首页> 外文期刊>The Journal of Urology >Improvement in bladder storage function by tamsulosin depends on suppression of C-fiber urethral afferent activity in rats.
【24h】

Improvement in bladder storage function by tamsulosin depends on suppression of C-fiber urethral afferent activity in rats.

机译:坦索罗辛对膀胱存储功能的改善取决于对大鼠C纤维尿道传入活性的抑制。

获取原文
获取原文并翻译 | 示例
       

摘要

PURPOSE: Alpha(1)-blockers improve voiding symptoms by decreasing prostatic and urethral smooth muscle tone. However, to our knowledge the mechanism underlying improvements in storage symptoms is not known. Topical application of prostaglandin E(2) to the rat lower urinary tract stimulates the micturition reflex. Using an animal model we investigated whether the alpha(1)-blocker tamsulosin (Astellas Pharma, Tokyo, Japan) acts on C-fiber afferent activity and, if so, the location of this effect. MATERIALS AND METHODS: To induce desensitization of C-fiber afferent activity resiniferatoxin (0.3 mg/kg) was subcutaneously injected in female Sprague-Dawley rats 2 days before experiments. Simultaneous recordings of urethral pressure and rhythmic bladder pressure were made with the rats under urethane anesthesia. Prostaglandin E(2) (0.4 mg/ml) was continuously administered intravesically or intraurethrally to rats pretreated with resiniferatoxin (resiniferatoxin rats) or rats without pretreatment (nonresiniferatoxin rats). We investigated the effects on the micturition reflex of intravenous (2.2 x 10(-1) to 2.2 x 10(3) nM/kg) or intrathecal (0.001 to 0.1 nmol) administration of tamsulosin. RESULTS: The bladder contraction interval was markedly decreased after intravesical or intraurethral administration of prostaglandin E(2) in nonresiniferatoxin rats but it was unchanged in resiniferatoxin rats. This effect was antagonized by the EP1 receptor antagonist ONO-8711 (6-[(2S,3S)-3-(4-chloro-2-methylphenylsulfonylaminomethyl)-bicyclo[2.2.2]o ctan-2-yl]-5Z-hexenoic acid). Intravenous administration of tamsulosin significantly increased the bladder contraction interval in nonresiniferatoxin rats receiving intraurethral prostaglandin E(2) but it had no effect on nonresiniferatoxin rats receiving intravesical prostaglandin E(2). Intrathecal administration of tamsulosin produced a slight and insignificant increase in the bladder contraction interval in nonresiniferatoxin rats receiving intraurethral prostaglandin E(2). CONCLUSIONS: These results suggest that prostaglandin E(2) enhances the micturition reflex through C-fiber afferents and tamsulosin had an inhibitory effect on the C-fiber urethral afferent nerves, thereby improving bladder storage function.
机译:目的:Alpha(1)受体阻滞剂可通过降低前列腺和尿道平滑肌张力来改善排尿症状。然而,据我们所知,改善存储症状的潜在机制尚不清楚。在大鼠下尿路局部应用前列腺素E(2)刺激排尿反射。使用动物模型,我们调查了α(1)受体阻滞坦索罗辛(Astellas Pharma,东京,日本)是否对C纤维传入活性起作用,如果有的话,这种作用的位置。材料与方法:为了诱导C纤维脱敏,在实验前2天,将雌性树脂毒素(0.3 mg / kg)皮下注射到雌性Sprague-Dawley大鼠中。在氨基甲酸乙酯麻醉下同时记录大鼠的尿道压力和节律性膀胱压力。前列腺素E(2)(0.4 mg / ml)连续经膀胱内或尿道内给药于用树脂虫毒素预处理的大鼠(树脂虫毒素大鼠)或未经预处理的大鼠(非树脂毒素大鼠)。我们调查了坦索罗辛静脉(2.2 x 10(-1)至2.2 x 10(3)nM / kg)或鞘内(0.001至0.1 nmol)给药对排尿反射的影响。结果:非树脂毒素毒素大鼠膀胱内或尿道内注射前列腺素E(2)后,膀胱收缩间隔明显缩短,而树脂毒素毒素大鼠中膀胱收缩间隔未改变。 EP1受体拮抗剂ONO-8711(6-[(2S,3S)-3-(4-氯-2-甲基苯基磺酰基氨基甲基)-双环[2.2.2] o ctan-2-yl] -5Z-己酸)。坦索罗辛的静脉内给药显着增加了接受尿道内前列腺素E(2)的非Resiniferatoxin大鼠的膀胱收缩间隔,但对接受膀胱内前列腺素E(2)的非Reiniferiferatoxin大鼠没有影响。鞘内注射坦索罗辛会使接受尿道内前列腺素E(2)的非树脂毒素患者的膀胱收缩间隔略有增加,但微不足道。结论:这些结果表明前列腺素E(2)通过C纤维传入增强了排尿反射,而坦洛新对C纤维尿道传入神经具有抑制作用,从而改善了膀胱的储存功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号