Abstract
Serotonin 4 receptors (5-HT(4)Rs) were discovered 15 years ago. They are coded by a very complex gene (700Kb, 38 exons) which generates eight carboxy-terminal variants (a, b, c, d, e, f, g, n). Their sequences differ after position L(358). Another variant is characterized by a 14 residue insertion within the extracellular loop 2. Highly selective potent 5-HT(4) receptor antagonists and partial agonists which cross the blood-brain barrier have been synthesized, but a specific full agonist for brain studies is still missing. Based on physiological and behavioral experiments, 5-HT(4)Rs may be targets to treat cognitive deficits, abdominal pain and feeding disorders. One 5-HT(4)R-directed drug (SL65.0155) is already in phase II to treat patients suffering from memory deficits or dementia.
MeSH terms
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Animals
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Brain / drug effects
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Brain / metabolism
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Central Nervous System Diseases / drug therapy
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Central Nervous System Diseases / physiopathology
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Cloning, Molecular
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Digestive System / drug effects
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Digestive System / metabolism
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Drug Evaluation / methods
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GTP-Binding Proteins / metabolism
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Gastrointestinal Diseases / drug therapy*
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Gastrointestinal Diseases / physiopathology
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Humans
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Immunohistochemistry
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Receptors, Serotonin, 5-HT4 / classification*
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Receptors, Serotonin, 5-HT4 / drug effects*
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Receptors, Serotonin, 5-HT4 / genetics
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Receptors, Serotonin, 5-HT4 / metabolism
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Serotonin Antagonists / pharmacology*
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Serotonin Receptor Agonists / pharmacology*
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Signal Transduction
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Structure-Activity Relationship
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Tissue Distribution
Substances
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Serotonin Antagonists
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Serotonin Receptor Agonists
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Receptors, Serotonin, 5-HT4
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GTP-Binding Proteins