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Urodynamic effects of a novel EP, receptor antagonist in normal rats and rats with bladder outlet obstruction
Linköping University, Department of Medical and Health Sciences, Clinical Pharmacology. Linköping University, Faculty of Health Sciences. (Lund University Hospital)
2007 (English)In: Journal of Urology, ISSN 0022-5347, E-ISSN 1527-3792, Vol. 177, 1562-1567 p.Article in journal (Refereed) Published
Abstract [en]


Prostaglandin E2 and its EP1 receptor were suggested as endogenous modulators of bladder function in the normal physiological state and under pathophysiological conditions. We investigated if the new EP1 receptor antagonist PF-2907617-02 would influence the regulation of normal micturition in rats, and if it affects bladder function in animals with partial bladder outlet obstruction.

Materials and Methods

The study was performed in normal female Sprague-Dawley rats and in rats with moderate, experimentally induced bladder outlet obstruction 2 weeks in duration. All animals underwent continuous cystometry in the awake state. PF-2907617-02 was given intravenously at doses of 0.1 and 1.0 mg/kg–1 in normal rats, and at 1.0 mg/kg–1 in bladder outlet obstructed animals. In a group of normal rats detrusor overactivity was produced by intravesical instillation of prostaglandin E2.


In normal rats PF-2907617-02 (1 mg/kg–1) significantly increased bladder capacity, micturition volume and the micturition interval but it had no effect on other urodynamic parameters. The lower dose of PF-2907617 (0.1 mg/kg–1) showed no effect. Intravesical prostaglandin E2 (50 μM) induced detrusor overactivity. The antagonist significantly decreased the stimulatory effects of prostaglandin E2 at 0.1 and 1.0 mg/kg–1. In obstructed animals PF-2907617-02 significantly increased the micturition interval but not bladder capacity and residual volume. The drug also decreased the frequency and amplitude of nonvoiding contractions.


EP1 receptor is involved in initiation of the micturition reflex in normal rats and in animals with bladder outlet obstruction. It may also contribute to the generation of detrusor overactivity after bladder outlet obstruction. Thus, EP1 receptor antagonists may have potential as treatment for detrusor overactivity in humans.

Place, publisher, year, edition, pages
2007. Vol. 177, 1562-1567 p.
Keyword [en]
bladder; muscle; smooth; bladder neck obstruction; dinoprostone; rats; Sprague-Dawley
National Category
Medical and Health Sciences
URN: urn:nbn:se:liu:diva-41195DOI: 10.1016/j.juro.2006.11.070Local ID: 55330OAI: diva2:262046
Available from: 2009-10-10 Created: 2009-10-10 Last updated: 2011-08-17

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