13. Retrieved 2007-05-15.
  29. ^ a b c Brunton, Laurence L.; Lazo, John S.; Parker, Keith L. (2006). Goddman & Gilman's The Pharmacological Basis of Therapeutics. New York: McGraw-Hill. pp. 1000–3. ISBN 978-0-07-142280-2.
  30. ^ a b c d e f Gan TJ (2005). "Selective serotonin 5-HT3 receptor antagonists for postoperative nausea and vomiting: are they all the same?". CNS Drugs. 19 (3): 225–38. doi:10.2165/00023210-200519030-00004. PMID 15740177. S2CID 23209789.
  31. ^ Sanger GJ (September 2008). "5-hydroxytryptamine and the gastrointestinal tract: where next?". Trends in Pharmacological Sciences. 29 (9): 465–71. doi:10.1016/j.tips.2008.06.008. PMID 19086255.
  32. ^ Aapro M (2005). "5-HT(3)-receptor antagonists in the management of nausea and vomiting in cancer and cancer treatment". Oncology. 69 (2): 97–109. doi:10.1159/000087979. PMID 16131816. S2CID 71759860.
  33. ^ GADDUM JH, PICARELLI ZP (September 1957). "Two kinds of tryptamine receptor". British Journal of Pharmacology and Chemotherapy. 12 (3): 323–8. doi:10.1111/j.1476-5381.1957.tb00142.x. PMC 1509685. PMID 13460238.
  34. ^ a b c Barnes NM, Hales TG, Lummis SC, Peters JA (January 2009). "The 5-HT3 receptor--the relationship between structure and function". Neuropharmacology. 56 (1): 273–84. doi:10.1016/j.neuropharm.2008.08.003. PMC 6485434. PMID 18761359.
  35. ^ a b King, Frank D.; Jones, Brian J.; Sanger, Gareth J. (1993). 5-Hydroxytryptamine-3 Receptor Antagonists. CRC Press. pp. 2–3. ISBN 978-0-8493-5463-2.
  36. ^ Galvan, M.; Gittos, M.; Fatmi, M. (October 1996). "DISCOVERY OF 5-HT3 RECEPTOR ANTAGONISTS AND DOLASETRON MESILATE". EJHP Journal (6): 10–11. Archived from the original on 2011-07-20. Retrieved 2010-01-06.
  37. ^ a b c Billio, Atto; Clarke, Mike J.; Morello, Enrico; Billio, Atto (2006). Billio, Atto (ed.). "Comparison of clinical efficacy of serotonin receptor antagonists in highly emetogenic chemotherapy". Cochrane Database of Systematic Reviews (4). doi:10.1002/14651858.CD006272.
  38. ^ a b c Oo TH, Hesketh PJ (April 2005). "Drug insight: New antiemetics in the management of chemotherapy-induced nausea and vomiting". Nature Clinical Practice Oncology. 2 (4): 196–201. doi:10.1038/ncponc0132. PMID 16264934. S2CID 20464189.
  39. ^ a b Kamm MA (March 2002). "Review article: the complexity of drug development for irritable bowel syndrome". Alimentary Pharmacology & Therapeutics. 16 (3): 343–51. doi:10.1046/j.1365-2036.2002.01185.x. PMID 11876686. S2CID 24133545.
  40. ^ Zhu LP, Ye DY, Tang Y (January 2007). "Structure-based 3D-QSAR studies on thiazoles as 5-HT3 receptor antagonists". Journal of Molecular Modeling. 13 (1): 121–31. doi:10.1007/s00894-006-0131-1. PMID 16953442. S2CID 30877434.
  41. ^ Reeves DC, Lummis SC (2002). "The molecular basis of the structure and function of the 5-HT3 receptor: a model ligand-gated ion channel (review)". Molecular Membrane Biology. 19 (1): 11–26. doi:10.1080/09687680110110048. PMID 11989819. S2CID 36985954.
  42. ^ Duffy NH, Lester HA, Dougherty DA (2007). "Ondansetron and Granisetron Binding Orientation in the 5-HT3 Receptor Determined by Unnatural Amino Acid Mutagenesis". ACS Chemical Biology. 7 (10): 1738–45. doi:10.1021/cb300246j. PMC 3477246. PMID 22873819.
  43. ^ a b c d e Thompson AJ, Lummis SC (2006). "5-HT3 Receptors". Current Pharmaceutical Design. 12 (28): 3615–30. doi:10.2174/138161206778522029. PMC 2664614. PMID 17073663.
  44. ^ a b Tian K, Chen H, Tang J, Chen X, Hu Z (November 2006). "Enantioseparation of palonosetron hydrochloride by micellar electrokinetic chromatography with sodium cholate as chiral selector". Journal of Chromatography A. 1132 (1–2): 333–6. doi:10.1016/j.chroma.2006.08.090. PMID 16999973.
  45. ^ a b Hibert MF, Hoffmann R, Miller RC, Carr AA (June 1990). "Conformation-activity relationship study of 5-HT3 receptor antagonists and a definition of a model for this receptor site". Journal of Medicinal Chemistry. 33 (6): 1594–600. doi:10.1021/jm00168a011. PMID 2342053.
  46. ^ a b c Swain CJ; Baker R; Kneen C; et al. (January 1991). "Novel 5-HT3 antagonists. Indole oxadiazoles". Journal of Medicinal Chemistry. 34 (1): 140–51. doi:10.1021/jm00105a021. PMID 1992112.
  47. ^ Cappelli A; Donati A; Anzini M; et al. (August 1996). "Molecular structure and dynamics of some potent 5-HT3 receptor antagonists. Insight into the interaction with the receptor". Bioorganic & Medicinal Chemistry. 4 (8): 1255–69. doi:10.1016/0968-0896(96)00122-8. PMID 8879547.
  48. ^ Yoshida S, Watanabe T, Sato Y (May 2007). "Regulatory molecules for the 5-HT3 receptor ion channel gating system". Bioorganic & Medicinal Chemistry. 15 (10): 3515–23. doi:10.1016/j.bmc.2007.02.054. PMID 17391967.
  49. ^ van Wijngaarden I; Hamminga D; van Hes R; et al. (November 1993). "Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1,7-annelated indole derivatives". Journal of Medicinal Chemistry. 36 (23): 3693–9. doi:10.1021/jm00075a026. PMID 8246239.
  50. ^ Zullino DF, Eap CB, Voirol P (2001). "Ondansetron for tardive dyskinesia". Am J Psychiatry. 158 (4): 657–8. doi:10.1176/appi.ajp.158.4.657-a. PMID 11282718.
  51. ^ Sirota P, Mosheva T, Shabtay H, Giladi N, Korczyn AD (2000). "Use of the selective serotonin 3 receptor antagonist ondansetron in the treatment of neuroleptic-induced tardive dyskinesia". Am J Psychiatry. 157 (2): 287–9. doi:10.1176/appi.ajp.157.2.287. PMID 10671405. Free full text
  52. ^ Zhang ZJ, Kang WH, Li Q, Wang XY, Yao SM, Ma AQ (2006). "Beneficial effects of ondansetron as an adjunct to haloperidol for chronic, treatment-resistant schizophrenia: a double-blind, randomized, placebo-controlled study". Schizophrenia Research. 88 (1–3): 102–10. doi:10.1016/j.schres.2006.07.010. PMID 16959472. S2CID 24911372.
Retrieved from "https://en.wikipedia.org/w/index.php?title=5-HT3_antagonist&oldid=1259229764"