期刊
AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL
卷 176, 期 1-2, 页码 70-77出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.autneu.2013.02.020
关键词
Distigmine; In vitro contractility; Krebs; Smooth muscle strips
资金
- Astellas Pharma
This study evaluated the effects of a 5-HT4 agonist, cisapride, on neuronally evoked smooth muscle responses in bladder, urethra and ileum and compared these effects with those of an acetylcholinesterase inhibitor, distigmine. Electrical field stimulation (EFS) was applied to human bladder and ileum smooth muscle strips from human organ transplant donors and to urethral strips from prostatectomy patients, to evoke neuronally mediated smooth muscle responses. EFS induced contractions in bladder and mixed responses, consisting of contractions and relaxations, in urethra and ileum. Relaxations were mediated by nitric oxide while contractions were partially cholinergic (i.e. atropine sensitive). This atropine sensitive component amounted to similar to 95% in bladder and similar to 75% in ileum, and it was enhanced by distigmine in a concentration dependent manner (0.1-3 mu M; similar to 100-600% increase in bladder and similar to 50-250% increase in ileum). Cisapride (0.0003-1 mu M) also enhanced bladder contractions (similar to 75-100% increase) but had no effect on urethral contractions or relaxations, and modestly enhanced ileum contractions (similar to 10-40% increase). Facilitatory effects of cisapride were reversed by the specific 5-HT4 receptor antagonist, SB-203186 (3 mu M), but were resistant to repeated washing in the bladder. These data indicate that 5-HT4 receptor agonists enhanced EFS-induced contractions in bladder and ileum without an effect on urethra and suggest that it may be possible to enhance bladder activity with a dose of cisapride that is at, or below, those producing gastrointestinal (GI) effects. Although distigmine's maximal facilitation of bladder and GI tract function was greater than that of cisapride, at clinically relevant concentrations cisapride showed much greater efficacy. (C) 2013 Elsevier B.V. All rights reserved.
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