首页> 外文期刊>The Journal of Urology >Effect of oral Tadenan treatment on rabbit bladder structure and function after partial outlet obstruction.
【24h】

Effect of oral Tadenan treatment on rabbit bladder structure and function after partial outlet obstruction.

机译:Tadenan口服治疗对部分出口阻塞后兔膀胱结构和功能的影响。

获取原文
获取原文并翻译 | 示例
       

摘要

PURPOSE: There is increasing evidence that the progressive dysfunction induced by partial outlet obstruction is mediated by ischemia-reperfusion, and bladder decompensation results from ischemia-reperfusion induced damage to the cellular and subcellular organelle membranes of nerve and smooth muscle, mitochondria and sarcoplasmic reticulum. Tadenan, an extract of Pygeum africanum, is a therapeutic prescribed in Europe to relieve symptoms of obstructive bladder dysfunction secondary to benign prostatic hyperplasia. There is excellent experimental evidence that Tadenan treatment of obstructed rabbits reduces and reverses the progression of bladder decompensation. We determined whether Tadenan therapy can reverse the morphological damage associated with obstructive dysfunction. MATERIAL AND METHODS: A total of 36 male New Zealand White rabbits were separated into 6 groups of 6 each. Rabbits in groups 1 and 2 underwent sham operation. For 3 weeks beginning 2 weeks after sham operation group 1 was treated with vehicle and group 2 was treated with 30 mg./kg. Tadenan daily. Rabbits in groups 3 to 6 underwent partial outlet obstruction surgery. Two weeks after obstruction each rabbit was treated for 3 weeks with vehicle in group 3, and with 1, 10 and 30 mg./kg. Tadenan in groups 4, 5 and 6, respectively. After the completion of treatment cystometry was performed on each rabbit and isolated bladder strips were evaluated for contractile responses to field stimulation, adenosine triphosphate, carbachol and KCl. Separate strips were fixed for electron microscopy to determine the location and severity of cellular and subcellular membrane damage. RESULTS: Partial outlet obstruction resulted in reduced compliance, decreased responses of bladder strips to all forms of stimulation tested, and significant and extensive damage to cellular and subcellular organelle membranes consistent with an ischemia-reperfusion etiology. Daily 1 and 10 mg./kg. Tadenan treatments had little effect on the obstruction induced increase in bladder weight or the deleterious changes in bladder function and structure. However, treating obstructed rabbits with 30 mg./kg. Tadenan daily resulted in reduced bladder hypertrophy, improved compliance, improved contractile responses to nearly normal levels of isolated bladder strips to all stimuli tested and reversal of obstruction induced structural damage to cellular and subcellular organelle membranes. CONCLUSION: Tadenan treatment of obstructed rabbits resulted in a dose dependent improvement in bladder ultrastructure in parallel with improved bladder compliance and contractile responses of isolated strips to stimulation, providing support for the hypothesis that damage to cellular and subcellular organelle membranes mediates the contractile dysfunction induced by partial outlet obstruction.
机译:目的:越来越多的证据表明,局部出口梗阻引起的进行性功能障碍是由缺血再灌注介导的,并且缺血再灌注引起的神经和平滑肌细胞,细胞膜,线粒体和肌浆网的损伤是膀胱失代偿的结果。 Tadenan是非洲臀果木的提取物,在欧洲已被指定用于缓解继发于前列腺增生症的阻塞性膀胱功能障碍症状的治疗剂。极好的实验证据表明Tadenan治疗阻塞的兔子可减少并逆转膀胱代偿失调的进程。我们确定了Tadenan治疗是否可以逆转与阻塞性功能障碍有关的形态学损害。材料与方法:将36只新西兰大白兔分为6组,每组6只。第1组和第2组的兔子进行假手术。在假手术后2周开始的3周内,第1组用赋形剂治疗,第2组用30mg./kg治疗。塔德南每日。 3至6组的兔子进行部分出口阻塞手术。阻塞后两周,在第3组中用媒介物以1、10和30 mg./kg治疗每只兔子3周。 Tadenan在第4、5和6组中。治疗完成后,对每只兔子进行膀胱测压,并评估离体膀胱条对野外刺激,三磷酸腺苷,卡巴胆碱和KCl的收缩反应。固定单独的条带以进行电子显微镜检查,以确定细胞和亚细胞膜损伤的位置和严重性。结果:部分出口梗阻导致顺应性降低,膀胱条对所有形式的刺激的反应减少,对细胞和亚细胞器细胞膜的重大和广泛损害,这与缺血再灌注病因一致。每天1和10 mg./kg。 Tadenan治疗对梗阻引起的膀胱重量增加或膀胱功能和结构的有害变化影响很小。但是,以30 mg./kg的剂量治疗阻塞的兔子。 Tadenan每天可减少膀胱肥大,改善顺应性,改善对所有测试刺激的接近正常水平的孤立膀胱条的收缩反应,并逆转阻塞引起的对细胞和亚细胞器细胞膜的结构性损伤。结论:Tadenan治疗阻塞性兔子会导致膀胱超微结构的剂量依赖性改善,同时改善膀胱顺应性和离体条带对刺激的收缩反应,为以下假设提供了支持:细胞膜和亚细胞器细胞膜的损伤介导了由C诱导的收缩功能障碍。局部出口阻塞。

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