Review article: effects of the 5-HT3 receptor antagonist alosetron on neuromuscular transmission in canine and human intestinal muscle
| Autor: | G. T. Somogyi, O. Bayguinov, Anthony J. Bauer, Kenton M. Sanders, G. Audolfsson, W. H. Schraut, T. Yamamoto |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
medicine.medical_specialty
Hepatology business.industry Gastroenterology Neuromuscular transmission Antagonist Bethanechol medicine.disease Symptomatic relief 5-HT3 Receptor Antagonist Endocrinology Alosetron Internal medicine Medicine Pharmacology (medical) business Acetylcholine Irritable bowel syndrome medicine.drug |
| Zdroj: | Alimentary Pharmacology & Therapeutics. 13:39-47 |
| ISSN: | 0269-2813 |
| DOI: | 10.1046/j.1365-2036.1999.00004.x-i2 |
| Popis: | Background: Currently, therapeutic treatments for irritable bowel syndrome fail to produce significant clinical results. We hypothesized that alosetron, a selective 5-HT3 antagonist, may provide symptomatic relief in irritable bowel syndrome patients through a decrease in the amplitude of gastrointestinal contractions. Aim: To determine the in vitro effect of alosetron on neuromuscular transmission in the canine and human jejunal and colonic muscularis externa. Results: Alosetron diminished electrical field-stimulated (EFS) contractions recorded from muscles of the canine and human small and large intestines. Mechanistically, the diminished EFS response could be explained by the ability of alosetron to decrease the fractional release of 14C-choline radiolabelled acetylcholine evoked by EFS from human jejunal muscle. The inhibition of EFS contractions was not limited to atropine-sensitive events, as non-cholinergic excitatory EFS evoked contractions were also inhibited. Additionally, alosetron at high concentrations (> 30 μm) directly altered bethanechol stimulated contractions. Conclusion: Caution must be used in the interpretation of these data because significant alterations in EFS-induced contractions were only observed with large pharmacological concentrations of alosetron, and the response was not selective for cholinergically-mediated excitatory neuromuscular transmission. |
| Databáze: | OpenAIRE |
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