[Recent insights into the pathogenesis of abdominal symptoms in functional bowel disorders]

Recenti Prog Med. 2007 Feb;98(2):69-73.
[Article in Italian]

Abstract

In the gut, 5-HT acts as a paracrine signalling molecule released by enterochromaffin cells and as a transmitter released by some descending serotonergic interneurons. It has a prominent role in the regulation of motility, vascular tone, secretion and perception both in normal and under certain pathophysiological conditions, such as the carcinoid syndrome and the irritable bowel syndrome (IBS). Serotonin is known to markedly influence bowel function by activating at least five receptor types (5-HT(1,2,3,4,7)). Among all 5-HT receptors, those belonging to the 5-HT3 (a ionotropic receptor) and 5-HT4 (a metabotropic receptor) type are the most extensively studied in gastroenterology, resulting in commercially available (although not worldwide) serotonergic agents for the treatment of IBS and functional dyspepsia. Recently, 5-HT7 receptors have been found to participate in the accommodation process of the circular muscle during the preparatory phase of ileal peristalsis. Since an exaggerated accommodation of the gut wall may contribute to abdominal distension and bloating, 5-HT7 receptor ligands may offer innovative opportunities for the pharmacological treatment of functional bowel disorders.

Publication types

  • Comparative Study
  • English Abstract
  • Review

MeSH terms

  • Animals
  • Disease Models, Animal
  • Dyspepsia / drug therapy
  • Dyspepsia / etiology*
  • Enterochromaffin Cells / physiology
  • Gastrointestinal Agents / pharmacology
  • Gastrointestinal Agents / therapeutic use
  • Gastrointestinal Motility / drug effects
  • Gastrointestinal Motility / physiology*
  • Humans
  • Ileum / physiology
  • Immunohistochemistry
  • Irritable Bowel Syndrome / drug therapy
  • Irritable Bowel Syndrome / metabolism
  • Irritable Bowel Syndrome / physiopathology*
  • Muscle, Smooth / drug effects
  • Muscle, Smooth / metabolism
  • Peristalsis / drug effects
  • Peristalsis / physiology
  • Receptors, Serotonin / drug effects
  • Receptors, Serotonin / physiology*
  • Serotonin / physiology*
  • Serotonin Agents / pharmacology
  • Serotonin Agents / therapeutic use
  • Serotonin Antagonists / pharmacology
  • Serotonin Antagonists / therapeutic use

Substances

  • Gastrointestinal Agents
  • Receptors, Serotonin
  • Serotonin Agents
  • Serotonin Antagonists
  • Serotonin