Morita T, Ando M, Hirano S, Dokita S, Kondo S, Tsuchida S
Department of Urology, Tokyo Medical and Dental University School of Medicine.
Nihon Hinyokika Gakkai Zasshi. 1992 Nov;83(11):1835-40. doi: 10.5980/jpnjurol1989.83.1835.
Tiropramide, a tyrosine derivative, has an antispasmodic effect on the gastrointestinal smooth muscles and it is suggested that the effect is mediated by cAMP. Therefore, we studied the effects of tiropramide on the lower urinary tract smooth muscle functions. In animal experiments, the effects of tiropramide on vesicourethral smooth muscle contraction were investigated and cAMP and cGMP levels following tiropramide administration were measured in the vesicourethral and gastrointestinal smooth muscles. In clinical trials, five healthy volunteers and five patients with neurogenic bladder dysfunction were treated orally with tiropramide 300 mg a day for two weeks and examined for urodynamic parameters before and after tiropramide treatment. Tiropramide significantly inhibited contraction of the vesicourethral smooth muscle and the inhibitory effect upon the bladder was remarkable particularly at the lower concentrations. Tiropramide remarkably increased cAMP level but it had no effect on cGMP level in the bladder at the lower concentrations. Tiropramide at the lower concentrations did not affect cAMP and cGMP levels in the smooth muscles of the urethra, stomach and intestines. In the patients with neurogenic bladder dysfunction treated with tiropramide orally, the urine volume at first desire to void and maximum bladder capacity increased significantly, but the volume of residual urine did not significantly increase. In the healthy volunteers, there were no significant changes in urodynamic parameters. These findings indicate that tiropramide relaxes the urinary bladder smooth muscle via cAMP to increase the urinary bladder capacity.
替罗酰胺是一种酪氨酸衍生物,对胃肠道平滑肌有解痉作用,据推测该作用是由环磷酸腺苷(cAMP)介导的。因此,我们研究了替罗酰胺对下尿路平滑肌功能的影响。在动物实验中,研究了替罗酰胺对膀胱尿道平滑肌收缩的影响,并测量了给予替罗酰胺后膀胱尿道和胃肠道平滑肌中环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)的水平。在临床试验中,5名健康志愿者和5名神经源性膀胱功能障碍患者每天口服300mg替罗酰胺,持续两周,并在替罗酰胺治疗前后检查尿动力学参数。替罗酰胺显著抑制膀胱尿道平滑肌的收缩,尤其是在较低浓度时对膀胱的抑制作用显著。在较低浓度下,替罗酰胺显著提高膀胱中环磷酸腺苷(cAMP)水平,但对环磷酸鸟苷(cGMP)水平无影响。较低浓度的替罗酰胺对尿道、胃和肠道平滑肌中的环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)水平无影响。口服替罗酰胺治疗的神经源性膀胱功能障碍患者,首次排尿欲望时的尿量和最大膀胱容量显著增加,但残余尿量没有显著增加。在健康志愿者中,尿动力学参数没有显著变化。这些发现表明,替罗酰胺通过环磷酸腺苷(cAMP)使膀胱平滑肌松弛,从而增加膀胱容量。