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5-HT(3) Receptors
5-Hydroxytryptamine type 3 (5-HT(3)) receptors are cation-selective Cys loop receptors found in both the central and peripheral nervous systems. There are five 5-HT(3) receptor subunits (A–E), and all functional receptors require at least one A subunit. Regions from noncontiguous parts of the subuni...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Biochemistry and Molecular Biology
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504740/ https://www.ncbi.nlm.nih.gov/pubmed/23038271 http://dx.doi.org/10.1074/jbc.R112.406496 |
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author | Lummis, Sarah C. R. |
author_facet | Lummis, Sarah C. R. |
author_sort | Lummis, Sarah C. R. |
collection | PubMed |
description | 5-Hydroxytryptamine type 3 (5-HT(3)) receptors are cation-selective Cys loop receptors found in both the central and peripheral nervous systems. There are five 5-HT(3) receptor subunits (A–E), and all functional receptors require at least one A subunit. Regions from noncontiguous parts of the subunit sequence contribute to the agonist-binding site, and the roles of a range of amino acid residues that form the binding pocket have been identified. Drugs that selectively antagonize 5-HT(3) receptors (the “setrons”) are the current gold standard for treatment of chemotherapy-induced and postoperative nausea and vomiting and have potential for the treatment of a range of other conditions. |
format | Online Article Text |
id | pubmed-3504740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-35047402012-11-23 5-HT(3) Receptors Lummis, Sarah C. R. J Biol Chem Minireviews 5-Hydroxytryptamine type 3 (5-HT(3)) receptors are cation-selective Cys loop receptors found in both the central and peripheral nervous systems. There are five 5-HT(3) receptor subunits (A–E), and all functional receptors require at least one A subunit. Regions from noncontiguous parts of the subunit sequence contribute to the agonist-binding site, and the roles of a range of amino acid residues that form the binding pocket have been identified. Drugs that selectively antagonize 5-HT(3) receptors (the “setrons”) are the current gold standard for treatment of chemotherapy-induced and postoperative nausea and vomiting and have potential for the treatment of a range of other conditions. American Society for Biochemistry and Molecular Biology 2012-11-23 2012-10-04 /pmc/articles/PMC3504740/ /pubmed/23038271 http://dx.doi.org/10.1074/jbc.R112.406496 Text en © 2012 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles |
spellingShingle | Minireviews Lummis, Sarah C. R. 5-HT(3) Receptors |
title | 5-HT(3) Receptors |
title_full | 5-HT(3) Receptors |
title_fullStr | 5-HT(3) Receptors |
title_full_unstemmed | 5-HT(3) Receptors |
title_short | 5-HT(3) Receptors |
title_sort | 5-ht(3) receptors |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504740/ https://www.ncbi.nlm.nih.gov/pubmed/23038271 http://dx.doi.org/10.1074/jbc.R112.406496 |
work_keys_str_mv | AT lummissarahcr 5ht3receptors |