The Full Wiki

5-HT3 receptor: Wikis

Advertisements
  

Note: Many of our articles have direct quotes from sources you can cite, within the Wikipedia article! This article doesn't yet, but we're working on it! See more info or our list of citable articles.

Encyclopedia

From Wikipedia, the free encyclopedia

5-hydroxytryptamine (serotonin) receptor 3A
Identifiers
Symbol HTR3A
Alt. symbols HTR3
Entrez 3359
HUGO 5297
OMIM 182139
RefSeq NM_000869
UniProt P46098
Other data
Locus Chr. 11 q23.1-23.2
5-hydroxytryptamine (serotonin) receptor 3B
Identifiers
Symbol HTR3B
Entrez 9177
HUGO 5298
OMIM 604654
RefSeq NM_006028
UniProt O95264
Other data
Locus Chr. 11 q23.1
5-hydroxytryptamine (serotonin) receptor 3C
Identifiers
Symbol HTR3C
Entrez 170572
HUGO 24003
OMIM 610121
RefSeq NM_130770
UniProt A2RRR5
Other data
Locus Chr. 3 q27
5-hydroxytryptamine (serotonin) receptor 3D
Identifiers
Symbol HTR3D
Entrez 200909
HUGO 24004
OMIM 610122
RefSeq NM_182537
UniProt Q70Z44
Other data
Locus Chr. 3 q27
5-hydroxytryptamine (serotonin) receptor 3E
Identifiers
Symbol HTR3E
Entrez 285242
HUGO 24005
OMIM 610123
RefSeq NM_182589
UniProt Q495G3
Other data
Locus Chr. 3 q27

The 5-HT3 receptor is a member of the superfamily of ligand-gated ion channels, a superfamily that also includes the neuronal nicotinic acetylcholine receptors (nAChRs), and the inhibitory neurotransmitter receptors for GABA (both GABAA and GABAA receptors) and glycine.[1][2] The 5-HT3 receptor is most closely related by homology to the nicotinic acetylcholine receptor.

The 5-HT3 receptor consists of 5 subunits arranged around a central ion conducting pore, which is permeable to sodium, potassium, and calcium ions. Binding of the neurotransmitter 5-hydroxytryptamine (serotonin) to the 5-HT3 receptor opens the channel, which, in turn, leads to an excitatory response in neurons. The 5-HT3 receptor differs markedly in structure and mechanism from the other 5-HT receptor subtypes, which are all G-protein-coupled.

Contents

Structure

As with other ligand gated ion channels, the 5-HT3 receptor is composed of five subunits pseudo symmetrically arranged about a central ion conducting pore. These subunits are proteins encoded by the HTR3A, HTR3B, HTR3C, HTR3D, and/or HTR3E genes.

A functional channel may be compossed of five identical 5-HT3A subunits (homopentameric) or a mixture of 5-HT3A and one of the other four 5-HT3B,[3][4][5] 5-HT3C, 5-HT3D, or 5-HT3E subunits (heteropentameric).[6] It appears that only the 5-HT3A subunits form functional homopentameric channels. All other subunit subtypes must heteropentamerize with 5-HT3A subunits to form functional channels.

Tissue distribution

The 5-HT3 receptor is expressed throughout the central and peripheral nervous systems and mediates a variety of physiological functions.[2] On a cellular level, it has been shown that postsynaptic 5-HT3 receptors mediate fast excitatory synaptic transmission in rat neocortical interneurons and amygdala, and in ferret visual cortex.[7][8][9] 5-HT3 receptors are also present on presynaptic nerve terminals, where they are thought to mediate or modulate neurotransmitter release.[10][11][12]

Effects

When the receptor is activated to open the ion channel by agonists, the following effects are observed:

Agonists

Agonists for the receptor include:

Antagonists

See also: 5-HT3 receptor antagonist: Drug discovery and development

Antagonists for the receptor (sorted by their respective therapeutic application) include:

Discovery

Identification of the 5-HT3 receptor did not take place until 1986 because of a lack of selective pharmacological tool.[2] However, with the discovery that the 5-HT3 receptor plays a prominent role in chemotherapy- and radiotherapy-induced vomiting, and the concomitant development of selective 5-HT3 receptor antagonists to suppress these side effects aroused intense interest from the pharmaceutical industry[15][16] and therefore the identification of 5-HT3 receptors in cell lines and native tissues quickly followed.[2]

References

  1. ^ Maricq AV, Peterson AS, Brake AJ, Myers RM, Julius D (1991). "Primary structure and functional expression of the 5HT3 receptor, a serotonin-gated ion channel". Science 254 (5030): 432–7. doi:10.1126/science.1718042. PMID 1718042.  
  2. ^ a b c d Yakel, JL (2000), Endo, M; Kurachi, Y; Mishina, M, eds., The 5-HT3 receptor channel: function, activation and regulation in Pharmacology of Ionic Channel Function: Activators and Inhibitors (Handbook of Experimental Pharmacology), 147, Berlin: Springer-Verlag, pp. 541–560, ISBN 3540661271  
  3. ^ Davies PA, Pistis M, Hanna MC, Peters JA, Lambert JJ, Hales TG, Kirkness EF (1999). "The 5-HT3B subunit is a major determinant of serotonin-receptor function". Nature 397 (6717): 359–63. doi:10.1038/16941. PMID 9950429.  
  4. ^ Dubin AE, Huvar R, D'Andrea MR, Pyati J, Zhu JY, Joy KC, Wilson SJ, Galindo JE, Glass CA, Luo L, Jackson MR, Lovenberg TW, Erlander MG (1999). "The pharmacological and functional characteristics of the serotonin 5-HT3A receptor are specifically modified by a 5-HT3B receptor subunit". J Biol Chem 274 (43): 30799–810. doi:10.1074/jbc.274.43.30799. PMID 10521471.  
  5. ^ Monk SA, Desai K, Brady CA, Williams JM, Lin L, Princivalle A, Hope AG, Barnes NM (2001). "Generation of a selective 5-HT3B subunit-recognising polyclonal antibody; identification of immunoreactive cells in rat hippocampus". Neuropharmacology 41 (8): 1013–6. doi:10.1016/S0028-3908(01)00153-8. PMID 11747906.  
  6. ^ Niesler B, Walstab J, Combrink S, Moeller D, Kapeller J, Rietdorf J, Boenisch H, Goethert M, Rappold G, Bruess M (2007). "Characterization of the Novel Human Serotonin Receptor Subunits 5-HT3C, 5- HT3D and 5-HT3E". Mol Pharmacol 71 (Mar 28): Epub ahead of print. doi:10.1124/mol.106.032144. PMID 17392525.  
  7. ^ Férézou I, Cauli B, Hill EL, Rossier J, Hamel E, Lambolez B (2002). "5-HT3 receptors mediate serotonergic fast synaptic excitation of neocortical vasoactive intestinal peptide/cholecystokinin interneurons". J Neurosci 22 (17): 7389–97. PMID 12196560.  
  8. ^ Sugita S, Shen KZ, North RA (1992). "5-hydroxytryptamine is a fast excitatory transmitter at 5-HT3 receptors in rat amygdala". Neuron 8 (1): 199–203. doi:10.1016/0896-6273(92)90121-S. PMID 1346089.  
  9. ^ Roerig B, Nelson DA, Katz LC (1992). "Fast synaptic signaling by nicotinic acetylcholine and serotonin 5-HT3 receptors in developing visual cortex". J Neurosci 17 (21): 199–203. PMID 9334409.  
  10. ^ Rondé P, Nichols RA (1998). "High calcium permeability of serotonin 5-HT3 receptors on presynaptic nerve terminals from rat striatum". J Neurochem 70 (3): 1094–103. doi:10.1046/j.1471-4159.1998.70031094.x. PMID 9489730.  
  11. ^ Rondé P, Nichols RA (1997). "5-HT3 receptors induce rises in cytosolic and nuclear calcium in NG108-15 cells via calcium-induced calcium release". Cell Calcium 22 (5): 357–65. doi:10.1016/S0143-4160(97)90020-8. PMID 9448942.  
  12. ^ van Hooft JA, Vijverberg HP (2000). "5-HT3 receptors and neurotransmitter release in the CNS: a nerve ending story?". Trends Neurosci 23 (12): 605–10. doi:10.1016/S0166-2236(00)01662-3. PMID 11137150.  
  13. ^ a b c d e Rang, H. P. (2003). Pharmacology. Edinburgh: Churchill Livingstone. ISBN 0-443-07145-4.   Page 187
  14. ^ Imanishi N, Iwaoka K, Koshio H, Nagashima SY, Kazuta K, Ohta M, Sakamoto S, Ito H, Akuzawa S, Kiso T, Tsukamoto S, Mase T. New thiazole derivatives as potent and selective 5-hydroxytriptamine 3 (5-HT3) receptor agonists for the treatment of constipation. Bioorganic and Medicinal Chemistry. 2003 Apr 3;11(7):1493-502. PMID 12628674
  15. ^ Thompson AJ, Lummis SC (2006). "5-HT3 receptors". Curr Pharm Des 12 (28): 3615–30. doi:10.2174/138161206778522029. PMID 17073663. http://www.ingentaconnect.com/content/ben/cpd/2006/00000012/00000028/art00005.  
  16. ^ Thompson AJ, Lummis SC (2007). "The 5-HT3 receptor as a therapeutic target". Expert Opin Ther Targets 11 (4): 527–40. doi:10.1517/14728222.11.4.527. PMID 17373882.  

External links

Advertisements

Advertisements






Got something to say? Make a comment.
Your name
Your email address
Message