Drug therapy of overactive bladder--what is coming next?

Korean Journal of Urology Pub Date : 2015-10-01 Epub Date: 2015-10-02 DOI:10.4111/kju.2015.56.10.673
Karl-Erik Andersson
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引用次数: 8

Abstract

After the approval and introduction of mirabegron, tadalafil, and botulinum toxin A for treatment of lower urinary tract symptoms/overactive bladder, focus of interest has been on their place in therapy versus the previous gold standard, antimuscarinics. However, since these agents also have limitations there has been increasing interest in what is coming next - what is in the pipeline? Despite progress in our knowledge of different factors involved in both peripheral and central modulation of lower urinary tract dysfunction, there are few innovations in the pipe-line. Most developments concern modifications of existing principles (antimuscarinics, β3-receptor agonists, botulinum toxin A). However, there are several new and old targets/drugs of potential interest for further development, such as the purinergic and cannabinoid systems and the different members of the transient receptor potential channel family. However, even if there seems to be good rationale for further development of these principles, further exploration of their involvement in lower urinary tract function/dysfunction is necessary.

Abstract Image

膀胱过动症的药物治疗——下一步是什么?
在mirabegron、他达拉非和肉毒杆菌毒素A被批准用于治疗下尿路症状/膀胱过动症后,人们关注的焦点是它们在治疗中的地位,而不是之前的金标准——抗毒蕈素。然而,由于这些代理也有局限性,人们对接下来会发生什么越来越感兴趣——正在筹备中的是什么?尽管我们对涉及下尿路功能障碍的外周和中枢调节的不同因素的了解有所进展,但管道方面的创新很少。大多数发展涉及对现有原理的修改(抗毒蕈素,β3受体激动剂,肉毒杆菌毒素A)。然而,有一些新的和旧的靶点/药物,如嘌呤能和大麻素系统以及瞬时受体电位通道家族的不同成员,具有进一步开发的潜在兴趣。然而,即使这些原理的进一步发展似乎有很好的理由,进一步探索它们与下尿路功能/功能障碍的关系是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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