Back to Search
Start Over
5-HT2B receptors do not modulate sensitivity to colonic distension in rats with acute colorectal hypersensitivity.
- Source :
-
Neurogastroenterology & Motility . May2006, Vol. 18 Issue 5, p343-345. 3p. 1 Graph. - Publication Year :
- 2006
-
Abstract
- The 5-HT4 receptor agonist tegaserod is an effective prokinetic agent that increases gastrointestinal secretion and reduces visceral sensitivity. Tegaserod has both 5-HT4 receptor agonist and 5-HT2B receptor antagonist activity, the latter being a less potent effect of the drug. In a rat model of colonic hypersensitivity, selective 5-HT4 receptor antagonists only partially reversed the antihyperalgesic effect of tegaserod suggesting that non-5-HT4 receptor-mediated mechanisms may also be involved in its overall antihyperalgesic action. The objective of this study was to determine whether 5-HT2B receptors play a role in colonic hypersensitivity. A visceromotor response (VMR) in acutely sensitized animals (intracolonic acetic acid, 0.6%, 1.5 mL) quantified colonic hypersensitivity. Acetic acid produced an increase in the VMR at all distension pressures. However, neither the 5-HT2B receptor agonist BW 723C86, the 5-HT2B antagonist SB204741 or the 5-HT2B/2C antagonist SB 206553 caused any significant inhibition of the VMR. In summary, in the same rodent model in which tegaserod has previously been shown to produce a potent antihyperalgesic effect, 5-HT2B receptors do not appear to mediate colonic hypersensitivity. We conclude that 5-HT2B receptor-mediated mechanisms are unlikely to play a role in the antihyperalgesic action of tegaserod in man. [ABSTRACT FROM AUTHOR]
- Subjects :
- *DRUG receptors
*GASTROINTESTINAL system
*SECRETION
*ALLERGIES
*COLON diseases
Subjects
Details
- Language :
- English
- ISSN :
- 13501925
- Volume :
- 18
- Issue :
- 5
- Database :
- Academic Search Index
- Journal :
- Neurogastroenterology & Motility
- Publication Type :
- Academic Journal
- Accession number :
- 20456508
- Full Text :
- https://doi.org/10.1111/j.1365-2982.2006.00767.x