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Muscarinic receptors and gastrointestinal tract smooth muscle function
- Source :
- Life Sciences. 68:2573-2578
- Publication Year :
- 2001
- Publisher :
- Elsevier BV, 2001.
-
Abstract
- Over the last decade, several lines of evidence have shown that both muscarinic M2 and M3 receptors are postjunctionally expressed in many smooth muscles, including the gastrointestinal tract. Although in vitro data suggests that both receptors are functional in that they inhibit adenylate cyclase activity and activate non-selective cation channels, few studies support a role in vivo. Thus, data from procedures that ablate the signaling pathway of the muscarinic M2 receptor, including receptor antagonism, pertussis toxin pretreatment reveal little effect on gastrointestinal smooth muscle responsiveness to muscarinic agonists. Recently, information from knockout mice, lacking either M2 or M3 receptor, indicate reveal a role for both subtypes. However, the contribution of the M2 receptor appears greater in the ileum than in the urinary bladder. Therapeutically, non-selective, as well as selective M3 receptor antagonists are being clinically studied, although it remains to be shown which is the optimal approach to disorders of smooth muscle motility.
- Subjects :
- medicine.medical_specialty
Colonic Diseases, Functional
Muscarinic Antagonists
Biology
Ion Channels
General Biochemistry, Genetics and Molecular Biology
5-HT7 receptor
Digestive System Physiological Phenomena
Internal medicine
Muscarinic acetylcholine receptor
Muscarinic acetylcholine receptor M5
medicine
Muscarinic acetylcholine receptor M4
Animals
Humans
General Pharmacology, Toxicology and Pharmaceutics
Receptor
Receptor, Muscarinic M3
Receptor, Muscarinic M2
Urinary Bladder Diseases
Muscarinic acetylcholine receptor M3
Muscle, Smooth
Muscarinic acetylcholine receptor M2
General Medicine
Muscarinic acetylcholine receptor M1
Receptors, Muscarinic
Endocrinology
Digestive System
Signal Transduction
Subjects
Details
- ISSN :
- 00243205
- Volume :
- 68
- Database :
- OpenAIRE
- Journal :
- Life Sciences
- Accession number :
- edsair.doi.dedup.....686b838c8bd9840c97dfec40d126ef45
- Full Text :
- https://doi.org/10.1016/s0024-3205(01)01054-2